MATH 225 Chamberlain University SARS CoV 2 Virus Paper

Required Resources

Read/review the following resources for this activity:

OpenStax Textbook: Chapter 2

Lesson

  • Chamberlain University Library
  • Internet
  • Scenario/Summary
  • This week’s lab highlights the use of graphics, distributions, and tables to summarize and interpret data.
  • Deliverables

    The deliverable is a Word document with your answers to the questions posed below based on the article you find.

    Required Software

    Microsoft Word

    Internet access to read articles

    Steps to Complete Week 3 Lab

  • Part 1:
  • Step 1: Your instructor will provide you with a scholarly article.  The article will contain at least one graph and/or table. Summarize the article.
  • Part 2:

    Title your paper: “Review of [Name of Article]”

    State the Author:

    Summarize the article in one paragraph:

    Post a screen shot of a frequency table and/or graph from the article.

    Example:

    Frequency Distribution      ORGraph

    Step 4: Answer the following questions about your table or graph.

    What typeof study is used in the article (quantitative or qualitative)? Explainhow you came to that conclusion.

    What typeof graph or table did you choose for your lab (bar graph, histogram, stem & leaf plot, etc.)? What characteristics make it this type (you should bring in material that you learned in the course)?

    Describethe data displayed in your frequency distribution or graph (consider class size, class width, total frequency, list of frequencies, class consistency, explanatory variables, response variables, shapes of distributions, etc.)

    Draw a conclusion about the data from the graph or frequency distribution in context of the article.

    How else might this data have been displayed? Discuss pros and cons of 2 other presentation options, such as tables or different graphical displays. Why don’t you think those two graphs were not used in this article?

    Sugg et al. BMC Nursing
    (2021) 20:215
    https://doi.org/10.1186/s12912-021-00746-5
    RESEARCH
    Open Access
    Fundamental nursing care in patients with
    the SARS-CoV-2 virus: results from the
    ‘COVID-NURSE’ mixed methods survey into
    nurses’ experiences of missed care and
    barriers to care
    Holly V. R. Sugg1*, Anne-Marie Russell1, Leila M. Morgan1, Heather Iles-Smith2,3, David A. Richards1,4,
    Naomi Morley1, Sarah Burnett1, Emma J. Cockcroft1, Jo Thompson Coon1,5, Susanne Cruickshank6, Faye E. Doris1,
    Harriet A. Hunt1, Merryn Kent1, Philippa A. Logan7, Anne Marie Rafferty8, Maggie H. Shepherd9,10, Sally J. Singh11,12,
    Susannah J. Tooze1 and Rebecca Whear1
    Abstract
    Background: Patient experience of nursing care is associated with safety, care quality, treatment outcomes, costs
    and service use. Effective nursing care includes meeting patients’ fundamental physical, relational and psychosocial
    needs, which may be compromised by the challenges of SARS-CoV-2. No evidence-based nursing guidelines exist
    for patients with SARS-CoV-2. We report work to develop such a guideline. Our aim was to identify views and
    experiences of nursing staff on necessary nursing care for inpatients with SARS-CoV-2 (not invasively ventilated) that
    is omitted or delayed (missed care) and any barriers to this care.
    Methods: We conducted an online mixed methods survey structured according to the Fundamentals of Care
    Framework. We recruited a convenience sample of UK-based nursing staff who had nursed inpatients with SARSCoV-2 not invasively ventilated. We asked respondents to rate how well they were able to meet the needs of SARSCoV-2 patients, compared to non-SARS-CoV-2 patients, in 15 care categories; select from a list of barriers to care;
    and describe examples of missed care and barriers to care. We analysed quantitative data descriptively and
    qualitative data using Framework Analysis, integrating data in side-by-side comparison tables.
    * Correspondence: h.v.r.sugg@exeter.ac.uk
    1
    College of Medicine and Health, University of Exeter, St Luke’s Campus,
    Heavitree Road, Exeter EX1 2LU, UK
    Full list of author information is available at the end of the article
    © The Author(s). 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License,
    which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give
    appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if
    changes were made. The images or other third party material in this article are included in the article’s Creative Commons
    licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons
    licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain
    permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
    The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the
    data made available in this article, unless otherwise stated in a credit line to the data.
    Sugg et al. BMC Nursing
    (2021) 20:215
    Page 2 of 17
    Results: Of 1062 respondents, the majority rated mobility, talking and listening, non-verbal communication,
    communicating with significant others, and emotional wellbeing as worse for patients with SARS-CoV-2. Eight
    barriers were ranked within the top five in at least one of the three care areas. These were (in rank order): wearing
    Personal Protective Equipment, the severity of patients’ conditions, inability to take items in and out of isolation
    rooms without donning and doffing Personal Protective Equipment, lack of time to spend with patients, lack of
    presence from specialised services e.g. physiotherapists, lack of knowledge about SARS-CoV-2, insufficient stock, and
    reluctance to spend time with patients for fear of catching SARS-CoV-2.
    Conclusions: Our respondents identified nursing care areas likely to be missed for patients with SARS-CoV-2, and
    barriers to delivering care. We are currently evaluating a guideline of nursing strategies to address these barriers,
    which are unlikely to be exclusive to this pandemic or the environments represented by our respondents. Our
    results should, therefore, be incorporated into global pandemic planning.
    Keywords: Fundamental nursing care, COVID-19, SARS-CoV-2, Missed care, Survey, Mixed methods
    Background
    Patient experience of care is associated with safety, clinical effectiveness, care quality, treatment outcomes, costs
    and service use [1–5], and nursing care is a key determinant of this experience [6, 7]. Although nurses perform both generalist and specialist roles, all nurses are
    involved in meeting patients’ ‘fundamental’ care needs.
    Defining fundamental care has in the past been a contested area [8], but there is now greater consensus [9] in
    that fundamental care can be described as ‘actions on
    the part of the nurse that respect and focus on a person’s essential needs to ensure their physical and psychosocial wellbeing’ ( [9], p.2292). These needs are met
    by developing a positive and trusting relationship with
    the person being cared for as well as their family/carers
    [10]. Therefore, the discrete elements of fundamental
    care can be described as: actions to meet patients’ physical needs, and their psychosocial (wellbeing and mental
    health) needs; these actions include nurses’ transactional
    and relational behaviours [9].
    The combination of SARS-CoV-2 symptoms and infectiousness of the SARS-CoV-2 virus may pose significant challenges for meeting patients’ physical and
    psychosocial needs, as well as impacting on nurses’ relational and transactional care behaviours. Such challenges
    may result in ‘missed care’ or ‘care left undone’, defined
    as any aspect of nursing care that is omitted or delayed,
    in part or in whole [11, 12]. Whilst our current study focuses specifically on fundamental nursing care, missed
    care can therefore include areas of fundamental nursing
    care (e.g. meeting patients’ hygiene needs) as well as
    other areas of nursing care (e.g. discharge planning) [13].
    Prior to the SARS-CoV-2 pandemic, both nurses and patients indicated that important elements of fundamental
    nursing care are regularly missed, including nutrition,
    hygiene (e.g. bathing; mouth care), ambulation/ supporting
    mobility, communication/ talking with patients, and
    emotional and psychological support [13–17]. The extent
    of missed care is related to poor patient outcomes,
    increased mortality and adverse events, and poor patient
    satisfaction and experience of care [15, 18–20]. Factors contributing to missed care include high patient to registered
    nurse ratios, associated lack of nurse time, patient dependency/ acuity, and the practice environment (e.g. managerial
    support) [12, 16, 17, 21], and the likely impact of the SARSCoV-2 pandemic on all of these factors may further increase incidences of missed care. Indeed, we know from
    nurses’ narrative accounts of the Canadian SARS outbreak
    in 2003 that Personal Protective Equipment (PPE) [22],
    time pressures [23] and visitor restrictions [24] can lead to
    patients feeling abandoned by nurses [23].
    Given the short time since the SARS-CoV-2 virus first
    emerged in late 2019, knowledge of its impact on nursing care has been slow to emerge and as yet there is no
    direct data on patients’ experience of nursing care. Most
    of the research published to date has focussed on the
    impact on nurses’ wellbeing, not on their processes of
    caring. Thus, we know from surveys conducted in China
    and Italy that front-line nurses have experienced huge
    workload; long-term fatigue; infection threat; and anxieties and frustration concerning the death of patients for
    whom they cared. Additionally, they worried about their
    families and vice versa [25]. A survey completed by 764
    nurses (60.8%) and 493 physicians (39.2%) from 34 hospitals in China reported symptoms of depression (634
    [50.4%]), anxiety (560 [44.6%]), insomnia (427 [34.0%]),
    and distress (899 [71.5%]) amongst the health care
    workers. Nurses, frontline health care workers, female
    health care workers, and those working in Wuhan, reported more severe mental health symptoms than other
    health care workers [26]. Nurses in Italy reported PostTraumatic Stress Disorder symptoms, severe depression,
    anxiety, insomnia and perceived stress [27], and UK
    nurses were concerned about the risks of SARS-CoV-2
    on their physical and mental health, as well as the health
    of their families [28, 29].
    Sugg et al. BMC Nursing
    (2021) 20:215
    There is evidence emerging from the UK that these
    effects on nurses, together with the rapid adjustment of
    healthcare systems to accommodate the pressures of increased patient flow, redeployment of inexperienced staff
    into isolation care environments, and other factors, may
    have had a negative impact on patients. One survey on
    recovered patients’ experiences at discharge found that
    82% of respondents had not received post-discharge assessment visits, and 18% reported having unmet needs
    [30]. Thus, the negative impact of the SARS-CoV-2 outbreak on nurses may in turn impact patients, acting as a
    mediator of missed care. However, we do not currently
    know if the concerns raised in the brief reports from the
    Canadian SARS outbreak have been replicated or learnt
    from in this current pandemic, and there are currently
    no evidence-based guidelines for nursing patients with
    SARS-CoV-2 who may be receiving ventilatory support
    without tracheal intubation (i.e. not invasively ventilated), who represent the majority of hospitalised patients with this condition. This leaves nurses without
    guidance and is potentially associated with variations in
    patient experience, care quality and costs as redeployed
    and/or inexperienced nurses struggle to adapt to
    caring for patients in strict isolation [31] using unfamiliar
    care procedures required for infection prevention and
    control [32].
    We designed the COVID-NURSE cluster randomised
    controlled trial [33] to evaluate a fundamental nursing
    care protocol for patients hospitalised with the SARSCoV-2 virus not invasively ventilated. The fundamental
    nursing care protocol has been developed from three
    main areas of activity: i) a survey of registered nurses’
    and non-registered auxiliary nursing/ healthcare support
    workers and assistants’ views and experiences of caring
    for patients with SARS-CoV-2 including the barriers encountered in delivering fundamental care and strategies
    adopted to overcome these; ii) a rapid systematic review
    of the literature [34]; and iii) four co-creation workshops
    involving nurses and patients with experience of being
    hospitalised with the SARS-CoV-2 virus not invasively
    ventilated, in which the findings from the survey and the
    systematic review were presented and discussed.
    In this paper, we report the findings from the survey
    of nurses that relate to their views and experiences of
    missed fundamental care and barriers to fundamental
    care for inpatients with SARS-CoV-2 not invasively ventilated. We will report findings on strategies used to
    overcome the barriers to care in a future article, to avoid
    potential contamination of the trial before completion.
    Methods
    Aim and design
    Our aim was to identify the views and experiences of
    registered nurses and non-registered nursing care staff
    Page 3 of 17
    on missed fundamental care and the barriers to fundamental care for inpatients with the SARS-CoV-2 virus
    not invasively ventilated. We conducted a cross-sectional
    study employing a mixed methods explanatory design
    [35] guided by a pragmatic philosophy [36]. For the
    quantitative and qualitative components, we collected
    data concurrently and analysed data sequentially (with
    qualitative data analysed in order to explain the quantitative data). We gave the quantitative component greater
    priority as this guided our analysis of qualitative data,
    and we mixed the components during data analysis. This
    approach enabled us to utilise the qualitative data to
    elaborate on, clarify, illustrate and contextualise the key
    quantitative findings [37, 38].
    Participants and recruitment
    Eligible respondents were UK-based registered nurses
    and non-registered auxiliary nursing/ healthcare support
    workers/ assistants that had actively engaged in nursing
    inpatients with the SARS-CoV-2 virus who were not invasively ventilated. Thus, respondents who had nursed
    patients who were not ventilated, or patients who received non-invasive ventilation, were eligible; respondents who only nursed invasively ventilated patients
    were ineligible. We invited a convenience sample of
    respondents using a range of strategies; including a database of nurses who had consented to be approached for
    SARS-CoV-2 related research studies through their involvement in the ‘Impact of COVID-19 on the Nursing
    and midwifery workforce’ (ICON) study [29]; networks
    of senior research, management and clinical nurses in
    England and Wales including contacts within the
    National Institute for Health Research (NIHR) 70@70
    research network, the Association of UK Lead Research
    Nurses, the Royal Colleges, and hospital sites affiliated
    with the COVID-NURSE Trial co-investigators; the UK
    NIHR Clinical Research Network; and through social
    media including Twitter and University of Exeter channels. We aimed for our survey distribution channels to
    be as inclusive as possible in terms of encouraging
    responses from nurses working in different types of
    hospitals, including general vs. specialist, which were
    geographically diverse and serving populations of different ethnicities.
    We sent a link to the survey to nurses on our database
    and to key gatekeepers in the networks listed above. We
    asked gatekeepers to circulate the link via newsletters,
    emails and other communication channels appropriate
    to their networks with a covering letter informing potential respondents of the purpose and timeframe for the
    survey. The landing page for the survey provided links
    to the participant information sheet, frequently asked
    questions, and the survey. As this was an exploratory
    study to guide our intervention development, within the
    Sugg et al. BMC Nursing
    (2021) 20:215
    specific time limits of the COVID-NURSE trial and thus
    using a convenience sampling frame, we did not have a
    predetermined sample size calculation and sought to
    recruit as many respondents as possible during the timeframe of the survey.
    Data collection and materials
    The survey was open for 3 weeks, plus 3 days to respondents who had commenced the survey, to provide the opportunity to complete it. We developed the survey with
    input from the COVID-NURSE trial Co-Investigators and
    members of the wider research team, in response to formal and informal feedback from four nursing teams who
    piloted the survey, and in line with comments from the
    University of Exeter Medical School Ethics Committee. At
    all times in the development of the survey we involved
    members of our patient and public involvement group
    (PPI) including our PPI co-investigators and trial management group member, who gave us advice on the survey
    design. Using Qualtrics™ online survey software [39], we
    designed a bespoke online series of survey questions
    including demographic items. We structured our survey
    according to the Fundamentals of Care model [8, 9]. We
    included three sections on physical, relational and psychosocial areas of care, and subsections in each of these areas
    corresponding to sub-categories of care as adapted from
    Feo et al. (2018) [9] (Table 1).
    In each subsection (Table 1), we asked respondents to:
     Rate how well they thought they were able to meet
    Page 4 of 17
    (excluding those who had been invasively ventilated)
    compared to their ability to meet the needs of other
    patients they were experienced in nursing before
    SARS-CoV-2. For example, for section one (physical
    care), subsection one, respondents were asked to
    rate how well they were able to meet the hygiene,
    personal cleansing and toileting needs of patients
    with the SARS-CoV-2 virus (excluding those who
    had been invasively ventilated) compared to their
    ability to meet the hygiene, personal cleansing and
    toileting needs of other patients they were
    experienced in nursing before SARS-CoV-2.
    Respondents were asked to provide answers on a five
    point Likert-type scale with the following options:
    much better than, a little bit better than, the same
    as, a bit worse than, or much worse than.
    Alternatively, respondents could indicate that they
    were not involved in this area of care;
     Provide free text to narratively identify and describe
    examples of missed fundamental care;
     Select all relevant barriers to fundamental care from
    a list provided. The barrier list was derived from
    discussions with the COVID-NURSE trial CoInvestigators with expertise in nursing. Barriers were
    standardised across all sub-categories, with
    additional barriers added where relevant for a
    specific category. A list of barriers available for each
    sub-category is provided in Additional file 1;
     Provide free text to narratively identify and describe
    examples of barriers to fundamental care.
    the needs of patients with the SARS-CoV-2 virus
    Data analysis
    Table 1 Survey structure; fundamental care areas and subcategories of care
    Section: Care area
    Subsection: Sub-category of care
    1. Physical
    1. Hygiene, personal cleansing and toileting
    2. Eating and drinking
    3. Rest and sleep
    4. Mobility
    5. Patient comfort
    6. Patient safety
    7. Medication management
    2. Relational
    1. Establishing a relationship with patients
    2. Talking and listening
    3. Non-verbal communication
    4. Shared decision-making
    5. Communicating with relatives, carers and
    significant others
    3. Psychosocial
    1. Dignity and respect
    2. Respecting patients’ values and beliefs
    3. Wellbeing, anxiety and depression
    The UK Clinical Research Collaboration (UKCRC)-registered University of Exeter Clinical Trials Unit received,
    cleaned and processed the data, and uploaded datasets
    to Microsoft Excel [40]. We applied pairwise deletion to
    each survey item in order to maximise the data available,
    and reported all percentages as the percentage of the
    total number of respondents who provided data for that
    survey item. We combined ethnicity data into standard
    categories [41].
    Quantitative data analysis
    We analysed quantitative data, including demographic
    data, descriptively. For respondents’ ratings of care, we
    combined responses into four categories for ease of interpretation: 1) better than other patients (combining
    ‘much better’ and ‘a little bit better’); 2) the same as
    other patients; 3) worse than other patients (combining
    ‘much worse’ and ‘a bit worse’); 4) not involved in this
    area of care. For both ratings of care and barriers to
    care, we calculated the frequency, and percentage, of respondents selecting each option for each sub-category of
    care. We also calculated the percentage of respondents
    Sugg et al. BMC Nursing
    (2021) 20:215
    selecting each barrier in total across each of the three
    care areas (physical; relational; psychosocial).
    Qualitative and mixed methods data analysis
    We achieved familiarisation with the data through reading
    survey responses and analysed data using Framework
    Analysis [42] to allow for both inductive and deductive approaches in combining our study aims/ survey questions
    with participants’ original accounts [42, 43]. In undertaking qualitative analysis within our explanatory mixed
    methods design, we focused on explaining the key quantitative findings rather than completing a full, independent
    analysis of qualitative themes, so that we could understand
    respondents’ meanings in providing their quantitative
    responses and focus in on qualitative examples in key
    problem areas indicated by the quantitative data.
    Data interpretation and the development of analytic
    categories were discussed by a multidisciplinary team
    trained in qualitative data analysis and consisting of five
    researchers (HVRS, A-MR, HI-S, DAR, NM) with backgrounds in nursing (3), nursing education (3), mental
    health services research (2) and clinical research (2). The
    team was led by HVRS; A-MR, HI-S, NM and HVRS independently coded subsets of the raw data; HVRS
    double-coded and verified subsets of the data coded by
    A-MR, HI-S and NM.
    For missed care and barriers, we separately coded
    responses into a framework structured according to the
    Fundamentals of Care Framework. Within each subcategory of care, we analysed survey responses thematically
    using a constant comparison approach, and examined similarities and differences in respondents’ accounts in order to
    categorise the examples of missed care and barriers for each
    sub-category [44, 45]. For barriers to care, we then focused
    our analysis on the main barriers highlighted by the quantitative data, categorising the qualitative findings across all
    sub-categories of care into each of the top five rated barriers for each of the three care areas (physical; relational;
    psychosocial). We have integrated the quantitative and
    qualitative data in side-by-side comparison tables [35] organised by the quantitative data (for missed care, from highest
    to lowest percentage of respondents rating the sub-category
    of care as ‘worse’; for barriers to care, from highest to lowest percentage of respondents selecting the barrier). In
    these tables we have included summaries of the qualitative
    findings and quotes to illuminate these.
    We describe our study in line with cross-sectional
    study reporting guidelines (see Additional file 2 for completed STROBE checklist) [46].
    Results
    Respondent characteristics
    From 3rd to 26th August 2020, 1062 eligible respondents consented to provide survey data; 84 of these
    Page 5 of 17
    provided no further data. The number of respondents
    providing data for each survey item is provided in
    Additional file 1. Respondent characteristics are summarised in Table 2.
    Respondents’ views on missed fundamental care
    Quantitative results
    The percentage of respondents rating the physical,
    relational and psychosocial care of patients with the
    SARS-CoV-2 as worse, the same as, or better than other
    patients, for each constituent sub-category of care, is
    shown in Figs. 1, 2 and 3. Frequencies are provided in
    Additional file 1.
    For sub-categories of care across all three care areas
    (physical, relational, psychosocial), a majority of
    respondents rated their ability to meet the needs of
    SARS-CoV-2 patients as worse than for other patients.
    The following sub-categories were rated as worse by a
    majority of respondents: ‘talking and listening’ (57%);
    ‘communicating with relatives, carers and significant
    others’ (57%); ‘mobility’ (56%); ‘non-verbal communication’ (54%); ‘emotional wellbeing, anxiety and depression’
    (53%). Just less than half (49%) of respondents also rated
    ‘establishing a relationship with patients’ as worse for
    SARS-CoV-2 patients. For all the other physical subcategories (aside from ‘mobility’), approximately one
    third or less of respondents rated care as worse for
    SARS-CoV-2 patients (range 26–34%). For relational
    care, almost one third of respondents (32%) rated
    ‘shared decision-making’ as worse for SARS-CoV-2 patients, and for psychosocial care ‘dignity and respect’ and
    ‘respecting patients’ values and beliefs’ were rated as
    worse for SARS-CoV-2 patients by 26 and 19% of respondents respectively.
    Integrated quantitative and qualitative results
    In Tables 3, 4 and 5 we have presented side-by-side
    comparison tables integrating the quantitative findings
    and summarised qualitative findings on missed care for
    each sub-category of physical, relational and psychosocial care. Respondents’ ID numbers are included in
    brackets after quotes.
    Between 26 and 56% of respondents struggled to
    meet all sub-categories of patients’ physical needs efficiently and effectively compared to patients they would
    normally care for. Particularly highlighted were restrictions on patients’ mobilisation outside of side (isolation)
    rooms, and some respondents also described issues with
    interrupted sleep; missed and delayed personal care, particularly mouth care; restrictions and delays in providing
    food and drink; reductions in observing patients in side
    rooms; errors and potential for errors, particularly
    around medications; challenges with controlling symptoms of breathlessness and high temperature; missed
    Sugg et al. BMC Nursing
    (2021) 20:215
    Page 6 of 17
    Table 2 Respondent characteristics
    Table 2 Respondent characteristics (Continued)
    N (%)
    Gender
    Age
    Ethnicity
    Environment
    Country
    Main position
    Redeployed?
    Female
    858 (87.7)
    Male
    112 (11.5)
    Prefer not to say
    8 (0.8)
    < 25 98 (10.0) 26–30 173 (17.7) 31–40 257 (26.3) 41–50 234 (23.9) 51–60 182 (18.6) 61–66 26 (2.7) > 67
    1 (0.1)
    Prefer not to say
    7 (0.7)
    Asian/ Asian British
    32 (3.3)
    Black/ African/ Caribbean/
    Black British
    15 (1.5)
    Mixed/ Multiple ethnic groups
    13 (1.3)
    Other ethnic group
    46 (4.7)
    Other White
    85 (8.7)
    White British
    779 (79.7)
    Prefer not to say
    8 (0.8)
    Acute General NHS hospital
    including teaching hospital
    898 (91.8)
    Tertiary/ specialist
    63 (6.4)
    Private healthcare
    6 (0.6)
    Missing data
    11 (1.1)
    England
    933 (95.4)
    Wales
    15 (1.5)
    Scotland
    5 (0.5)
    Northern Ireland
    4 (0.4)
    Other country
    1 (0.1)
    Missing data
    20 (2.0)
    Charge nurse
    206 (21.1)
    Staff nurse
    374 (38.2)
    Specialist/ advanced nurse
    142 (14.5)
    Research nurse
    42 (4.3)
    Nurse researcher
    1 (0.1)
    Manager
    73 (7.5)
    Student nurse
    20 (2.0)
    Non-registered nursing
    associate
    10 (1.0)
    Non-registered care
    or nursing assistant
    90 (9.2)
    Missing data
    20 (2.0)
    Yes
    139 (14.2)
    No
    227 (23.2)
    Missing data
    612 (62.6)
    N (%)
    Usually work on
    respiratory warda?
    Usually work in
    non-warda environment?
    Yes
    114 (11.7)
    No
    252 (25.8)
    Missing data
    612 (62.6)
    Yes
    138 (14.1)
    No
    228 (23.3)
    Missing data
    612 (62.6)
    a
    Ward: an inpatient division in a hospital typically shared by patients who
    need a similar type of care. Non-ward: a non-residential health care setting
    such as outpatient, community or primary care. Percentages may not always
    total 100 due to rounding
    pressure area care; and a lack of presence from multidisciplinary colleagues such as physiotherapists, dieticians
    and pharmacists.
    In relational care, the majority of respondents (57%)
    highlighted communication difficulties with patients and
    their significant others, with almost half of respondents
    reporting that this impacted on their ability to establish
    a relationship with patients. Respondents struggled to
    build rapport with patients; experienced restrictions in
    being heard, understood, and spending time with patients; and were less able to use facial expressions, nonverbal cues and touch to comfort patients. Respondents
    reported that patients missed having visits from significant others, and they struggled to both keep significant
    others informed and obtain information about patients
    from them. A third of respondents also experienced
    shared decision-making as more rushed and policy-led
    than usual.
    In psychosocial care, the majority of respondents
    (53%) reported struggling to support patients’ emotional
    wellbeing and mental health, typically prioritising
    functional and physical care over emotional care. Most
    respondents were unable to provide usual levels of
    support, reassurance and interaction with patients, and
    reported that patients experienced isolation, loneliness,
    fear and low mood. A minority of respondents also had
    difficulties maintaining patients’ privacy and dignity,
    such as drawing curtains for personal care or distressing
    scenes; lacked knowledge about patients’ beliefs; and
    noted a lack of presence from psychological services and
    chaplaincy.
    Respondents’ views on barriers to fundamental care
    Quantitative results
    We summarise the percentage of respondents selecting
    each barrier in Table 6 (presented as the average percentage of respondents selecting the barrier, and the
    range of respondent percentages, across the constituent
    sub-categories of physical, relational and psychosocial
    care; where the barrier was only an option for one subcategory, we just present the percentage of respondents
    Sugg et al. BMC Nursing
    (2021) 20:215
    Page 7 of 17
    Fig. 1 Respondents’ ratings of meeting the physical care needs of patients with SARS-CoV-2
    selecting the barrier for that sub-category). We have
    listed barriers in the order of most to least frequently selected across all care areas. We have provided the number of respondents selecting each barrier for each subcategory of care in Additional file 1.
    In total, eight barriers were ranked within the top five
    in at least one of the three care areas (Tables 7, 8 and 9).
    ‘Wearing PPE’, and the ‘severity of the patient’s condition’ were the most frequently selected barriers and were
    among the top five barriers to all three care areas. The
    third most frequently selected barrier, ‘difficulties taking
    items/ equipment in and out of isolation rooms’, was
    among the top five barriers to physical care. ‘Lack of
    time’, the fourth most frequently selected barrier, was
    among the top five barriers to both psychosocial and relational care. ‘Lack of personnel, skill mix, catering,
    housekeeping or dietetic support’, the fifth most frequently selected barrier, was among the top five barriers
    to both physical and psychosocial care. The sixth most
    frequently selected barrier, ‘lack of knowledge about
    COVID-19’, was among the top five barriers to both relational and psychosocial care. The seventh most frequently selected barrier, ‘not enough physical resources
    such as equipment/ washing facilities/ stock items’, was
    the final top five barrier to physical care. The eighth
    most frequently selected barrier, ‘fear of catching
    COVID-19’, was the final top five barrier to relational
    care.
    Integrated quantitative and qualitative results
    In Tables 7, 8 and 9 we report the top five barriers per
    care area in order of highest to lowest percentage of respondents selecting this barrier across the constituent
    sub-categories. We also include the sub-category for
    which the highest percentage of respondents selected
    the barrier in that care area, and then integrate the
    qualitative data in side-by-side comparison tables. Respondents’ ID numbers are included in brackets after
    quotes.
    Respondents struggled to meet the physical care needs
    (particularly rest and sleep, mobility, eating/drinking,
    and personal care) of patients who were very unwell,
    often attached to oxygen equipment, and with high
    monitoring requirements. Wearing PPE also created a
    physical barrier to meeting such needs, particularly hygiene needs. A lack of storage and stock supplies in
    Sugg et al. BMC Nursing
    (2021) 20:215
    Fig. 2 Respondents’ ratings of meeting the relational care needs of patients with SARS-CoV-2
    Fig. 3 Respondents’ ratings of meeting the psychosocial care needs of patients with SARS-CoV-2
    Page 8 of 17
    Sugg et al. BMC Nursing
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    Page 9 of 17
    Table 3 Side-by-side comparison of quantitative and qualitative data on missed physical care
    Care category (%
    rating care as
    worse)
    Summary of qualitative data on missed care
    Quotes demonstrating qualitative data
    Mobility (56%)
    Patients in side roomsa were unable to mobilise by moving freely
    on the ward and walking to the toilet. Patients were also unable
    to access facilities such as the gym or garden, or complete stair
    assessments. Pressure area care and rehabilitation could be
    missed, and respondents experienced a lack of physiotherapy
    presence/ support.
    “Due to needing to isolate … one of our patients was in
    his room for 4 weeks.” (ID581)
    “Physios would leave C19+ patients to be seen at the end
    of the day, resulting in a shortened session or missed
    session.” (ID244)
    Rest and sleep (34%) Patients often experienced sleep which was interrupted by
    consistent monitoring/ observations and interventions, and by
    noise and lights. Patients also experienced a lack of time for
    sleep, difficulties settling, and poor quality sleep.
    “There was not much “down time” during the night.”
    (ID585)
    “It was so busy that we couldn’t even switch off the lights
    … sleep deprivation was present on every night shift.”
    (ID355)
    Patient safety (34%)
    Respondents highlighted a reduction in monitoring/ observing
    patients who were in closed bays or side rooms, and a related
    increased risk of falls. Respondents also noted various errors and
    potential for errors, such as medication errors and failures to
    escalate, and that regular skin checks could be missed.
    “Need to isolate patients into side rooms was treated
    (rightly or wrongly) as more important than their risk of
    falls.” (ID286)
    “Medication rounds not done next to patient. Nursing staff
    not present in the bays so often.” (ID512)
    Eating and drinking
    (33%)
    Respondents noted issues with food/drink supplies such as
    running out of drinks, lack of choice for patients, and difficulties
    for patients eating using plastic plates/cutlery. There were some
    delays in providing food and drink to patients, and between
    meals these needs could be missed. Some patients were
    weighed less regularly and some respondents experienced less
    presence from dieticians.
    “Poor nutritional intake for those most vulnerable. Missed
    regular cups of tea … Gut-wrenching as a nurse.” (ID20)
    “Tea trolleys and meal choices were much harder to
    facilitate. It took longer for diet and fluid to get to
    patients.” (ID262
    Patient comfort
    (32%)
    Symptom control was challenging, particularly breathlessness and
    temperature, and oxygen equipment was uncomfortable. Patients
    missed having visitors, and interaction/ time with nurses, which
    affected their comfort levels. Respondents also noted that nursing
    patients in the prone position (‘proning’) and difficulties turning
    patients meant pressure area care could suffer.
    “Patients were uncomfortable due to nature of condition,
    positioning (extended time prone giving them sore joints
    or back).” (ID475)
    “Unable to comfort emotionally distressed patients due to
    PPE. Lack of family support.” (ID464)
    Hygiene, personal
    cleansing and
    toileting (27%)
    Patients’ personal care could be missed or delayed, particularly
    mouth care, but also washes, hair brushing and toileting. Less
    time was spent on personal hygiene, with some patients
    expected to meet these needs themselves yet not encouraged to
    do so. Patients’ rooms were also cleaned less often, and patients
    often couldn’t access private bathrooms.
    “Delayed response to washes, often flowing into
    afternoon.
    Personal care, oral care, often missed completely.” (ID20)
    “Less assistance. Patient left or expected to meet most
    hygiene needs themselves and not pushed or encouraged
    to do this.” (ID130)
    Medication
    management (26%)
    Some staff were unable to double check medications and some
    reported an increase in medication errors. There could be delays
    in receiving and administering medications, and some
    respondents ran out of medications. Respondents also
    experienced a lack of pharmacist presence/support.
    “I made my first medication error during the pandemic…
    Thankfully no one was hurt, but it still haunts me.” (ID529)
    “Medications were not available … Pharmacists refused to
    come to the wards.” (ID703)
    a
    Side rooms: rooms in which individual patients stay in isolation from other patients
    SARS-CoV-2 areas, and the increased need to clean
    items between uses, meant insufficient supplies for respondents to meet patients’ needs and make them comfortable. The need to don and doff PPE upon entering
    and leaving a patient’s room delayed responding to patients’ needs, meant staff had to try to prepare all items
    needed in the room before entering, and created difficulties providing patients with items such as food and
    drinks. Respondents also experienced staff shortages and
    a lack of presence from specialised services which increased their own workloads, and compromised patients’
    care and safety.
    Wearing PPE created a very significant barrier to relational care and communicating with patients, compromising hearing, lip reading, seeing facial expressions, use
    of non-verbal cues and touch. PPE also made staff difficult to recognise. Due to staff shortages and high patient
    acuity, respondents had little time to spend talking and
    listening to patients, prioritising a functional approach
    to care. This was compounded by respondents’ reluctance to spend time in patients’ rooms due to fear of
    catching SARS-CoV-2, which limited their ability to establish a relationship with patients. Patients’ ability to
    communicate and participate in decision-making was
    also compromised by the severity of their own conditions, and respondents felt they lacked the knowledge of
    SARS-CoV-2 required to answer patients’ questions during the decision-making process in particular. Running
    through these accounts was the impact of restrictions on
    visitors, for both patients’ wellbeing and staff’s ability to
    Sugg et al. BMC Nursing
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    Page 10 of 17
    Table 4 Side-by-side comparison of quantitative and qualitative data on missed relational care
    Care category (% rating Summary of qualitative data on missed care
    care as worse)
    Quotes demonstrating qualitative data
    Talking and listening
    (57%)
    Many respondents highlighted a lack of rapport building
    with patients, and lack of clear communication with
    patients (i.e. being heard and understood), specifically
    noting the inability to lip read through PPE. Related to this,
    respondents stressed reductions in nurse-patient contact,
    including both physical touch and time spent with patients.
    “Wearing PPE especially masks meant that patients often
    could not hear you and you would have to repeatedly talk
    to them which made conversation and flow more difficult.”
    (ID328)
    “You can’t hear properly with shields. You can’t see
    properly. I lip read as well as listen, this is very difficult.
    Verbal [communication] is difficult with softly spoken
    patients.” (ID505)
    Communicating with
    relatives, carers and
    significant others (57%)
    Patients missed having visits from significant others and
    were accordingly isolated. Staff had less opportunity to
    build relationships with significant others and manage their
    emotional needs, and noted that significant others were
    not always updated in a timely and regular manner. Staff
    experienced difficulties keeping significant others fully
    informed over the phone whilst ensuring confidentiality
    was maintained.
    “Patients struggled with lack of family contact.” (ID573)
    “Regular updates with relatives and carers were not always
    achieved.” (ID427)
    “It has also been difficult building a rapport with families
    and relatives… This has added difficulty as they are unable
    to see the environment their loved one is being care in.”
    (ID579)
    Non-verbal
    communication (54%)
    Staff were less able to communicate with patients using
    facial expressions, non-verbal cues, physical gestures and
    touch. Some respondents therefore felt that they were
    showing less comfort, reassurance, empathy and friendliness towards patients. They also had a reduced ability to
    pick up on patients’ non-verbal cues and respond to their
    needs accordingly.
    “Patients unable to read facial expressions, see non-verbal
    cues, see the nurse was being empathetic and compassionate to their needs as they were unable to see nurse’s faces.”
    (ID332)
    “Visitors (who normally pick up on missed cues) unable to
    visit.” (ID204)
    Establishing a relationship Some respondents highlighted the same issues as
    with patients (49%)
    experienced in relation to ‘talking and listening’, also noting
    that it was harder to get to know these patients; that
    functional care could be prioritised over relationship
    building; and that they missed opportunities to obtain
    information about patients from their significant others as
    usual.
    “The human aspect of nursing care. Not being able to
    smile. To sit and make a cup of tea and listen to the
    patient’s opinion of how their stay was going. Every aspect
    of nursing became clinical.” (ID20)
    “Difficult to hear and communicate whilst wearing PPE,
    therefore loss of personal touch.” (ID585)
    Shared decision-making
    (32%)
    “Due to nature of virus decisions were often made in
    patients’ best interests, without being able to discuss them
    with patient or family.” (ID204)
    “It was decided that all patients over a certain age would
    be DNAR, it was hard to justify this.” (ID368)
    Some respondents experienced decision-making as more
    rushed and policy-led (e.g. escalation/ resuscitation plans)
    with somewhat less involvement from the patient and significant others. Staff were also less equipped than normal
    with the knowledge required to answer patients’ questions
    and provide information during decision-making.
    DNAR Do Not Attempt Resuscitation
    Table 5 Side-by-side comparison of quantitative and qualitative data on missed psychosocial care
    Care category (%
    rating care as
    worse)
    Summary of qualitative data on missed care
    Quotes demonstrating qualitative data
    Emotional wellbeing,
    anxiety and
    depression (53%)
    Respondents noted that patients’ physical care was prioritised over
    their emotional needs. Staff were unable to provide normal levels
    of support e.g. skin to skin touch; time for communication and
    listening. Patients experienced isolation; and little interaction with
    staff, significant others, or other patients. Respondents observed
    fear and low mood across patients, and were unable to reassure
    patients with knowledge about the virus/ treatments. Respondents
    also noted a lack of presence/support from psychological services.
    “Some days it was just task orientated and we just needed to get
    to the end of the shift without anyone dying.” (ID593)
    “We weren’t able to even give a patient a hand to hold that didn’t
    have a glove on it and a face covered in a mask.” (ID354)
    “Unable to refer patients to psychology for support or to have
    relatives to visit or for patients to go outside.” (ID196)
    Dignity and respect
    (26%)
    Some respondents reported experiencing difficulties maintaining
    privacy and dignity for patients, such as closing curtains when
    performing personal care. Patients who would normally use the
    bathroom had to use the commode, and patients had to wear
    hospital gowns rather than their own clothes. Proning patients
    was also considered undignified, and some respondents
    experienced patients dying in bays with no privacy.
    “A lack of space, and having often 2 patients in one bedspace
    meant that privacy was difficult. We had access to some privacy
    screens, but nowhere near enough.” (ID377)
    “Proning can be undignified due to the nature of the positioning
    and amount of people it requires to undertake.” (ID585)
    “Patients dying next to them was very distressing.” (ID298)
    Respecting patients’
    values and beliefs
    (19%)
    Some respondents noted a lack of knowledge of patients’ beliefs
    as patients were unable to inform them and/or significant others
    were not present to guide them. Respondents experienced a lack
    of chaplaincy support on the wards. Patients were also unable to
    leave their rooms to visit the prayer room/ chapel, and could not
    access family/community support as they normally would.
    “We didn’t have chaplaincy visiting. We weren’t able to spend
    time with our dying patients in the same way. We didn’t always
    know the patient’s spiritual or religious beliefs. We often didn’t
    know much at all about them.” (ID354)
    “Patients from certain cultures were unable to behave in the usual
    way due to restrictions.” (ID487)
    Sugg et al. BMC Nursing
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    Table 6 Percentage of respondents selecting each barrier to care (average and range across sub-categories)
    Barrier
    Physical Care
    Relational Care
    Psychosocial care
    Wearing PPE
    33% (21–44%)
    61% (37–77%)
    44% (36–48%)
    Severity of the patient’s condition
    41% (33–50%)
    29% (21–47%)
    37% (35–39%)
    Difficulties taking items / equipment in and out of isolation rooms for
    patients nursed in these environments
    38% (28–54%)
    13% (9–18%)
    17% (13–21%)
    Lack of time
    22% (12–29%)
    31% (24–41%)
    37% (30–40%)
    Lack of personnel, skill mix, catering, housekeeping or dietetic support
    30% (11–38%)
    12% (9–17%)
    24% (20–27%)
    Lack of knowledge about COVID-19
    23% (13–34%)
    16% (8–28%)
    25% (18–30%)
    Not enough physical resources such as equipment/washing facilities/
    stock items e.g. water jugs, disposable cups, patients’ teeth
    24% (12–28%)
    12% (4–34%)
    14% (10–19%)
    Fear of catching COVID-19
    21% (13–30%)
    19% (11–25%)
    23% (22–24%)
    Frequent changes in hospital, Trust or organizational policies
    22% (15–35%)
    12% (7–20%)
    15% (14–15%)
    Lack of appropriate PPE
    17% (11–26%)
    8% (5–11%)
    10% (10%)
    Lack of ability to establish a meaningful rapport with the patient
    9% (5–17%)
    15% (12–22%)
    14% (11–19%)
    Lack of information about the ward or patient
    10% (6–14%)
    9% (7–11%)
    16% (12–24%)
    Competing requirements of essential medical interventions
    15% (13–20%)
    9% (4–11%)
    11% (10–13%)
    Lack of ability to regulate the environment (noise level, lighting,
    remote monitoring)
    42% (34–49%)
    N/A
    N/A
    Lack of relevant personal expertise
    11% (6–16%)
    7% (4–11%)
    11% (9–12%)
    Lack of personal psychological support
    7% (5–10%)
    7% (5–10%)
    11% (7–17%)
    Lack of personal emotional capacity
    6% (2–9%)
    7% (5–10%)
    9% (7–14%)
    Lack of access to changing facilities for PPE
    9% (6–17%)
    4% (2–5%)
    5% (4–7%)
    Lack of leadership from senior nurses or managers
    8% (5–13%)
    6% (3–9%)
    8% (7–10%)
    Lack of privacy for the patient
    51%a
    N/A
    N/A
    Inability to meet the patient’s dietary requirements
    13%a
    N/A
    N/A
    Other
    5% (3–7%)
    5% (2–17%)
    7% (6–9%)
    a
    No range provided as barrier only offered as an option for one sub-category of care
    communicate with significant others, particularly in the
    context of a lack of time to update significant others remotely and consult on time critical decision-making.
    Respondents experienced similar barriers to psychosocial care as to relational care, including the impact of
    restrictions on visitors. Patients’ wellbeing and staffs’
    ability to create therapeutic relationships suffered as a
    result of the barriers to communication presented by
    PPE. Again, staff had limited time to spend supporting
    patients’ emotional and spiritual needs; patients’ abilities
    to communicate their needs and beliefs were compromised by the severity of their conditions; and staff found
    it difficult to answer patients’ questions about SARSCoV-2 or provide them with reassurance. The lack of
    SARS-CoV-2 knowledge also caused fear and anxiety for
    patients. Respondents experienced a lack of presence
    from psychology services and chaplaincy which limited
    support for patients, and some lacked the expertise to
    support patients’ psychological needs.
    Discussion
    In this survey, we found that respondents rated their
    ability to meet patients’ needs in many areas of
    fundamental care as worse for hospitalised patients with
    SARS-CoV-2 than for other patients they were experienced in caring for before the pandemic. Although
    meeting patients’ needs was rated by some respondents
    as worse in all areas of care; the majority of respondents
    specifically identified mobility; talking and listening;
    non-verbal communication; communicating with relatives, carers and significant others; and caring for patients’ emotional wellbeing, anxiety and depression as
    poorer. Across the categories of physical, relational and
    psychosocial care, we found the strongest reports of difficulties were with undertaking relational care, with the
    majority of respondents rating their ability to meet patients’ needs as worse in three of the five categories. In
    contrast, although 26–34% of respondents rated elements of physical care as worse, it was only for mobility
    that the majority (56%) cited deficits in this care area
    specifically. For psychosocial care, most respondents
    thought that their ability to meet patients’ needs was at
    least as good or better in the areas of respect, dignity,
    values and beliefs but this contrasts with more than half
    reporting that their ability to address patients’ emotional
    wellbeing, depression and anxiety needs was poorer.
    Sugg et al. BMC Nursing
    (2021) 20:215
    Page 12 of 17
    Table 7 Integration of quantitative and qualitative data on top five barriers to physical care
    Barrier (% selecting
    barrier)
    Highest subcategory (%
    selecting
    barrier)a
    Experiences/ explanations of barriers (from
    qualitative data)
    Quotes demonstrating qualitative data
    Severity of the patient’s
    condition (41%)
    Rest and sleep
    (50%)
    Patients were often fatigued, weak, breathless,
    bedbound, proned, and had high oxygen
    requirements. These factors caused discomfort,
    limited patients’ ability to voice their needs,
    impeded mobility, interfered with eating/drinking,
    and restricted staffs’ ability to provide personal
    care (e.g. bathing; mouth care). The need for
    frequent monitoring also interrupted patients’ rest.
    “CPAP hood made eating and drinking
    opportunities limited … Their rest and sleep was
    broken to perform essential care.” (ID988)
    “The priorities had to change due to maintaining
    organ functions that were in critical states and
    personal care had to be pushed down the priority
    list.” (ID92)
    Difficulties taking items/
    equipment in and out of
    isolation rooms (38%)
    Eating and
    drinking (54%)
    Staff spent extra time cleaning items which had
    entered patients’ rooms, and struggled to prepare
    all items ready to take in to avoid donning and
    doffing PPE. Specific difficulties included providing
    meals/drinks and equipment to support mobility,
    removing plates/trays and waste products, and
    not being able to take drug charts into rooms.
    “There was a big time lag of having to don and
    doff in and out of rooms if you forgot a flush, or
    needed another syringe.” (ID20)
    “The rooms for isolated patients were very small
    and taking equipment in and out and cleaning
    equipment … was very time consuming.” (ID456)
    Wearing PPE (33%)
    Hygiene,
    personal
    cleansing and
    toileting (44%)
    Respondents struggled to meet patients’ physical
    needs, especially personal care and moving/
    turning patients, whilst wearing PPE which was
    hot, difficult to see through, and created a
    physical barrier. Changing PPE between patients
    took time away from meeting their needs, and
    donning PPE delayed responding to patients’
    requests.
    “PPE gear has made delivery of any nursing care
    so much harder, just by the uncomfortable
    wearing of the masks, vision obscured by visas or
    goggles and the heat.” (ID590)
    “Requirement to wear PPE competes with need to
    provide assistance promptly.” (ID286)
    Lack of personnel, skill
    mix, catering,
    housekeeping or dietetic
    support (30%)
    Patient safety
    (38%)
    Respondents noted a lack of physiotherapists,
    dieticians, pharmacists and domestic staff, which
    delayed patient care. Nursing staff shortages were
    stressed, which meant insufficient staff for tasks
    such as mobilising patients and performing
    personal care. Redeployed staff could also lack
    knowledge of equipment, medications and the
    importance of fundamental care.
    “Pharmacists did not visit the ward and they are
    normally there to support and order drugs so it
    was another thing that we had to do” (ID83)
    “We had plenty of redeployed staff but not always
    staff that were able to be hands on as they had
    not been clinical for many many years.” (ID179)
    Not enough physical
    resources such as
    equipment (24%)
    Patient comfort
    (28%)
    Respondents reported shortages of items
    including feed pumps, chairs, hoists, food, hot
    drinks, bottled water, weighing equipment,
    curtains, commodes, soap, wipes, medications and
    PPE. This was related to a lack of storage in
    COVID-19 areas, inability to share items with other
    areas, and need to clean items between uses. This
    impeded patient mobilisation and the timely completion of tasks.
    “Chronic shortage of pretty much everything.”
    (ID80)
    “Simple things like a tray to take food in to
    isolation rooms in short supply” (ID98)
    “Lack of specialist equipment on COVID wards
    (due to storage or lack of enough equipment to
    spread between cohort/non-cohort ward)” (ID4)
    a
    Highest sub-category = sub-category for which the highest percentage of participants selected the barrier
    Respondents identified clear reasons why they
    thought these elements of care were worse for these patients. Foremost was infection control, specifically the
    wearing of PPE and nursing patients in isolation. PPE
    was cited as a barrier to relational care by twice as
    many respondents as any other barrier. It was uncomfortable for respondents, created a barrier to providing
    physical care, and impeded verbal and non-verbal communication. Insufficient stock, and staffs’ inability to
    take items in and out of isolation rooms without donning and doffing PPE, were also significant barriers to
    physical care. These barriers were compounded by the
    severity of the patient’s condition, requiring as it did
    the use of oxygen equipment, proning (nursing patients
    in the prone position), and causing patients’ difficulties
    in communicating when breathless and/or sedated.
    Another top five barrier to physical and psychosocial
    care was the lack of presence from specialist services,
    and a lack of expertise in redeployed staff themselves.
    Time, or the lack of it, prevented respondents from
    talking and listening to patients, although another
    highly cited barrier was staffs’ own reluctance to spend
    time with patients for fear of catching SARS-CoV-2
    themselves. This was compounded by a lack of knowledge
    about SARS-CoV-2 which impeded respondents’ ability to
    answer patients’ questions. Throughout their accounts, respondents noted the impact of restrictions on visitors for
    both patients and nursing staff. This series of barriers conspired to mean that nurses largely focused on the functional, physical aspects of care, with relationship-building
    and addressing patients’ emotional wellbeing becoming a
    secondary priority.
    Sugg et al. BMC Nursing
    (2021) 20:215
    Page 13 of 17
    Table 8 Integration of quantitative and qualitative data on top five barriers to relational care
    Barrier (%
    selecting
    barrier)
    Highest subcategory(% selecting
    barrier)a
    Experiences/ explanations of barriers (from
    qualitative data)
    Quotes demonstrating qualitative data
    Wearing PPE
    (61%)
    Non-verbal
    communication (77%)
    Wearing PPE impeded respondents’ abilities to
    communicate with patients and build a rapport with
    them. It was difficult to hear and be heard and
    understood through PPE; not possible for patients to
    lip read; and not possible for staff to communicate
    using non-verbal cues, facial expressions/ smiles,
    physical gestures or physical touch. PPE also hid
    staffs’ names, made them harder to recognise, and
    caused fear for some patients.
    “The reduction in the human aspect of nursing,
    being wrapped in plastic and shouting at people
    who can’t read your face or mouth was horrible.”
    (ID20)
    “It was so difficult to comfort without touch. It was
    quite alien really.” (ID479)
    “We would be very scary to patients in the
    beginning, as they were not used to staff being in
    full gowns with masks.” (ID39)
    Lack of time
    (31%)
    Communicating with
    Due to staff being off sick, many patients being very
    relatives, carers and
    unwell, and increased workloads, respondents were
    significant others (41%) often too busy to sit with, talk and listen to patients,
    and prioritised a functional approach to care.
    Clustering care, and minimising time spent in
    patients’ rooms, also meant that staff spent less time
    with patients. Respondents also lacked time to
    contact and update patients’ significant others.
    “Due to the pressures of the pandemic on staffing
    and resources sometimes it was hard to spend as
    much time talking to the patients as would be
    desired.” (ID618)
    “Not being able … to sit and make a cup of tea and
    listen to the patient’s opinion of how their stay was
    going. Every aspect of nursing became clinical.”
    (ID20)
    Severity of the Shared decisionpatient’s
    making (47%)
    condition
    (29%)
    Patients were often sedated, using oxygen
    equipment or experiencing delirium, which made it
    difficult for them to communicate, understand their
    care, be involved in decision-making, and contact
    significant others. Visitor restrictions due to the nature of COVID-19 meant that staff could not get to
    know patients through their significant others.
    “Patients were sedated so unable to make
    relationships with them. When they were awake a
    lot experienced delirium.” (ID851)
    “There were many times when patients were not
    well enough and deteriorating so rapidly that we
    did not really have the time to explain every
    available option.” (ID377)
    Fear of
    catching
    COVID-19
    (19%)
    Establishing a
    relationship with
    patients (25%)
    Respondents were reluctant to get physically close
    to patients, and to enter or spend time in their
    rooms, for fear of contracting COVID-19. They were
    often advised to minimise time in the patient’s room.
    Some respondents noted that the quality of PPE did
    not seem adequate, which led to further fear of contracting COVID-19.
    “Peoples’ fear of catching covid meant they rushed
    time with the patient and didn’t engage with them
    as much.” (ID558)
    “Inadequate PPE meant I didn’t want to stay in
    room for longer than necessary therefore I didn’t
    spend extra time getting to know the patient.”
    (ID160)
    Lack of
    knowledge
    about COVID19 (16%)
    Shared decisionmaking (28%)
    Respondents could lack sufficient knowledge of
    COVID-19 to provide patients with reassurance and
    answers about their condition, treatment and likely
    outcomes as much as they usually would. This impeded building a rapport with patients and shared
    decision-making.
    “[It was] challenging to reassure them and build a
    rapport with them, particularly when we couldn’t
    give them much information on the condition or its
    management (due to general limited knowledge).”
    (ID465)
    a
    Highest sub-category = sub-category for which the highest percentage of participants selected the barrier
    Our results support previous work in related areas.
    With previous studies suggesting that fundamental
    nursing care is already regularly missed in the areas
    of mobility, communication and talking with patients,
    and providing emotional and psychological support
    [13–17], our findings highlight the further impact of
    the SARS-CoV-2 virus on meeting patients’ needs in
    these particular areas. Consistent with previous
    explanations for missed care prior to the pandemic
    [12, 16, 17, 21], respondents highlighted patient acuity
    and lack of time as barriers to meeting patients’
    needs, amongst other challenges more specific to the
    pandemic context.
    Respondents’ accounts of the impact of wearing PPE
    on communication and the development of therapeutic
    relationships with patients, and the impact of restrictions
    on visitors for patients’ emotional wellbeing at a time
    when nurses themselves struggled to meet these needs
    due to time pressures and PPE, reflect nurses’ nonempirical accounts of the Canadian SARS outbreak in
    2003 [22–24]. Our findings concur with nurses’ reports
    of high workloads and their fears regarding the risks
    posed by SARS-CoV-2 to themselves [25, 28, 29].
    Respondents’ accounts regarding the impact of these
    factors are consistent with the reports of patients themselves, who may experience poor communication, a lack
    of support and assistance, and insufficient information
    and/or equipment [30]. In addition, relatives, carers and
    significant others can experience poor communication
    from hospital staff and may not be kept well informed
    about the patient [30]. Indeed, our findings regarding
    respondents’ lack of knowledge about SARS-CoV-2 for
    providing patients with information, the barriers they
    report to communication with both patients and their
    significant others, and the lack of supplies reported may
    help to explain such experiences.
    Sugg et al. BMC Nursing
    (2021) 20:215
    Page 14 of 17
    Table 9 Integration of quantitative and qualitative data on top five barriers to psychosocial care
    Barrier (% selecting
    barrier)
    Highest subcategory (%
    selecting
    barrier)a
    Experiences/ explanations of barriers (from
    qualitative data)
    Quotes demonstrating qualitative data
    Wearing PPE (44%)
    Emotional
    wellbeing,
    anxiety and
    depression (48%)
    Wearing PPE limited verbal and non-verbal communication, rapport building, and physical contact
    with patients, which impacted on patients’ wellbeing and staffs’ abilities to develop therapeutic
    relationships and meet patients’ emotional needs.
    Seeing staff in PPE and being unable to recognise
    them caused discomfort.
    “Wearing full PPE impaired the creation of a
    therapeutic relationship with the patient. Both
    patient and staff become de-personalised.”
    (ID443)
    “It must have been terrifying for the patients who
    did wake up seeing us in our full PPE.” (ID80)
    Lack of time (37%)
    Emotional
    wellbeing,
    anxiety and
    depression (40%)
    In the context of visitor restrictions, respondents
    experienced more pressure to provide emotional
    care to patients, but less time to do so as wards
    were so busy. Staff had little time to sit with
    patients, provide support, understand their values
    and beliefs, and attend to their emotional and
    spiritual needs. They were also reluctant to spend
    much time in patient rooms or advised not to.
    “In critical care we are used to providing the
    emotional and psychological support needed, but
    … Covid critical care being busier than usual
    caused a lot of constraints to do this.” (ID229)
    “Lack of time would be the main factor as staff
    couldn’t fully engage with the patient to
    understand their beliefs and wishes.” (ID85)
    Severity of the patient’s
    condition (37%)
    Dignity and
    respect (39%)
    As many patients were sedated, ventilated and/or
    short of breath, staff had little opportunity to
    communicate with them, develop a rapport,
    assess their emotional/spiritual needs, or find out
    their wishes and beliefs. Patients and respondents
    were at times aware when they were likely to die
    which was overwhelming for all involved.
    “The patients were unable to voice their needs.”
    (ID268)
    “Patients’ anxieties were difficult to assess at
    times.” (ID627)
    “Difficult to establish a rapport with patients as
    they were so short of breath/wearing CPAP
    masks, therefore difficult to know what their
    values/ beliefs are.” (ID585)
    Lack of knowledge about Emotional
    COVID-19 (25%)
    wellbeing,
    anxiety and
    depression (30%)
    Due to their lack of knowledge of COVID-19, respondents found it difficult to answer patients’
    questions and reassure them about their care and
    likely outcomes. Patients ‘feared the unknown’
    and had anxiety around the lack of COVID-19
    knowledge. Given a lack of knowledge of how
    COVID-19 may impact on patients psychologically,
    respondents were reacting to this on an ad hoc
    basis.
    “Because it was so new for us too, sometimes it
    was difficult to answer their questions.” (ID13)
    “Lack of knowledge of the disease meant that we
    were unable to reassure patients about their care
    and how they were improving.” (ID161)
    “Patients were very anxious about Covid-19 as so
    much [is] still unknown.” (ID204)
    Lack of personnel, skill
    mix, catering,
    housekeeping or dietetic
    support (24%)
    Due to the COVID-19 risk and some PPE scarcity,
    some respondents reported that psychology reviews were delayed or not undertaken, and chaplaincy/ religious persons were unavailable, even in
    end of life scenarios. General staff also had a lack
    of experience and expertise for identifying and
    supporting patients with psychological problems.
    “As no one could come onto the wards we were
    unable to get a priest or Imam to come and give
    religious support.” (ID37)
    “Lack of experience and expertise in general staff
    for identifying psychological problems and
    helping patients deal with emotional
    consequences of illness.” (ID4)
    Dignity and
    respect (27%)
    a
    Highest sub-category = sub-category for which the highest percentage of participants selected the barrier
    Strengths and limitations
    A key strength of this study is that it is the first to focus
    on fundamental nursing care in the context of SARSCoV-2. Despite the relationship between fundamental
    nursing care, patient experience, treatment outcomes
    and costs, investigation into fundamental nursing care in
    the heavily compromised environment of SARS-CoV-2
    is not an objective of current SARS-CoV-2 research programmes. Prior to this study we lacked knowledge as to
    the specific impact of the SARS-CoV-2 virus on meeting
    patients’ fundamental physical, relational and psychosocial needs.
    A further strength is our use of a mixed methods explanatory design. By collecting and integrating quantitative and qualitative data, we have produced a more
    comprehensive, in-depth and insightful portrait of the
    issues under investigation [35, 36, 47, 48]. To enhance
    the usefulness of our results for informing a future nursing protocol, we have used our qualitative findings to explain, illustrate and contextualise our quantitative
    findings, with a pragmatic focus on understanding the
    key issues which our nursing protocol needs to address
    [36–38]. However, it is possible that full, independent
    thematic analysis of the qualitative data may have
    highlighted different aspects of the data and presented
    the data in a different light.
    A potential limitation of this study is the absence of a
    predefined sample size. We employed a convenience
    sampling frame with a sample size determined by the
    period of time the survey was open for, which was in
    turn constrained by the rapid nature of the wider
    COVID-NURSE trial and the need to gather pandemic
    Sugg et al. BMC Nursing
    (2021) 20:215
    evidence as quickly as possible in a rapidly evolving situation. We also experienced respondent fatigue whereby
    the number of respondents providing data generally reduced as they worked through the survey items [49].
    However, we were not seeking to generalise our findings
    beyond the sampled population via inferential statistical
    methods which would have formed the basis of any sample size calculation [50]. Furthermore, in all qualitative
    items we did reach data saturation, at which point data
    from additional respondents was no longer providing
    additional clarity or insight; thus, our sample size could
    be considered adequate as well as appropriate (as our
    eligibility criteria ensured respondents were experts in
    the area of interest) [51, 52].
    It may have been beneficial to include Allied Health
    Professionals (AHPs) within our sample; however, time
    constraints and timelines for additional ethical approvals
    were prohibitive. The inclusion of AHPs may have provided additional insights, particularly in relation to our
    finding that a lack of presence from AHPs was considered a barrier to fundamental care by respondents. In
    addition, given the proportions of different staff completing the survey, our results largely represent the views
    of registered nurses rather than non-registered members
    of the nursing workforce who may have held differing
    views or offered additional insights.
    Implications and future research
    Whilst our findings concur with non-empirical reports
    from previous pandemics [22–24], to our knowledge this
    study is the first to quantify nurses’ own views as to the
    impact of a highly infectious virus on their work, and to
    combine this with qualitative insights to help explain
    why specific elements of fundamental care are affected.
    As such, it provides clear guidance for educators, clinicians, managers and policy makers on what to expect
    and prepare for in caring for patients in pandemic
    situations.
    Further research should build on these findings, addressing the following remaining questions: what is the
    impact of nurses’ self-reports of missed fundamental
    care on missed fundamental care as experienced by patients?; what are the implications on patient safety issues
    such as reduced mobility, infection, and malnutrition,
    which are often related to missed fundamental care?;
    what strategies can be incorporated in nursing care to
    reduce the frequency and impact of missed fundamental
    care? In our case, we have used these findings together
    with further information from our systematic review,
    and from nurses and patients themselves on strategies to
    confront the barriers to fundamental care identified in
    this study, to devise a guideline and nursing protocol for
    pandemic situations. We are currently testing this protocol in a cluster randomised controlled trial [33].
    Page 15 of 17
    Although our data were collected from a specific nursing context – inpatient care for patients with the SARSCoV-2 virus who were not invasively ventilated – we
    suggest that our results have the potential for generalising to other care environments and other pandemic
    situations globally. Most of the concerns and barriers
    identified by our respondents are not specific to the
    SARS-COV-2 virus, nor their particular nursing environment. Communication is at the heart of all good nursing
    care globally, as it establishes the platform for compassionate and collaborative transactional care which addresses patients’ physical and psychosocial needs [8, 9].
    Intrinsic too is the organisation of care and interprofessional working, as well as nursing education about
    the epidemiology of illnesses and on specific techniques
    to be used. All these areas are not exclusive to the
    current SARS-CoV-2 pandemic and we suggest, therefore, that our results will be useful for others devising
    strategies to support nursing care in other environments
    (such as care homes), other countries and for other
    pandemics.
    Conclusions
    In a survey of nurses caring for patients in hospital with
    the SARS-COV-2 virus not invasively ventilated, the majority of respondents rated their ability to meet the needs
    of these patients as worse than for patients they normally care for in five of 15 specific fundamental care
    areas. These areas included one physical, three relational
    and one psychosocial nursing care area, highlighting that
    communication with patients and their significant others
    was the major and consistent concern for nurses, alongside organising care (especially mobilisation) for patients
    nursed in isolation, and addressing patients’ emotional
    wellbeing and mental health. The major barriers to fundamental care were the wearing of PPE, the severity of
    these patients’ conditions, lack of time, difficulties taking
    items and equipment in and out of isolation rooms, lack
    of interdisciplinary input, lack of knowledge about
    SARS-CoV-2, and fears of catching the illness itself. The
    difficulties faced by nurses in establishing relationships
    with patients led to concerns that care became merely
    functional and not individualised or patient-centred.
    These concerns are unlikely to be specific to the SARSCoV-2 pandemic nor the hospital environments represented by our survey respondents. These results should,
    therefore, be incorporated into subsequent global pandemic planning by nursing leaders.
    Abbreviations
    ARC: Applied Research Collaboration; AHP: Allied Health Professionals;
    COVID-19: Coronavirus disease 2019; CPAP: Continuous Positive Airway
    Pressure; DNAR: Do Not Attempt Resuscitation; ICON: Impact of COVID-19 on
    the Nursing and midwifery workforce; MRC: Medical Research Council;
    NIHR: National Institute of Health Research; NHS: National Health Service;
    PenARC: Applied Research Collaboration South West Peninsula; PPE: Personal
    Sugg et al. BMC Nursing
    (2021) 20:215
    Protective Equipment; PPI: Patient and Public Involvement; RCN: Royal
    College of Nursing; SARS-COV-2: Severe acute respiratory syndrome
    coronavirus 2; STROBE: Strengthening The Reporting of OBservational studies
    in Epidemiology; UKCRC: United Kingdom Clinical Research Collaboration
    Supplementary Information
    The online version contains supplementary material available at https://doi.
    org/10.1186/s12912-021-00746-5.
    Additional file 1. Number of respondents providing data per survey
    item/ selecting each option within each survey item.
    Additional file 2. Completed STROBE 2007 (v4) Statement—Checklist of
    items that should be included in reports of cross-sectional studies.
    Acknowledgements
    We thank the respondents in this study and the other members of the
    COVID-NURSE team for their support: Joanne Cooper; Claire Hulme; Nigel
    Reed; G. J Melendez-Torres; Harry Tripp; Stephen Wootton.
    Authors’ contributions
    DAR designed the study as chief investigator of the COVID-NURSE trial, with
    input from co-investigators HVRS, A-MRu, HI-S, EC, JTC, SC, FD, PL, AMRa, SS,
    MS and ST. A-MRu and DAR designed the survey with input from SB, HH, ST
    and RW; HVRS, DAR and HH obtained ethical and governance approvals with
    support from MK. HVRS, LM and NM completed quantitative data analysis
    with support from MK and HH; HVRS, A-MRu, HI-S and NM completed qualitative data analysis with support from MK and HH. HVRS, DAR, A-MRu and
    LM drafted the manuscript. All other authors reviewed the manuscript and
    made editorial suggestions. All authors read and approved the final
    manuscript.
    Funding
    This work is supported by the NIHR and UK Research and Innovation,
    administered by the MRC: grant number MR/V02776X/1. The Trial Sponsor is
    the University of Exeter, ref.: 1920/ Research Ethics and Governance Office,
    Lafrowda House, St Germans Road, Exeter, Devon, EX4 6TL. The work is also
    supported by the NIHR Applied Research Collaboration South West
    Peninsula. The views expressed in this publication are those of the authors
    and not necessarily those of the National Institute for Health Research or the
    Department of Health and Social Care. The sponsor and funding sources
    have had no role in the design of this study, nor during the collection,
    analysis, and interpretation of data, nor in writing this manuscript.
    Availability of data and materials
    The datasets used and/or analysed during the current study are available
    from the corresponding author on reasonable request.
    Declarations
    Ethics approval and consent to participate
    This study was granted ethical approval by the University of Exeter Medical
    School Ethics Committee (Application Number Jul20/D/256) and Health
    Research Authority research and development governance assurance (IRAS
    reference 287288). Informed consent to participate in the study was
    obtained electronically from participants at the beginning of the survey. All
    methods were performed in accordance with the relevant guidelines and
    regulations including the Declaration of Helsinki.
    Consent for publication
    Informed consent to publish anonymised participant data was obtained
    electronically from participants at the beginning of the survey.
    Competing interests
    AMRa is President of the Royal College of Nursing. All other authors declare
    that they have no competing interests.
    Author details
    1
    College of Medicine and Health, University of Exeter, St Luke’s Campus,
    Heavitree Road, Exeter EX1 2LU, UK. 2School of Health and Society, University
    Page 16 of 17
    of Salford, Allerton Building, Frederick Rd, Salford M6 6PU, UK. 3Northern Care
    Alliance NHS Group, Stott Lane, Salford M6 8HD, UK. 4Department of Health
    and Caring Sciences, Western Norway University of Applied Sciences,
    Inndalsveien 28, 5063 Bergen, Norway. 5The National Institute for Health
    Research (NIHR) Applied Research Collaboration (ARC) South West Peninsula
    (PenARC), Exeter, UK. 6The Royal Marsden NHS Foundation Trust, Fulham
    Road, London SW3 6JJ, UK. 7School of Medicine, University of Nottingham,
    Queens Medical Centre, Nottingham NG7 2UH, UK. 8Faculty of Nursing,
    Midwifery and Palliative Care, King’s College London, London SE1 8WA, UK.
    9
    NIHR Exeter Clinical Research Facility, Royal Devon and Exeter NHS
    Foundation Trust, Barrack Road, Exeter EX2 5DW, UK. 10Institute of Biomedical
    and Clinical Science, College of Medicine and Health, University of Exeter, St
    Luke’s Campus, Heavitree Road, Exeter EX1 2LU, UK. 11Department of
    Respiratory Science, University of Leicester, University Road, Leicester LE1
    7RH, UK. 12University Hospitals of Leicester NHS Trust, Biomedical Research
    Centre – Respiratory, Glenfield Hospital, Groby Road, Leicester LE3 9QP, UK.
    Received: 18 December 2020 Accepted: 8 October 2021
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    j.1475-6773.2011.01344.x.
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    undertaken in health services research in England: a mixed methods study.
    BMC Health Serv Res. 2007;7(1):85. https://doi.org/10.1186/1472-6963-7-85.
    49. Lavrakas PJ. Encyclopedia of survey research methods. Thousand Oaks: Sage
    Publications; 2008. Available from:. https://doi.org/10.4135/9781412963947.
    50. Bartlett J, Kotrlik J, Higgins C. Organizational research: determining
    appropriate sample size in survey research. Inf Technol Learn Perform J.
    2001;19(1):43–50.
    51. Morse JM. The significance of saturation. Thousand Oaks: Sage; 1995.
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    doi.org/10.1177/1049732315576699.
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    1
    Lab Week 3
    Your Name (without credentials)
    Chamberlain University College of Nursing
    Course Number: Course Name
    Name of Instructor
    Assignment Due Date
    2
    1. Part One Step 1 For our first broad-based search, choose exactly one of the 12
    articles listed that interests you. Use the underlined words in your chosen article
    to search and see how many articles from the Pro-Quest Nursing database contain
    these underlined words. If the Pro-Quest Nursing database is no longer available
    through the Chamberlain Library web site, then please do this instead: “Search
    Entire Chamberlain Collection.” In the gray / grey box below, please clearly
    indicate which of the 12 allowed articles that you have selected for this part of the
    assignment.
    Please disregard this question here based on the new Instructions / Directions.
    Please feel very free to type up your brief article summary here. Thanks much !!
    3
    2. Part One Step 6 Place a screenshot of your search results ( topic and the number
    of articles containing your search terms ) in the gray / grey box below.
    Please disregard this question here based on the new Instructions / Directions.
    4
    3. Part One Step 6 Please answer these questions. Answers must please be within /
    inside this gray / grey box.
    A. On your search, what terms did you use?
    Please disregard this question here based on the new Instructions /
    Directions.
    B. On your search, what other things did you mark on the search page before
    conducting your search?
    Please disregard this question here based on the new Instructions /
    Directions.
    C. On your search, why did you choose the key words that you did?
    Please disregard this question here based on the new Instructions /
    Directions.
    D. On your search, how many articles were found with these search terms ( you find
    this answer on your screen shot submitted on the page just previous here ) ?
    Please disregard this question here based on the new Instructions /
    Directions.
    5
    4. Part Two Step 1 For our second more narrow search, go back and search using
    the entire title of the article you used the key words from in your first search.
    Paste the entire title into the search bar and find the full article ( do not checkmark
    anything to narrow your search this time! ). Find a full text pdf of your chosen
    article. If you have difficulty finding a full text pdf of your chosen article, please
    see Files along the left of the computer screen in the Math 225 course shell /
    template, and then click on Week 3 Files. Click the folder for the Week 3 lab and
    you should be able to find the needed full text pdf. In the gray / grey box below,
    please type the bibliography information for your one specific chosen article,
    using the APA Style Manual seventh edition. What you type into the box below
    will also be an entry in your References list on the last page of this document.
    Please disregard this question here based on the new Instructions / Directions.
    6
    5. Part Two Step 3 In your one specific chosen article, please find ONE frequency
    table and / or ONE graph within the article and place a screenshot of the table and
    / or graph in the gray / grey box below. Thank you !!
    7
    6. Part Two Step 4 Please answer the following question about your table and / or
    graph.
    A. What type of study is used in the article ( quantitative or qualitative or both ) ?
    Answer:
    8
    7. Part Two Step 4 Please answer the following question about your table and / or
    graph.
    B. What type of table and / or graph did you choose for your lab assignment? What
    characteristics or clues or indicators make it this type?
    Answer:
    9
    8. Part Two Step 4 Please answer the following question about your table and / or
    graph.
    C. Describe the data displayed in your chosen table and / or graph. Potentially
    consider class size, class width, total frequency, list of frequencies, class
    consistency, and other elements or factors. Depending on the table and / or graph
    that you chose, many of the things in the list above might not apply, and that is
    OK ! With this question, do the best that you can, given what you have to work
    with. Thank you !!
    Answer:
    10
    9. Part Two Step 4 Please answer the following question about your table and / or
    graph.
    D. Draw a ( tentative and provisional ) conclusion about the data from the table and
    / or graph that you chose.
    Answer:
    11
    10. Part Two Step 4 Please answer the following question about your table and / or
    graph.
    E. How else might these data have been displayed ( OTHER THAN using the table
    and / or graph that you have been using in this assignment ! ) ? Please carefully
    discuss PROS and CONS of TWO OTHER presentation options, such as a
    different table or a different graphical display option choice. Please look
    especially careful at the grading rubric row for this question. Class members
    in the past have struggled a lot with this question. Thanks !!
    Answer:
    12
    11. Part Two Step 4 Please answer the following question about your table and / or
    graph.
    F. Please give the full APA Style Manual seventh edition reference of the specific
    chosen article that you are using for this lab assignment. This is simply a repeat
    of the answer you gave in Question 4. further above in this assignment document.
    Answer:
    13
    References
    Type your references here using hanging indent and double line spacing (under
    “Paragraph” on the Home toolbar ribbon). See your APA Manual ( seventh edition ) and
    the resources in the APA section of Resources for reference formatting.

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