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Not yet recruiting NCT07022392

Feasibility and Acceptability of the Technology Based Enhanced Gender Support Platform Implementation With Parents

No phase Interventional Parents Usability

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: Technology-enhanced gender support platform.
Who it may be relevant to
Registry conditions: Parents, Usability. Basic parameters: from 18 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 →

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Official title

Feasibility and Acceptability of the Technology Based Enhanced Gender Support Platform Implementation

Overview

This is a small pilot feasibility and acceptability study of implementing a Technology-Enhanced Gender Support (TEGS) platform with parents and caregivers. Parents and caregivers who consent to participate will complete an electronic survey at baseline. They will then receive access to the TEGS platform and complete follow up surveys 1 mo and 3 mo after. Each participant will also be given the option to participate in an exit interview.

Interventions

  • Other Technology-enhanced gender support platform
    Technology-based platform to support parents

Primary outcome measures

  • System Usability Scale [Time frame: 1 month and 3 months]
Secondary outcome measures (1)
  • Transgender Family Acceptance To Empowerment scale [Time frame: Baseline, 1 month, 3 month]

Eligibility criteria

Inclusion criteria

  • Parent of a gender diverse youth aged 8-17
  • Has access to the internet
  • Can speak or read English

Exclusion criteria

  • Not a parent of a gender diverse youth aged 8-17
  • No access to the internet
  • Cannot speak or read in English

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

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Health services research

Study locations

United States · 1 center
  • Seattle Children's Hospital — Seattle

Identifiers

NCT: NCT07022392 · STUDY00005068 · K08HS029028-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗