Expectations and Beliefs of Transgender People Regarding Hormonal Treatment

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Recruiting
CT.gov ID
NCT05474768
Collaborator
(none)
20
1
10.9
1.8

Study Details

Study Description

Brief Summary

Hormonal treatment of gender dysphoria can have repercussions on metabolism, cardiovascular system and fertility and represents à potential oncological risk. According to the recommendations of the Endocrine society. Therefore, initial assessment and follow-up visits are necessary and must be carried out to avoid the apparition of potentially undesirable effects.

Condition or Disease Intervention/Treatment Phase
  • Other: no intervention

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Expectations and Beliefs of Transgender People Regarding Hormonal Treatment
Actual Study Start Date :
Feb 2, 2022
Anticipated Primary Completion Date :
Nov 1, 2022
Anticipated Study Completion Date :
Jan 1, 2023

Outcome Measures

Primary Outcome Measures

  1. Describe expectations and beliefs of transgener people about hormonal therapy [12 months]

    qualitative analysis of qualitative data from collective discussions (focus groups)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • being a parent of adolescent/child presenting Gender dysphoria

  • adult subject (age > 18 years) presenting Gender dysphoria

non-inclusion criteria

  • Severe, uncontrolled psychiatric or somatic illness

  • Chronic alcoholism

  • Substance abuse

  • Refusal or linguistic, physical or psychological incapacity to participate in the study

  • Ongoing pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHRU de Nancy Nancy France

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
EVA FEIGERLOVA, Principal investigator, Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT05474768
Other Study ID Numbers:
  • 2021PI221
First Posted:
Jul 26, 2022
Last Update Posted:
Jul 26, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 26, 2022