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Analysis of Depression and Anxiety in Gender Incongruent Patients and Their Associated Factors: A Cross-Sectional Study Based on Multidimensional Clinical, Psychological, and Physiological Characteristics

Analysis of Depression and Anxiety in Gender Incongruent Patients and Their Associated Factors: A Cross-Sectional Study Based on Multidimensional Clinical, Psychological, and Physiological Characteristics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120182
Enrollment
Unknown
Registered
2026-03-10
Start date
2026-03-10
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Gender Incongruence

Interventions

Case group:NA

Sponsors

Beijing Huilongguan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 6 years, no gender restrictions; 2. Meets the diagnostic criteria for gender incongruence according to ICD-11; 3. Does not currently meet the diagnostic criteria for any other mental disorder according to DSM-5, such as depressive disorder, bipolar disorder, schizophrenia, anxiety disorders, post-traumatic stress disorder, etc.; 4. Able to understand and cooperate with the research procedures; 5. Understands and voluntarily participates in this study, with informed consent signed by the participant or their legal guardian.

Exclusion criteria

Exclusion criteria: 1.Based on the investigator's clinical judgment and/or the C-SSRS, the participant has had suicidal ideation with some intent to act within the 6 months prior to screening (i.e., a "Yes" answer to item 4 [active suicidal ideation with some intent to act, without specific plan] or item 5 [active suicidal ideation with specific plan and intent] of the C-SSRS), or has had a history of suicidal behavior within the year prior to screening. 2. Other conditions deemed inappropriate for participation in this study as assessed by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Scale (HAMD-17);Hamilton Anxiety Rating Scale (HAMA);Self-Rating Depression Scale (SDS);Self-Rating Anxiety Scale (SAS);Patient Health Questionnaire-9 (PHQ-9);Generalized Anxiety Disorder Scale (GAD-7);

Secondary

MeasureTime frame
Eysenck Personality Questionaire-Revised ,Short Scale For Chinese (EPQ-RSC));Perceived Social Support Scale (PSSS);Dysfunctional Attitude Scale (DAS);Revision of the Short-form Egna Minnen av Barndoms Uppfostran for Chinese (s-EMBU-C);Parental Psychological Control Scale (PPCS);Defense Style Questionnaire (DSQ);Average Heart Rate;Minimum Heart Rate;Maximum Heart Rate;Follicle-Stimulating Hormone (FSH);Luteinizing Hormone (LH);Estradiol (E2);Testosterone;Progesterone;Prolactin (PRL);

Countries

China

Contacts

Public ContactXiaohong Li/Xinpeng Xu

Beijing Huilongguan Hospital, Capital Medical University

lxhshy2002@163.com+86 158 1040 2994

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026