Yeditepe University
Istanbul, Turkey (Türkiye)
NCT Number: NCT07479459
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.
This study is active but is not currently recruiting participants.
Female
Interventional
Not applicable
Istanbul, Turkey (Türkiye)
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
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.
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.
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."
Time frame: Baseline, 3 months post-intervention
This form contains 16 questions aimed at determining the students' knowledge about vulvar health.
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).
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).
Yeditepe University
Other
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
Acronym: SVE
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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