Clinical trial Recruiting at 1 site Observational Ages 18 to 65

Gender differences in depression symptoms, resilience, and stigma among adults with major depression

Official title: A Comparative Examination of Depression Severity, Gender-Sensitive Depressive Symptoms, Psychological Resilience, and Stigma Levels in Women and Men With Major Depressive Disorder

Run by Eskisehir Osmangazi University · NCT07474363 · Data updated 2026-11-12

This project will look to see if men and women with major depressive disorder show different symptom patterns, resilience levels, and experiences of self and social stigma.

Quick facts

Study typeObservational
Ages18 Years to 65 Years
SexAll
Enrollment90 (estimated)
SponsorEskisehir Osmangazi University
Academic / other
Locations1 site (Eskişehir, Eskişehir)
StatusRecruiting
StartedJune 1, 2025
Main results expectedApril 2026
Study endsNovember 2026
Registry record updatedMarch 25, 2026
Trial IDNCT07474363 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 to 65 with a current DSM-5 diagnosis of Major Depressive Disorder who can provide informed consent and attend the outpatient clinic are ideal candidates.

Probably not a fit

People with intellectual disability, severe neurological disorders, other comorbid psychiatric diagnoses, depression caused by a medical condition or substance use, or those outside the 18–65 age range will not be eligible and are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational, cross-sectional study of adults aged 18–65 diagnosed with Major Depressive Disorder at the Psychiatry Outpatient Clinic of Eskişehir Osmangazi University. Participants who consent will complete clinical interviews and standardized questionnaires measuring depression severity, gender-sensitive symptom profiles, psychological resilience, self-stigma, and perceived social stigma. People with intellectual disability, severe neurological disorders, other psychiatric comorbidities, or depression secondary to medical conditions or substance use are excluded. The data will be analyzed to compare symptom expression and stigma/resilience patterns between male and female participants and explore relationships between these factors.

Why it matters

Potential benefit: If successful, the findings could help clinicians recognize gender-specific symptom patterns and stigma-related barriers so care and outreach can be better tailored.

How similar studies have gone: Previous research has documented gender differences in depressive symptom expression and stigma, though combining detailed gender-sensitive symptom profiling with resilience and stigma measures in a single outpatient sample is less common.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Male and female patients aged 18 to 65 years
* Diagnosis of Major Depressive Disorder according to DSM-5 at the time of study participation
* Provision of voluntary informed consent

Exclusion Criteria:

* Intellectual disability
* Severe neurological disorders
* Comorbid psychiatric diagnoses
* Depressive disorder secondary to an organic medical condition
* Depressive disorder secondary to substance use

Where it's running

  • the Department of Psychiatry Outpatient Clinic at Eskişehir Osmangazi University Faculty of Medicine
    Eskişehir, Eskişehir, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.