Cohort Study on Factors Associated with the Evolution of Quality of Life Among Transgender Indivi… (NCT06854965) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Cohort Study on Factors Associated with the Evolution of Quality of Life Among Transgender Individuals in the French Population
France1,500 participantsStarted 2025-02-28
Plain-language summary
This research focuses on identifying medical, social, and healthcare journey determinants associated with the evolution of quality of life in the transgender population at 12 months. To address the research question, it is planned to include 1,500 transgender individuals, among those attending healthcare professionals or associations in the French territory who have agreed to take on the role of investigators (professionals in healthcare or designated individuals within an association).
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:
* Person identifying themselves as trans
* Person of legal age (≥ 18 years)
* Person living in France
* Person who has not expressed any opposition after receiving full information about the protocol
* Person who understands and speaks French, or who is an allophone speaking English, Spanish or Portuguese
Exclusion Criteria:
* People who do not understand or speak French, English, Spanish or Portuguese.
* Person under guardianship or curatorship, under legal protection or under safeguard of justice
* Anyone who has expressed their opposition after receiving full information about the protocol.
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
Change in quality of life (WHOQOL-BREF) between 0 and 12 months.
Timeframe: From enrollment to the last questionnaire at 12 months