A Self-compassion Intervention for LGBTQ+ Individuals (NCT06691282) | Clinical Trial Compass
CompletedNot Applicable
A Self-compassion Intervention for LGBTQ+ Individuals
Hong Kong17 participantsStarted 2024-12-21
Plain-language summary
Gender and sexual minorities often face minority stress, leading to body dissatisfaction and potential psychological issues like anxiety and depression. Self-compassion has been identified as an effective strategy for managing emotions during negative experiences and may serve as a protective factor against minority stress and body image concerns. However, research on self-compassion interventions specifically for LGBTQ+ individuals is limited. This study aims to evaluate the feasibility, acceptability, and preliminary effectiveness of a self-compassion intervention to enhance body image and psychological well-being among LGBTQ+ individuals in Hong Kong.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Aged 18 years or above;
* Self-identified as LGBTQ+;
* Able to speak, read, and write Cantonese or Putonghua;
* Willing to participate in the study and share their experience of the intervention with the research team;
* Provide written informed consent to participate in the study.
Exclusion Criteria:
* Current psychosis or intellectual disability;
* Current suicidal ideation with intent (score ≥ 4) as measured using the Columbia suicide severity rating scale;
* Participation in similar studies.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Self-compassion
Timeframe: Through study completion, on average 4 weeks
2
Internalized stigma
Timeframe: Through study completion, on average 4 weeks