- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06508853
Transforming Care Experiences of Support Workers and Managers
July 15, 2024 updated by: King's College London
Exploring the Experience of Support Workers and Managers Supporting People With Learning Disabilities Who Have Moved From Inpatient to Community Settings as Part of the Transforming Care Agenda.
- What research question is being addressed? What is the experience of support workers, and managers, supporting people with learning disabilities who have moved from inpatient to community settings as part of the Transforming Care Agenda.
- How is it of relevance and importance to patients and public? In 2011 serious abuse of people with learning disabilities was uncovered at Winterbourne View, an independent hospital for people with learning disabilities. The Transforming Care Agenda was set out by the UK government in 2012 in response to this abuse. A key part of the action plan included moving people with learning disabilities out of inappropriate hospital settings, into the community.
Support workers and managers are key mediators in approaches to ensure that people with learning disabilities are able to achieve a good quality of life in the community, however so far there is limited research looking into their experiences.
- Broadly what area (disease, therapy or service) is being studied? For therapeutic studies what is the drug, device or procedure being tested? The area being studied is support for people with learning disabilities who have moved from inpatient settings to community settings.
- Who would be eligible? Support workers and managers who have worked with people with learning disabilities who have moved from inpatient to community settings within the past three years will be eligible to be interviewed as part of this study. 4 to 6 support workers, and 4 to 6 managers will be interviewed in total.
- The type of sites where the study will be conducted Participants (support workers and managers) will be recruited through NHS sites (community learning disability teams) who have identified individuals with learning disabilities who have moved from hospital to community settings (as part of the Transforming Care Agenda) within the past 3 years.
- How long will the study last and what will the participants undergo? The study will last approximately 1.5 years. If they consent, participants will be invited to take part in an interview, lasting up to one hour. The interview will focus on their experience of supporting someone with a learning disability who has moved from a hospital setting, into a community setting, within the past three years.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
12
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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London, United Kingdom
- Kings College London
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Contact:
- Kate Blamires
- Email: kate.blamires@kcl.ac.uk
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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
Yes
Sampling Method
Non-Probability Sample
Study Population
Participants will be support workers and managers working with people with learning disabilities who have moved from hospital to community settings as part of the transforming care agenda.
Description
Inclusion Criteria:
- Participants will be support workers and managers working within services for people with learning disabilities (supported living or care home settings).
- Participants need to have worked with someone who has a learning disability who has been discharged from hospital during the past three years.
- Participants need to have worked with the person with a learning disability during the first three years of their discharge from hospital.
- Participants need to have worked with the person who has a learning disability for a period of at least four months.
- The person with a learning disability will need to have been discharged from hospital, into their current service, within the past 3 years.
- For each person with a learning disability identified, a maximum of two support workers and one manager can be included (interviewed).
- Support workers or managers will need to be based within one of the four research site localities (South London and Maudsley, Hertfordshire NHS University Trust, East London Foundation Trust and North East London Foundation Trust).
- Support workers and managers will need to be able to participate in interviews on Microsoft Teams, or in person, conducted in the English language.
- There are no inclusion or exclusion criteria based on age, gender, ability or any other personal identifiers.
Exclusion Criteria:
- Support workers or managers working with autistic people, or people who have experienced mental health difficulties (without a learning disability).
- Support workers or managers who have worked with the person with a learning disability for less than four months.
- Support workers or managers working in locations outside of the remit of any of the four research sites.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
No formal outcome measures - qualitative analysis of data from interviews.
Time Frame: 1
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Data will be analysed using IPA
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1
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
August 1, 2024
Primary Completion (Estimated)
March 1, 2025
Study Completion (Estimated)
May 1, 2025
Study Registration Dates
First Submitted
July 15, 2024
First Submitted That Met QC Criteria
July 15, 2024
First Posted (Actual)
July 18, 2024
Study Record Updates
Last Update Posted (Actual)
July 18, 2024
Last Update Submitted That Met QC Criteria
July 15, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 339318
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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