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Clinical Trials/ChiCTR1900021042
ChiCTR1900021042
Not yet recruiting
卫生服务研究

跨性別人士的心理健康: 有關介入方式的研究

Nil1 site in 1 country100 target enrollmentStarted: January 1, 1990Last updated:

Overview

Phase
卫生服务研究
Status
Not yet recruiting
Sponsor
Nil
Enrollment
100
Locations
1
Primary Endpoint
Psychological Adjustment (transgender patients only)

Overview

Brief Summary

To investigate the benefits of intervention involving family members of transgender individuals in Hong Kong.

Study Design

Study Type
观察性研究
Primary Purpose
单臂
Masking
N/a

Eligibility Criteria

Ages
18 to — (—)
Sex
All

Inclusion Criteria

  • Experiences symptoms of gender dysphoria;
  • Attends The Gender Identity Disorder Clinic at the Prince of Wales Hospital;
  • 18 Years of age;
  • Patient and the parent both being fluent in Cantonese and/or being literate in Chinese.

Exclusion Criteria

  • Significant intellectual and/or communication deficits

Arms & Interventions

50 patients [+50 of their relevant family member(s)]

Nil

Outcomes

Primary Outcomes

Psychological Adjustment (transgender patients only)

Time Frame: 2 weeks before the intervention, 2 weeks after the intervention, and 1 month after the intervention

Communication Skills (Both family & transgender patients)

Time Frame: 2 weeks before the intervention, 2 weeks after the intervention, and 1 month after the intervention

Transphobic attitude (Family of transgender patients only)

Time Frame: 2 weeks before the intervention, 2 weeks after the intervention, and 1 month after the intervention

Perceived Family Support (transgender patient only)

Time Frame: 2 weeks before the intervention, 2 weeks after the intervention, and 1 month after the intervention

Secondary Outcomes

  • Psychological Adjustment (transgender patients only)(2 weeks before the intervention, 2 weeks after the intervention, and 1 month after the intervention)

Investigators

Sponsor
Nil

Study Sites (1)

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