- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05684783
Dementia Champions in Homecare (DemChamp)
October 5, 2023 updated by: King's College London
Developing the Role of Dementia Champions in the Homecare Sector
This is a descriptive, explorative study in which we will explore how the role of Dementia Champions in homecare services could develop, and become more widely implemented in this sector's workforce.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This study had three parts:
- The investigators will start by learning from the work of other Dementia Champions working across care services to get a 'real world' in-depth understanding of what working as a Dementia Champion involves, what works well, and what can be improved. The investigators will carry out qualitative interviews with care professionals with experience of being or working with Dementia Champions. They will also speak to people affected by dementia (people living with dementia and their family carers) who have received care from services with Dementia Champions.
- The investigators will carry out a stakeholder consultation workshop with 10 people including care professionals, people affected by dementia, and other relevant stakeholders, to build on what we have learned so far. They will commission a Science Illustrator to visually scribe the workshop discussions and produce an illustration of the Dementia Champion in homecare role.
- The investigators will use the model created in part 2 of the study to facilitate interviews in part 3. They will speak to staff working in homecare services (managers and homecare workers) that do not have Dementia Champions in them, and people living with dementia and family members who use homecare services that do not have Dementia Champions in them. This will help the research team understand how to better establish the role of Dementia Champions and how this could work within homecare, including what would be needed to support staff in this role.
Study Type
Observational
Enrollment (Estimated)
80
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Tiffeny James, PhD
- Phone Number: 0044 (+44) 207 848 1782
- Email: tiffeny.james@kcl.ac.uk
Study Contact Backup
- Name: Monica Leverton, PhD
- Phone Number: 0044 (+44) 207 848 1782
- Email: monica.leverton@ucl.ac.uk
Study Locations
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-
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South Molton, United Kingdom
- Recruiting
- Home Instead Devon
-
Contact:
- Adam Crispin
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Participants from England, Scotland, Wales, or Northern Ireland who either, recruited from health or social care settings.
Description
Inclusion criteria
Part 1 (group 1 interviews):
- Staff who are or have been DCs in services that provide care and support to people affected by dementia
- Staff who work or have worked alongside DCs in services that provide care and support to people affected by dementia
- Staff with expertise in dementia e.g. those from third sector or voluntary dementia organisations
- A person living with dementia who receives or has received support or care from services with DCs embedded within the team i.e., homecare
- A current or former family carer of a person living with dementia who receives or has received support or care from services with DCs embedded within the team i.e., homecare
Part 2 (stakeholder consultation workshop):
- Homecare staff (including any DCs identified from previous study phases)
- Dementia specialists (e.g., social workers with expertise in dementia, Admiral Nurses)
- People living with dementia in receipt of homecare support
- Current or former family carers of a person living with dementia in receipt of homecare support
- Any other relevant care staff
Part 3 (group 2 interviews):
- A homecare worker, manager, or other member of homecare staff
- A person living with dementia in receipt of homecare support
- A current or former family carer of a person living with dementia in receipt of homecare
Exclusion Criteria:
- People who do not have capacity to consent to take part in this research study. The research team has experience of conducting informal assessments of capacity, using the three-stage test outlined in the Mental Capacity Act 2005 of England and Wales.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
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Group 1 interviews
Care professionals with experience of being or working with Dementia Champions, and people affected by dementia who have received care from services with Dementia Champions.
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Group 2 interviews
Homecare professionals working in services where there are no Dementia Champions, and people affected by dementia who have received care from services with no Dementia Champions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
This is a qualitative study involving interviews and as such, there are no measurable outcomes. We will, however, use an interview topic guide to conduct interviews, and use the findings to produce a Model of Dementia Champions in the homecare sector
Time Frame: 8 months
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Experiences of care staff, people living with dementia, and family carers of dementia champions in homecare.
|
8 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Monica Leverton, King's College London
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 26, 2023
Primary Completion (Estimated)
October 1, 2023
Study Completion (Estimated)
December 1, 2023
Study Registration Dates
First Submitted
December 13, 2022
First Submitted That Met QC Criteria
January 12, 2023
First Posted (Actual)
January 13, 2023
Study Record Updates
Last Update Posted (Actual)
October 6, 2023
Last Update Submitted That Met QC Criteria
October 5, 2023
Last Verified
December 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRAS 320561
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
If participants agree to their interview data being used for future ethically approved research by King's College London then we will make this available to other King's College London researchers.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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