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Clinical Trials/NCT04160364
NCT04160364
Unknown
Not Applicable

Gender Dysphoria in Children and Adolescents : Parents' Perspectives

Central Hospital, Nancy, France1 site in 1 country20 target enrollmentOctober 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gender Dysphoria
Sponsor
Central Hospital, Nancy, France
Enrollment
20
Locations
1
Primary Endpoint
thematic analysis
Last Updated
5 years ago

Overview

Brief Summary

Gender dysphoria is defined as a persistent incongruence between an experienced gender and the assigned sex at birth Transgender and gender nonconforming persons desire to modify their appearance to be consistent with their self-identified gender identities. In non-binary people, contrary to binary transgender persons, self-identified gender identities do not fit the classical pattern male/female.

During the last decennium, an increase in the number of young subjects, especially children and adolescents, referred to gender identity centres has been observed. A new nosological entity "rapid-onset gender dysphoria in adolescents and young adults" has recently been described in the literature, whose etiology has not been well understood.

This growing demand of adolescents and young adults observed in the recent years is not well understood.

Registry
clinicaltrials.gov
Start Date
October 2020
End Date
January 2021
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Central Hospital, Nancy, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • be a parent of a child \<18 years followed in the endocrinology department of the University Hospital of Nancy for gender dysphoria
  • be in stable couple
  • both parents agree to participate
  • capacity to communicate in French
  • Person who has received complete information on the organization of the research and who agreed to the exploitation of the data

Exclusion Criteria

  • Refusal to participate
  • Inability to be physically, psychologically or linguistically involved in the study

Outcomes

Primary Outcomes

thematic analysis

Time Frame: one year

The recorde material will be coded using descriptive codes. Conceptual notes will be written, through processes of condensation, comparison and abstracting the initial notes. Connections between notes will be noted and synthesized, and emergent themes will be developed.

Study Sites (1)

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