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Gender Dysphoria in Children and Adolescents : Parents' Perspectives

Gender Dysphoria in Children and Adolescents : Parents' Perspectives

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04160364
Acronym
GeDyPar
Enrollment
20
Registered
2019-11-13
Start date
2020-10-31
Completion date
2021-01-31
Last updated
2020-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gender Dysphoria

Keywords

children, adolescents, parents

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.

Interventions

qualitative research via guided interview

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
thematic analysisone yearThe 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.

Countries

France

Contacts

Primary ContactEva Feigerlova, MD, PhD
e.feigerlova@chru-nancy.Fr00330383153412

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026