Evaluating Sexual Functioning in Trans Men During the Gender Affirmation Process: A Mixed Methods Study

NCT ID: NCT07131267

Last Updated: 2025-08-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

52 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-08-05

Study Completion Date

2026-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Both sexual experiences and the process of gender transition initiated to reduce gender dysphoria carry cultural characteristics. Gender categories, societal expectations for each gender, and attitudes toward sexual minorities in a given society can shape the lived experiences of trans individuals. Therefore, research on individuals with gender dysphoria in different cultural contexts is of great importance. To our knowledge, no study in Türkiye has examined sexual functioning in trans individuals undergoing gender transition. For this reason, our study aimed to investigate how sexual functioning is affected by the gender transition process in trans men with gender dysphoria, using both quantitative and qualitative methods.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

For the quantitative part of the study, 52 participants will receive a sociodemographic and clinical data form, Arizona Sexual Experiences Scale, Sexual Desire Inventory, Utrecht Gender Dysphoria Scale, Depression Anxiety Stress Scale-21, and WHOQOL-100 sexual quality of life subscale.

While performing a qualitative study, 12 participants will receive questions about their sexual functioning during the gender affirmation process.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Sexual Functioning Transgender Men Gender Affirmation Surgery

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Study group

Trans men during the gender affirmation process

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

18 years or older Diagnosed with gender dysphoria by two different physicians Getting medical support for the gender affirmation process

Exclusion Criteria

Over 65 years Diagnosed with intellectual disability, dementia, or organic mental disorders Having a systemic disease that negatively impacts sexual function Getting a score above 3 on the Clinical Global Impression Scale
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Eskisehir Osmangazi University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Imran Gokcen Yilmaz-Karaman

Associate professor doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Imran G Yilmaz-Karaman, Assoc.Prof.

Role: STUDY_DIRECTOR

Eskişehir Osmangazi University, Faculty of Medicine

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Eskişehir Osmangazi University, Faculty of Medicine, Department of Psychiatry

Eskişehir, Türkiye, Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Imran G Yilmaz-Karaman, Assoc.Prof.

Role: CONTACT

02222392979 ext. 3600

Aylin Aydin, Assist.Dr.

Role: CONTACT

02222392979 ext. 3600

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Imran G Yilmaz-Karaman, Assoc.Prof.

Role: primary

00902222392979 ext. 3604

Aylin Aydin, Assisst.Dr.

Role: backup

00902222392979 ext. 3600

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

EskisehirOU 28.05.2025/26

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.