Different Education Methods and Self Vulvar Examination (SVE) (SVE)

March 14, 2026 updated by: Yeditepe University

Comparison of the Effects of Different Education Methods on Vulva Self-Examination on the Knowledge and Behaviors of University Students About Self Vulvar Examination: A Randomized Controlled Trial

The goal of this clinical trial is to increase students' awareness about Self-Vulvar Examination (SVE), and to evaluate the effect of a peer education module and an educational brochure on students' knowledge and behaviors related to SVE.

The main questions it aims to answer are:

  • Does providing peer education module and an educational brochure about SVE increase students' knowledge levels regarding SVE?
  • Does providing peer education module and an educational brochure about SVE increase students' behaviors of practice SVE? Researchers will compare the peer education module and educational brochure regarding KKVM with a control group to determine whether it has an impact on students' knowledge and behavior about KKVM.

Students; After the pretest, they will learn about KKVM through a peer education module or educational brochure, or they will be in the control group.

Three months later, a posttest will assess their knowledge and behaviors about KKVM.

Study Overview

Detailed Description

Providing self vulvar examination (VSE) education to women enables them to take an active role in monitoring their own health, facilitates the early detection of potential abnormalities, and ensures timely intervention and management. Furthermore, providing VSE education to women at a young age plays a critical role in developing early awareness and establishing VSE, which is a protective health behavior, as a habit. In recent years, one of the methods used within the scope of health education is the 'peer education model,' which is one of the 'models centered on social interaction,' where students work in a way that supports each other's learning. Therefore, this study aims to determine the effect of peer education and an educational brochure about VSE on the knowledge and behaviors of university students regarding VSE The sample of the research; It is planned to consist of a total of 105 student, 35 in the Peer Education Group, 35 in the Brochure Group and 35 in the Control Group, who meet the inclusion criteria and voluntarily agreed to participate in the research.

During the pre-test and post-test data collection phase, it is planned to use, 'Personal Information Form', 'Vulva Health and SVE Information Form', 'SVE Behavior Determination Form', SVE Behavior Determination, Education Brochure Satisfaction Determination Form', 'Peer Education Module Satisfaction Determination Form' and 'SVE Behavior Determination Form'.

Intervention 1 (Brochure Group) consists of second-year nursing students. A brochure prepared about VSE will be distributed to this group. Before the brochure is distributed, a pre-test, consisting of the Personal Information Form and the Vulvar Health and VSE Knowledge Form, will be administered. After the form pretest, the brochures will be distributed, and a 3-month follow-up will be conducted. At the end of the 3-month period, the VSE Knowledge Form and the VSE Behavior and Satisfaction with the Educational Brochure Form will be administered to the second-year students as a post-test. In the Intervention 2 (Peer Education Group) module, first-year nursing students will be provided with a 35-minute presentation on Vulvar Health and VSE (Vulvar Self-Examination). Following the training, the 'Satisfaction with the Peer Education Module Form' will be administered to the students. The Intervention 2 group will also have a 3-month follow-up period. At the end of the 3 months, the 'Vulvar Health and VSE Knowledge Form' and the 'VSE Behavior Determination Form' will be transmitted online as a post-test, and the post-test data will be collected. Preparatory students will be randomly assigned to the control group. The Personal Information Form and the Vulvar Health and VSE (Vulvar Self-Examination) Knowledge Form will be administered online to these students as a pre-test. As a post-test, the Vulvar Health and VSE Knowledge Form and the VSE Behavior Determination Form will be administered online at the end of the 3-month follow-up period.

Study Type

Interventional

Enrollment (Actual)

105

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • • Being a female student in the Yeditepe University Faculty of Health Sciences, Department of Nursing

    • Not having had a previous vulvar mass or cancer
    • Not having any communication barriers
    • Being able to read and understand Turkish
    • Having a mobile phone with internet access.

Exclusion Criteria:

  • • Not being a female student in the Yeditepe University Faculty of Health Sciences Nursing Department

    • Having previously had a vulvar mass or cancer
    • Having any communication barriers
    • Not being able to read or understand Turkish
    • Not having a mobile phone with internet access

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention 1 ( Brochure Group)
It consists of second-year nursing students. A brochure prepared about VSE (Vulvar Self-Examination) will be distributed to this group. Before the brochure is distributed, a pre-test, consisting of the Personal Information Form and the Vulvar Health and VSE Knowledge Form, will be administered. After the form application, the brochures will be distributed, and a 3-month follow-up will be conducted. At the end of the 3-month period, the VSE Knowledge Form and the VSE Behavior and Satisfaction with the Educational Brochure Form will be administered to the second-year students as a post-test.
A brochure about the Vulvar Self-Examination (VSE) will be distributed to this group, and a three-month follow-up will be conducted. At the end of the three-month period, a posttest will be administered to second-year students to measure changes in knowledge and behavior.
Experimental: Intervention 2 (Peer Education Group)
In the peer education module, first-year nursing students will be provided with a 35-minute presentation, which we prepared, on Vulvar Health and VSE (Vulvar Self-Examination). Following the training, the 'Satisfaction with the Peer Education Module Form' will be administered to the students. The Intervention 2 group will also have a 3-month follow-up period. At the end of the 3 months, the 'Vulvar Health and VSE Knowledge Form' and the 'VSE Behavior Determination Form' will be transmitted online as a post-test, and the post-test data will be collected.
Following the peer education, students will also have a 3-month follow-up period. At the end of the 3 months, the post-test data will be collected o measure changes in knowledge and behavior.
Active Comparator: Control Group
Preparatory students were randomly selected as the control group. The pre-tests were sent to the preparatory students online. As a post-test, the 'Vulvar Health and VSE (Vulvar Self-Examination) Knowledge Form' and the 'VSE Behavior Determination Form' will be administered online at the end of the 3-month follow-up period.
The pre-tests were sent to the control group. As a post-test, will be administered online at the end of the 3-month follow-up period.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
VSE Behavior Determination Form
Time Frame: Baseline, 3 months post-intervention
This form consists of two questions prepared to determine the students' VSE (Vulvar Self-Examination) practices and their reasons for not performing it."
Baseline, 3 months post-intervention
Vulvar Health and VSE Knowledge Form
Time Frame: Baseline, 3 months post-intervention
This form contains 16 questions aimed at determining the students' knowledge about vulvar health.
Baseline, 3 months post-intervention

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
VSE Behavior and Satisfaction with the Educational Brochure Form
Time Frame: 3 months post-intervention
This form consists of two questions aimed at assessing the students' satisfaction with the educational method used. Participants were asked to indicate their level of satisfaction with the brochure by marking on a Visual Analog Scale (VAS).
3 months post-intervention
Satisfaction with the Peer Education Module Form
Time Frame: 3 months post-intervention
This form consists of three questions aimed at assessing the students' satisfaction with the educational method used. Participants were asked to indicate their level of satisfaction with the peer education by marking on a Visual Analog Scale (VAS).
3 months post-intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2023

Primary Completion (Actual)

January 30, 2026

Study Completion (Estimated)

June 30, 2026

Study Registration Dates

First Submitted

November 17, 2025

First Submitted That Met QC Criteria

March 14, 2026

First Posted (Actual)

March 18, 2026

Study Record Updates

Last Update Posted (Actual)

March 18, 2026

Last Update Submitted That Met QC Criteria

March 14, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Health Knowledge,Practices,Attitudes

Clinical Trials on Brochure

Subscribe