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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05187442
Other study ID # 20210HS3001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 12, 2022
Est. completion date July 31, 2023

Study information

Verified date August 2023
Source National Taiwan University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Transgender male (TM) is the minority and difficult to reach-up group. Therefore, there is a lack of research on private issues involving TM, such as sex, eroticism, and sexual risk behavior. This study focuses on TM as the research participant, based on Milton Mayeroff's caring theory, to understand the TM's erotic culture and the sexual risks behavior, to evaluate the need for subsequent sexual health care. The research method is a mixed methods research of explanatory design, which recruits participants through purposive sampling and respondent-driven sample (RDS) methods. The first stage is an online questionnaire survey. A total of 321 TMs were recruited. The time of online questionnaire is about 10-15 minutes to get a preliminary understanding of the erotic and sexual risk experience of TM in Taiwan. In the second stage, focus groups and in-depth interviews will be conducted, 2 hours of each group and interview. A total of 29 transgender man and women, and non-binary participants were recruited. The recruitment will be stop when the data are saturated. The analysis of both quantitative and qualitative data can get an in-depth understanding of sex, eroticism, and sexual risk, and violence experiences of the participants. The research results are important for improving the awareness and identification of sexual risk and the assessment of sexual health care needs of TM in health care profession. The results also serve as a reference guide for the development of care needs on sexual health care and anti-violence of transgender people, and for the implement of a gender-friendly environment for medical care.


Recruitment information / eligibility

Status Completed
Enrollment 321
Est. completion date July 31, 2023
Est. primary completion date June 30, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility First stage: Inclusion Criteria: 1. People who used to or currently self-identified as transgender men, regardless of whether they have sex reassignment surgery. 2. Be over 20 years old. 3. Citizen and live in Taiwan. Exclusion Criteria: 1. Not self-identify as transgender men 2. Younger than 20 years old 3. Not citizen and not live in Taiwan. Second stage 1. People who used to or currently self-identified as transgender men, transgender woman or non-binary, regardless of whether they have gender-affirming surgery. 2. Be over 20 years old. 3. Citizen and live in Taiwan. Exclusion Criteria: 1. Not self-identify as transgender men, transgender woman or non-binary. 2. Younger than 20 years old 3. Not citizen and not live in Taiwan.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaire, interview
The first stage is an online questionnaire survey. A total of 321 TMs were recruited. The time of online questionnaire is about 10-15 minutes to get a preliminary understanding of the erotic and sexual risk experience of TM in Taiwan. In the second stage, focus groups and in-depth interviews will be conducted, 2 hours of each group and interview. A total of 29 transgender man and women, and non-binary participants were recruited.

Locations

Country Name City State
Taiwan School of Nursing of National Taiwan University Taipei

Sponsors (2)

Lead Sponsor Collaborator
National Taiwan University Ministry of Science and Technology, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Experience of erotic and sexual risk of transgender men Collect objective data via questionnaires At time of entry into study
Primary Experience of violence experience of transgender Qualitative analysis of interview or focus group. months3-6(In the second stage)
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