TransgenderismParTransRepNCT06221163
Sociological Study of the Life Courses of Young TRANSgender Patients
An observational study of Transgenderism, run by Central Hospital, Nancy, France.
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… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Transgenderism
- What is being tested?
- collection of biographical and sociological data
- How many people
- 30 participants
- Where
- No sites listed yet
- Study dates
- Apr 2024to Nov 2024
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Young transgender people
Who may be able to join
- transgender
Who cannot join
- Refusal by the patient.
- Refusal by the patient's legal guardian.
- Person under guardianship
About this study
Official title: Sociological Study of the Life Courses of Young TRANSgender Patients Consulting the REProduction Medicine Department
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.
Read the detailed 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.
- Conditions
- Transgenderism
- Being tested
- collection of biographical and sociological data
- Medical subject headings
- Transsexualism
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
collection of biographical and sociological dataOther
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).
| Study group | Role | What they receive |
|---|---|---|
| Young transgender | Transgender patients consulting the Reproductive Medicine Department for a request related to the preservation of their fertility or hormone therapy, as well as parents/family members present at the time of the appointment.
The ceiling is 20 interviews and 80 hours. Receives: Other: collection of biographical and sociological data |
What is being measured
The primary outcome is the main question the study is designed to answer.
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).
Measured: 1 year
Secondary outcomes (1)
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.
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Jan 2024
- Study startApr 2024 (estimated)
- Primary completionAug 2024 (estimated)
- Study completionNov 2024 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for TransgenderismStudies of the same condition, open and under way.
- More trials run by Central Hospital, Nancy, FranceThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Other
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Central Hospital, Nancy, France
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Mikael AGOPIANTZ, Central Hospital, Nancy, France
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06221163
- Sponsor's protocol ID
- 2023PI015
- Acronym
- ParTransRep
- Status last verified
- Jan 2024
- First submitted
- 6 Apr 2023
- Last updated
- 24 Jan 2024
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Jan 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Sociological Study of the Life Courses of Young TRANSgender Patients Consulting the REProduction Medicine Department
- ClinicalTrials.gov ID
- NCT06221163
- Acronym / sponsor ID
- ParTransRep / 2023PI015
- Conditions
- Transgenderism
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- Central Hospital, Nancy, FranceUniversity, hospital or other
- Study start
- Apr 2024 (estimated)
- Primary completion
- Aug 2024 (estimated)
- Study completion
- Nov 2024 (estimated)
- First posted
- 24 Jan 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed 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.
Study design
- Observational model
- Other
- Time perspective
- Other
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Young transgender | – | Other: collection of biographical and sociological dataTransgender patients consulting the Reproductive Medicine Department for a request related to the preservation of their fertility or hormone therapy, as well as parents/family members present at the time of the appointment. The ceiling is 20 interviews and 80 hours. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Young transgender people
Key inclusion criteria (1 listed)
- transgender
Key exclusion criteria (3 listed)
- Refusal by the patient.
- Refusal by the patient's legal guardian.
- Person under guardianship
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| collection of biographical and sociological datacollection 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). | Other | Young transgender |
Primary outcome
Ethnographic observations of consultations to study relation to care pathway for transgender people
Time frame: 1 year
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 secondary outcome
Ethnographic observations of transgender consultations in the Reproductive Medicine Department
Time frame: 1 year
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jan 2024.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Transgenderism, run by Central Hospital, Nancy, France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 24 Jan 2024. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Ethnographic observations of consultations to study relation to care pathway for transgender people (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jan 2024.