The Effect of Gender Education Provided to Health Sciences Students on Gender Perception and Roles
NCT ID: NCT07041346
Last Updated: 2025-06-27
Study Results
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.
ACTIVE_NOT_RECRUITING
NA
70 participants
INTERVENTIONAL
2025-06-19
2025-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
In this context, sexual health education plays a vital role in raising awareness about societal norms and helping transform these norms. Gender inequality is another major barrier that complicates the accurate understanding of sexual health. In many communities, especially for women, sexual rights are limited due to cultural values, traditional beliefs, and social pressures. This restricts their access to sexual health services and their ability to protect themselves.
Sexual health education aims to eliminate these inequalities and ensure that all individuals, regardless of gender, can maintain a healthy sexual life with equal rights. These educational efforts not only create awareness about gender inequality but also support the promotion of healthy and safe sexual behaviors.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Gender Microagression Psychoeducation
NCT07120360
Young Women on Sexual and Reproductive Health Knowledge and Stigma Levels
NCT05770804
Sexual Health Education Given to Women
NCT07037602
Flipped Classroom Sexual Health Education Trial
NCT07306208
Sexual Function and Quality of Sexual Life in Women With Physical Disabilities
NCT07042646
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Participants will be informed that no financial compensation will be provided for participation, and this will be clearly stated in the written informed consent form.
Following the approval of the ethics committee, institutional permission will be obtained from Istanbul Aydın University, where the study will be conducted. The study will take place at the Faculty of Health Sciences, where one of the researchers, Beyzanur İşbay Aydemir, is affiliated.
Students enrolled in various departments (e.g., Nursing, Physiotherapy and Rehabilitation, Audiology) within the Faculty of Health Sciences who voluntarily agree to participate will be included in the study.
Data will be collected using a Diagnostic Form, the Gender Perception Scale, and the Attitude Scale Towards Gender Roles. Participants who agree to join the study will be fully informed by the researcher about the purpose, scope, and procedures of the research. After this briefing, both verbal and written informed consent will be obtained, and the forms will be completed.
To inform and invite students to the study, a research announcement poster will be prepared and displayed on bulletin boards throughout the Faculty of Health Sciences campus.
In addition, faculty members teaching in relevant departments will be asked to provide a brief explanation of the study during class and to encourage student participation. This strategy aims to increase awareness of the study and reach a broader group of students.
The research will utilize a pre-test-post-test control group experimental design. Students who provide informed consent and meet the inclusion criteria will be randomly assigned to the experimental and control groups using the simple randomization method.
This random assignment will be conducted using computer-based software (e.g., randomizer.org), ensuring an unbiased and balanced distribution across the study groups.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Experimental
Education
1. Objectives of the Training Program To increase students' knowledge and awareness of gender concepts, gender roles, and gender inequality.
To help students develop more conscious and critical thinking skills regarding social norms and gender-based discrimination.
To promote the development of gender-sensitive attitudes and contribute to positive attitude changes following the training.
2. Duration and Structure of the Training Total Duration: 2 weeks
Weekly Duration: 2 hours
Training Format: In-person
Training Methods: Presentations, group discussions, surveys, brainstorming, Q\&A sessions, debates
3. Training Content and Modules Week 1 Topic 1: Fundamental Concepts, Gender Roles, and Inequality
Introduction and Training Objectives
Gender and Social Norms: Definition of gender norms and their impact on individuals
No Intervention
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Education
1. Objectives of the Training Program To increase students' knowledge and awareness of gender concepts, gender roles, and gender inequality.
To help students develop more conscious and critical thinking skills regarding social norms and gender-based discrimination.
To promote the development of gender-sensitive attitudes and contribute to positive attitude changes following the training.
2. Duration and Structure of the Training Total Duration: 2 weeks
Weekly Duration: 2 hours
Training Format: In-person
Training Methods: Presentations, group discussions, surveys, brainstorming, Q\&A sessions, debates
3. Training Content and Modules Week 1 Topic 1: Fundamental Concepts, Gender Roles, and Inequality
Introduction and Training Objectives
Gender and Social Norms: Definition of gender norms and their impact on individuals
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Being 18 years of age or older
Voluntarily agreeing to participate in the study
Exclusion Criteria
18 Years
45 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Saglik Bilimleri Universitesi
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Beyzanur İşbay Aydemir
Lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sağlık Bilimleri Ünversitesi
Istanbul, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2025/07
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.