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NCT06221163 Clinical Trial

Sociological Study of the Life Courses of Young TRANSgender Patients

Transgenderism Clinical Trial

— ParTransRep  

Official title:
Sociological Study of the Life Courses of Young TRANSgender Patients Consulting the REProduction Medicine Department

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06221163
Other study ID # 2023PI015
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 2024
Est. completion date November 2024

Study information
Verified date January 2024
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The number of people consulting for a request related to trans identity is increasing sharply. The study monocentric qualitative study of discursive material aims to describe the diversity of practices and discourses mobilized by the people concerned and their relatives in the wake of work already carried out in the human sciences. Conducting non-directive interviews (life stories) with transgender patients consulting the Reproductive Medicine Department and their volunteer relatives.The ceiling is 20 interviews and 80 hours of observation.

Description:

The number of people consulting for a request related to trans identity is increasing sharply. The study aims to describe the diversity of practices and discourses mobilized by the people concerned and their relatives in the wake of work already carried out in the human sciences. The care pathway is a central determinant of transgender experiences and differentiated care pathways indicate differentiated relationships to medicalisation and gender, which translate into practices. For the moment, transgender people who do not wish to preserve their fertility or who are not hormonally treated are over-represented in the sample. It is extremely important to gain access to the population that turns to the Reproductive Medicine Service. The consultation is a place where knowledge (medical, activist, etc.) circulates and meets, which can then be re-appropriated or negotiated by transgender people. While interviews alone are not enough to describe this re-appropriation and negotiation, it is possible to do so through observations of consultations. Conducting non-directive interviews (life stories) with transgender patients consulting the Reproductive Medicine Department and their volunteer relatives. The ceiling is 20 interviews and 80 hours of observation. Patients are given a 'flyer' at the time of their consultation on which the interviewer's contact details are given. They are free to contact the interviewer to find out when and where an interview might take place (outside hospital). The ceiling is 20 interviews and 80 hours of observation. Discussions during the interview are recorded using a voice recording device, then transcribed in full in Word and anonymised. Discussions during consultations were recorded using notes, then formatted in Word and anonymised.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 30
Est. completion date November 2024
Est. primary completion date August 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - transgender Exclusion Criteria: - Refusal by the patient. - Refusal by the patient's legal guardian. - Person under guardianship

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• collection of biographical and sociological data
collection of biographical and sociological data. Conducting non-directive interviews (life stories) with transgender patients consulting the Reproductive Medicine Department and their volunteer relatives. Patients are given a 'flyer' at the time of their consultation on which the interviewer's contact details are given. They are free to contact the interviewer to find out when and where an interview might take place (outside hospital).

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Central Hospital, Nancy, France

Outcome
Type Measure Description Time frame Safety issue
Primary Ethnographic observations of consultations to study relation to care pathway for transgender people Conducting non-directive interviews (life stories) with transgender patients consulting the Reproductive Medicine Department and their volunteer relatives. Patients are given a flyer at the time of their consultation on which the interviewer's contact details are given. They are free to contact the interviewer to find out when and where an interview might take place (outside hospital). 1 year
Secondary Ethnographic observations of transgender consultations in the Reproductive Medicine Department Ethnographic observations of consultations in the Reproductive Medicine Department. The investigator is present during consultations with transgender patients and takes notes of what he observes and hears. He ensures that those present give their informed consent at the start of the appointment. 1 year
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