The goal of this single-arm feasibility study is to evaluate the feasibility and acceptability of an 8-week mindful self-compassion intervention and associated data-collection plan among transgender and nonbinary young adults. Participants will be asked to: * Complete weekly 2.5-hour virtual classes for 8 weeks and a 4-hour virtual retreat * Practice specific activities in between classes for 20-30 minutes a day * Answer survey questions before starting the intervention, half-way through the intervention, after the intervention, and 3-months after the intervention ends.
Age range
18 Years – 29 Years
Sex
ALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
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.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Recruitment of participants into study
Timeframe: immediately after the intervention
Percent of Sample Completing the Intervention
Timeframe: immediately after the intervention
Percent of participants who report satisfaction with MSC as Excellent or Good
Timeframe: immediately after the intervention, at 12-week follow-up
Likelihood of recommending to others
Timeframe: immediately after the intervention, at 12-week follow-up
Intent to use specific intervention activities in the future
Timeframe: immediately after the intervention
Percent of completed data at each data-collection point
Timeframe: baseline, intervention week 4, immediately after the intervention, and 12 weeks after the intervention is completed