- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05339191
Compassionate Imagery for People With An Intellectual Disability
A Brief Compassionate Imagery Intervention for People With an Intellectual Disability: A Case Series in a Clinical Setting
The current study aims to explore the adaptation of compassionate imagery for people with an intellectual disability who are experiencing mental health difficulties. It will explore whether participants are able to generate and use their own compassionate image, as well as exploring the participants' views of engaging in the workshop. It is an early exploratory study in what is hoped will be a longer process consisting of future feasibility and piloting work.
Between 6-10 participants who are attending the National Health Service (NHS) NHS Lanarkshire Community Learning Disability Team and are experiencing mental health difficulties will be recruited. Participants will be asked to attend a two-session workshop through which they will be supported to develop and use their own compassionate image. The research questions will be answered by obtaining descriptive data from data recording sheets completed during the sessions and by interviewing participants about their experiences of the workshop.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
People with an intellectual disability experience widespread stigma, mistreatment and abuse (Scior and Werner, 2016, Gravell, 2012, Hughes et al., 2012, Jones et al., 2012). These are likely to lead individuals to experience shame and self-criticism, which can contribute to the development of mental health difficulties. Indeed, many people with an intellectual disability do experience mental health difficulties (Buckles et al., 2013).
Compassion-Focused Therapy (CFT) is a psychological therapy which aims to reduce shame and self-criticism by developing a person's ability to feel compassion. It involves enabling individuals to learn to soothe themselves when they feel distressed. Compassionate imagery is one CFT technique used to do this (Gilbert, 2009). This can involve developing a mental image of a compassionate person or animal who is wise, strong, warm and non-judgemental.
The individual is encouraged to explore their experience of imagining this, which may include feeling a sense of safety, warmth and connectedness (Gilbert, 2015).
The current study aims to explore the adaptation of compassionate imagery for people with an intellectual disability who are experiencing mental health difficulties. It will explore whether participants are able to generate and use their own compassionate image, as well as exploring the participants' views of engaging in the workshop. It is an early exploratory study in what is hoped will be a longer process consisting of future feasibility and piloting work.
Between 6-10 participants who are attending the NHS Lanarkshire Community Learning Disability Team and are experiencing mental health difficulties will be recruited. Participants will be asked to attend a two-session workshop through which they will be supported to develop and use their own compassionate image. The research questions will be answered by obtaining descriptive data from data recording sheets completed during the sessions and by interviewing participants about their experiences of the workshop.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Lanarkshire
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Kilsyth, Lanarkshire, United Kingdom, G65 4JE
- Kilsyth Community Centre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Open to NHS Lanarkshire's Community Learning Disability Team (CLDT) and will therefore be aged 16 or above
- Experiencing mental health difficulties
Exclusion Criteria:
- Do not have capacity to provide informed consent
- Have insufficient communication skills to engage with the tasks
- Have sensory impairments which are likely to inhibit their ability to engage with the study materials
- Actively suicidal
- Likely to be disruptive or distressed in a group setting
- Known to have previously engaged in a piece of therapeutic work involving the development of a compassionate image
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Compassionate image workshop
Participants attend a workshop through which they will be supported to develop and use their own compassionate image.
|
Participants attend a workshop through which they will be supported to develop and use their own compassionate image.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compassionate image
Time Frame: 6 months
|
Number of participants that are able to generate their own compassionate image
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-soothing
Time Frame: 6 months
|
Number of participants that report using their compassionate image to self-soothe outside of sessions and the number that find this to be helpful.
|
6 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Miriam Holm, NHS Lanarkshire
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- L19092
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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