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Recruiting NCT05927350

Research Participation With Transgender and Gender-Diverse Youth

— Observational Transgender Persons

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Survey.
Who it may be relevant to
Registry conditions: Transgender Persons. Basic parameters: 15 years — 21 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Research has historically excluded the participation of transgender and gender-diverse people. The purpose of this research study is to find out about what goes into a transgender and gender-diverse youth's decision to participate in research. The results of this study will be used to improve access to research for transgender and gender-diverse youth and therefore, improve the representation of transgender and gender-diverse youth as research participants in research.

Interventions

  • Other Survey
    Survey asking about sociodemographics, pediatric research participation, experience with research, gender minority stress and resilience, vaccine hesitancy, medical mistrust, and connectedness to the LGBT community

Primary outcome measures

  • Quantitative Assessment of Pediatric Research Participation in Transgender Youth [Time frame: through study completion, estimated to be 3 months]
  • Qualitative Assessment of Pediatric Research Participation in Transgender Youth [Time frame: through study completion, estimated to be 3 months]

Eligibility criteria

Inclusion criteria

  • Gender identity different then sex assigned at birth
  • Between the ages 15-21 years

Exclusion criteria

  • Gender identity the same as their sex assigned at birth
  • Younger than 15 years of age, and older than 21 years of age

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Virginia Commonwealth University — Richmond

Identifiers

NCT: NCT05927350 · HM20026635

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗