Gender Dysphoria and Transition
DyGePeT
1 other identifier
observational
10
0 countries
N/A
Brief Summary
Persons with gender dysphoria present the difficulties of access to health care. Little time is devoted to education of health professionals about the care of transgender persons. According to the proposal of the French Ministry of Social Affairs and Health there is a need to increase knowledge in this area and to improve the care of transgender people including prevention and screening. Similarly, little is known about social and medical needs of the transgender population. This project proposes to illustrate gender dysphoria through testimonies of transgender people with the aim to increase the investigator's understanding aout the needs and the desires of this population and to describe the process of medical and social transition.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Oct 2020
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 10, 2020
CompletedFirst Posted
Study publicly available on registry
February 12, 2020
CompletedStudy Start
First participant enrolled
October 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2021
CompletedAugust 11, 2020
July 1, 2020
8 months
February 10, 2020
August 7, 2020
Conditions
Outcome Measures
Primary Outcomes (1)
Illustrate the real-life experiences of transgender people
4 months
Interventions
guided interview
Eligibility Criteria
The participation to the study will be offered consecutively to adult subjects with gender dysphoria followed in the department of endocrinology, diabetology and nutrition of the University Hospital of Nancy.
You may qualify if:
- Person affiliated to a social security system
- Person having received complete information on the organisation of the research and having signed the informed consent
- Person having carried out a prior clinical examination adapted to the research
- Age\> 18 years
- Diagnosis of gender incongruence (dysphoria) according to the international classification of diseases, revision 11
You may not qualify if:
- Severe, uncontrolled psychiatric or somatic illness
- Substance and alcohol addiction
- Pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Central Hospital, Nancy, Francelead
- University of Lorrainecollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- FAMILY BASED
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 10, 2020
First Posted
February 12, 2020
Study Start
October 1, 2020
Primary Completion
June 1, 2021
Study Completion
September 1, 2021
Last Updated
August 11, 2020
Record last verified: 2020-07