Improving Wellbeing and Health for Care Home Residents During COVID-19 (COVIDWHELD)
Primary Purpose
Dementia
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
COVID WHELD
Sponsored by
About this trial
This is an interventional treatment trial for Dementia
Eligibility Criteria
Inclusion Criteria:
Care homes which include people with dementia within their client group
All individuals residing in participating care homes who meet diagnostic criteria for dementia and/or score '1' or greater on the Clinical Dementia Rating Scale.
Exclusion Criteria:
Care homes under special measures with the local authority
Residents from whom consent or the advice of a consultee cannot be obtained.
Sites / Locations
- University of ExeterRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
WHELD training/virtual coaching programme supported with digital resources
Treatment as Usual
Arm Description
WHELD training/virtual coaching programme supported with digital resources
Usual Best practice
Outcomes
Primary Outcome Measures
Dementia Quality of Life - DEMQOL proxy
Validated quality of life measure for people with dementia, assessed by informant interview. Minimum score = 32 Maximum score = 128; Higher score denotes better outcome.
Secondary Outcome Measures
Neuropsychiatric Inventory
Standardized assessment of neuropsychiatric symptoms in people with dementia, assessed by informant interview. Minimum score = 0 Maximum score = 144; Higher score denotes worse outcome.
Psychotropic medications
Use of antipsychotic and other psychotropic medications from prescribing charts
Confidence in Dementia (CODE) Scale
Staff confidence measure, self completed questionnaire. Minimum score = 9 Maximum score = 45; Higher score denotes better outcome.
Sense of Competence in Dementia Care Staff (SCIDS) scale
Perceived self efficacy of care staff, self completed questionnaire. Minimum score = 17 Maximum score = 68; Higher score denotes better outcome.
Patient Health Questionnaire (PHQ-9)
Mental Health of care staff, self reported questionnaire. Minimum score = 0 Maximum score = 27; Higher score denotes worse outcome.
EQ5D (Euroquol 5D - 5 dimensions)
A standardized instrument for measuring generic health related quality of life, used for Health economic evaluation. Visual Analogue scale minimum score = 0, maximum score = 100. Higher score denotes better outcome.
Client Service Receipt Inventory
to collect service utilization data for health economics. Assesses cost of service provision; as such no min/max values. Higher value denotes worse cost outcome.
Full Information
NCT ID
NCT04590469
First Posted
October 13, 2020
Last Updated
May 25, 2021
Sponsor
University of Exeter
Collaborators
King's College London, London School of Economics and Political Science, University of East Anglia, University of Hull, Alzheimer's Society
1. Study Identification
Unique Protocol Identification Number
NCT04590469
Brief Title
Improving Wellbeing and Health for Care Home Residents During COVID-19
Acronym
COVIDWHELD
Official Title
Evidence-Based Supported Digital Intervention for Improving Wellbeing and Health of People Living in Care Homes and Care Home Staff (WHELD) During COVID-19: An RCT to Evaluate COVID-19 Adapted E-WHELD: Benefits and Cost-Effectiveness
Study Type
Interventional
2. Study Status
Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
December 1, 2021 (Anticipated)
Study Completion Date
January 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Exeter
Collaborators
King's College London, London School of Economics and Political Science, University of East Anglia, University of Hull, Alzheimer's Society
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
More than 400,000 people in the UK live in care homes. These individuals are particularly vulnerable to COVID-19; many are frail and the majority have concurrent physical health problems and dementia. This group are at the highest risk of becoming severely ill with COVID-19 and are dependent on a stretched care workforce. The isolation, together with the stresses and distressing nature of the current work environment is also likely to have an impact on the mental health and well-being of care staff. It is vital to provide good quality support to enable care staff to remain resilient, and to enable good quality care that maintains the well-being of residents with dementia and reduces emerging neuropsychiatric symptoms in residents without increasing harmful sedative medications.
COVID E-WHELD is based on the optimized WHELD training intervention on successfully completed in randomised clinical trials (RCTs) in 86 care homes, more than 1000 people with dementia. WHELD reduced use of anti-psychotics, improved agitation and overall neuropsychiatric symptoms, improved quality of life and reduced mortality for people with dementia. A digital version of WHELD (eWHELD) with virtual supervision in a further care home RCT including 130 people with dementia has demonstrated benefits for staff carers and improvements in the quality of life of people with dementia, with eWHELD combined with virtual supervision, but not with e-learning alone.
The current project will evaluate a COVID-19 adapted version of eWHELD to address current needs of care homes during the COVID-19 pandemic. This will be undertaken in a 2 arm, 4 month, randomized cluster RCT in 1280 care homes (allowing for 75% drop out with COVID-19 outbreaks) to determine whether COVID-19 adapted eWHELD improves quality of life and mental health for people with dementia in care homes and the mental health of care staff.
Detailed Description
COVID E-WHELD: Effectiveness and Cost-Effectiveness
COVID-19 adapted WHELD (with digital resources and virtual coaching) will be compared to usual care in a 4 month randomized, parallel group, cluster RCT with 1280 care homes (allowing for 75% drop out because of COVID-19 outbreaks). Care homes will be randomly assigned to WHELD or treatment as usual in a 1:1 ratio. All care homes receiving treatment as usual will be offered the WHELD intervention after 4 months.
Recruitment will build upon a number of networks and contacts. The investigators already have a network of more than 1300 care homes who would be our first point of contact (100 additional care homes from Biomedical Research Centre (BRC) care home network. The investigators have a long established and successful record of recruiting large numbers of care homes to clinical trials (WHELD programme, FITS programme, Pimavanserin programme which involved more than 160 care homes).
Evaluation will be undertaken at baseline, 4 weeks and 4 months post-baseline.
The primary outcome measure will be quality of life in care home residents at 4 months, measured by the DEMQOL proxy, which has shown significant benefits in previous WHELD RCTs. The secondary outcomes will include cost-effectiveness (EQ-5D), health utilization, use of sedative medications (anti psychotics, hypnotics), neuropsychiatric symptoms, staff confidence (CODE), staff self-efficacy (SCIDS) and staff mental health (PHQ9) and a COVID-19 tracker.
Process measures collected by coaches will include Goal Attainment,
Assessments will be conducted by telephone or Microsoft Teams, by trained Research Assistants, or with the added option of being collected digitally for staff self-report measures.
Data will also be collected on numbers of remote health and social care (HSC) consultations and on unplanned hospital attendances/admissions (including fall-related injuries). Researchers will also fully cost the COVID eWHELD intervention. To examine the opportunity costs of the intervention, champions will be asked to identify activities that were not undertaken in order to participate and to report any paid and unpaid overtime related to time spent in the champion role. Unit costs will be obtained from nationally applicable sources (PSSRU UC, NHS Reference costs) or calculated anew where necessary.
Key elements of the WHELD intervention include:
Coaching/training to deliver the WHELD programme which includes person-centred care and person-centred activities and person-centred care plans.
A COVID-19 specific resource toolkit - digital bite-sized practical content to stay connected, develop new routines, how to respond to virus-related fear and anxiety
Facilitated online peer support network for care home managers to share stories and solutions for COVID-19 challenges
Pooling insights from others to create short, digestible digital resources, such as: checklists, video tips, one-page guides, do's and don'ts, infographics, etc.
Providing communal, collaborative online group supervision calls, to promote staff well-being and peer-to-peer communities in an online gathering place
Developing easy reference guides to enable staff to support residents, where appropriate, to use virtual communication tools to stay connected with family and friends
Providing a series of suggestions, activities, and games all designed to foster connection during a time of isolation
As the intervention is optimized best practice, the researchers would consider this activity as service delivery and not research. The research element is the evaluation of potential benefits for residents and staff, and the evaluation of cost-effectiveness.
Analyses and reporting will follow CONSORT guidance. A full statical analysis plan will be developed during the initial phases of the project and signed off prior to database lock.
The UK Clinical Research Collaboration (UKCRC)-registered Exeter Clinical Trials Unit will be fully involved in the design, management and governance of the RCT aspects of the trial. The unit will have input into the methodology, provide central trial management/senior oversight, build and test the required data collection systems, undertake randomization, manage the data and ensure a surrounding quality assurance framework.
Care homes will specifically be able to pause participation in the study if there is a COVID-19 outbreak in the care home.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
4 month, randomized, parallel group cluster RCT comparing the WHELD nursing home programme with virtual coaching and digital support with treatment as usual
Masking
Outcomes Assessor
Masking Description
The intervention is a care home/nursing home training programme/coaching and a digital platform. The research assistants collecting data will do so using virtual platforms and will not be told the randomization of participating care homes. Participating care homes will be told not to disclose treatment allocation, and this will be reinforced by the research assistant at the start of each research assessment to maintain the blind.
Allocation
Randomized
Enrollment
2880 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
WHELD training/virtual coaching programme supported with digital resources
Arm Type
Experimental
Arm Description
WHELD training/virtual coaching programme supported with digital resources
Arm Title
Treatment as Usual
Arm Type
No Intervention
Arm Description
Usual Best practice
Intervention Type
Other
Intervention Name(s)
COVID WHELD
Intervention Description
COVID WHELD is a COVID-19 adapted version of an established nursing home training intervention that confers benefits in well-being and neuropsychiatric symptoms for people with dementia. The adaptations include the development of digital resources to support the programme and virtual coaching.
Primary Outcome Measure Information:
Title
Dementia Quality of Life - DEMQOL proxy
Description
Validated quality of life measure for people with dementia, assessed by informant interview. Minimum score = 32 Maximum score = 128; Higher score denotes better outcome.
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Neuropsychiatric Inventory
Description
Standardized assessment of neuropsychiatric symptoms in people with dementia, assessed by informant interview. Minimum score = 0 Maximum score = 144; Higher score denotes worse outcome.
Time Frame
4 months
Title
Psychotropic medications
Description
Use of antipsychotic and other psychotropic medications from prescribing charts
Time Frame
4 months
Title
Confidence in Dementia (CODE) Scale
Description
Staff confidence measure, self completed questionnaire. Minimum score = 9 Maximum score = 45; Higher score denotes better outcome.
Time Frame
4 months
Title
Sense of Competence in Dementia Care Staff (SCIDS) scale
Description
Perceived self efficacy of care staff, self completed questionnaire. Minimum score = 17 Maximum score = 68; Higher score denotes better outcome.
Time Frame
4 months
Title
Patient Health Questionnaire (PHQ-9)
Description
Mental Health of care staff, self reported questionnaire. Minimum score = 0 Maximum score = 27; Higher score denotes worse outcome.
Time Frame
4 months
Title
EQ5D (Euroquol 5D - 5 dimensions)
Description
A standardized instrument for measuring generic health related quality of life, used for Health economic evaluation. Visual Analogue scale minimum score = 0, maximum score = 100. Higher score denotes better outcome.
Time Frame
4 months
Title
Client Service Receipt Inventory
Description
to collect service utilization data for health economics. Assesses cost of service provision; as such no min/max values. Higher value denotes worse cost outcome.
Time Frame
4 months
Other Pre-specified Outcome Measures:
Title
Goal Attainment Scaling
Description
Ordinal scale to rate progress towards personalized goals for people with dementia as a process outcome. Scale for each goal: Minimum score = 1 Maximum score = 4; Higher score denotes better outcome.
Time Frame
4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Care homes which include people with dementia within their client group
All individuals residing in participating care homes who meet diagnostic criteria for dementia and/or score '1' or greater on the Clinical Dementia Rating Scale.
Exclusion Criteria:
Care homes under special measures with the local authority
Residents from whom consent or the advice of a consultee cannot be obtained.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Clive G Ballard, MD
Phone
00441392 72 2805
Email
c.ballard@exeter.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Dag Aarsland, MD
Phone
44 20 7848 0508
Email
dag.aarsland@kcl.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clive Ballard, MD
Organizational Affiliation
The University of Exeter
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Exeter
City
Exeter
State/Province
Devon, UK
ZIP/Postal Code
EX1 2LU
Country
United Kingdom
Individual Site Status
Recruiting
12. IPD Sharing Statement
Citations:
PubMed Identifier
29408901
Citation
Ballard C, Corbett A, Orrell M, Williams G, Moniz-Cook E, Romeo R, Woods B, Garrod L, Testad I, Woodward-Carlton B, Wenborn J, Knapp M, Fossey J. Impact of person-centred care training and person-centred activities on quality of life, agitation, and antipsychotic use in people with dementia living in nursing homes: A cluster-randomised controlled trial. PLoS Med. 2018 Feb 6;15(2):e1002500. doi: 10.1371/journal.pmed.1002500. eCollection 2018 Feb.
Results Reference
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PubMed Identifier
16543297
Citation
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Results Reference
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Citation
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Results Reference
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Citation
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Results Reference
result
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Improving Wellbeing and Health for Care Home Residents During COVID-19
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