Compassionate Imagery for People With An Intellectual Disability

April 14, 2022 updated by: NHS Lanarkshire

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

Completed

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

Interventional

Enrollment (Actual)

4

Phase

  • Not Applicable

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

    • Lanarkshire
      • Kilsyth, Lanarkshire, United Kingdom, G65 4JE
        • Kilsyth Community Centre

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

16 years to 100 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

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

  • 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

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Investigators

  • Principal Investigator: Miriam Holm, NHS Lanarkshire

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)

July 1, 2020

Primary Completion (Actual)

April 30, 2021

Study Completion (Actual)

April 30, 2021

Study Registration Dates

First Submitted

April 14, 2022

First Submitted That Met QC Criteria

April 14, 2022

First Posted (Actual)

April 21, 2022

Study Record Updates

Last Update Posted (Actual)

April 21, 2022

Last Update Submitted That Met QC Criteria

April 14, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

None will be shared

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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