Effıcıency of Sexual and Reproductıve Health Educatıon
Evaluatıon of The Effıcıency of Sexual and Reproductıve Health Educatıon
1 other identifier
interventional
165
1 country
1
Brief Summary
The youth period is a period when information and education are important. Reproductive and sexual health problems have an important place in aging health problems in youth (Gölbaşlı 2003). All over the world, STIs are most common in the 20-24 age group, followed by the 15-19 and 25-29 age groups. STIs are the most common disease in many countries, especially among young people between the ages of 15-29 (Topbaş et al. 2003). STIs, which are one of the factors that negatively affect public health; are infections transmitted from person to person through sexual contact. According to WHO estimates, approximately 350 million people suffer from curable STIs each year, and the incidence and prevalence of STIs among young people in developed and developing countries are increasing. Although young adults are generally at risk, STIs are most common in people aged 15-49. They have a very important place in terms of human health because they are frequently seen, difficult to diagnose, and cause serious complications when not treated. Incomplete and incorrect information among people who start sexual intercourse at an early age causes difficulties in the prevention of these diseases (Özalp et al. 2012). Having sexual intercourse at an early age, being polygamous, having special sexual preferences, being with or having sex with those who have paid for sexual intercourse, and not using condoms are among the risk factors for STIs (Siyez 2009). We can say that the age period in which STIs are common is parallel to sexual activity. In addition to various socio-demographic factors, it is likely that the most provoking issue in this period is the lack of knowledge of young people (Karaköse and Aydın 2011). In the STD guide published by the CDC, it is recommended to evaluate the people who constitute the risk group in the prevention of these diseases and to provide education and counseling (CDC, 2020). In this context, training to increase the level of knowledge and awareness of young people, who are one of the high-risk groups in society in terms of STD, is important in terms of reducing risky sexual behaviors, early diagnosis, and treatment. Based on all these reasons; It is aimed to evaluate the effectiveness of sexual and reproductive health education given to university students.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 15, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2022
CompletedFirst Submitted
Initial submission to the registry
May 9, 2023
CompletedFirst Posted
Study publicly available on registry
May 18, 2023
CompletedMay 18, 2023
May 1, 2023
5 months
May 9, 2023
May 9, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Participant Identification Form Diagnostic Form
The participant identification form, which includes the introductory characteristics of the students, was prepared by the researchers in line with the literature (Altay et al., 2020; Vongxay et al., 2019). The form includes students' socio-demographic characteristics, their status of obtaining information about SRH and sources of information, their experiences with SRH and their thoughts on sexual intercourse. The form consists of 28 questions in total.
5 Months
Secondary Outcomes (1)
Sexual Health Knowledge Test
5 Months
Other Outcomes (1)
Reproductive Health Scale for Turkish Adolescents
5 Months
Study Arms (3)
Face-to-face Training Group
EXPERIMENTALStudents in this group will be given face-to-face training on SRH by the principal researcher accompanied by PowerPoint.
DataMatrix supported Face-to-face training group
EXPERIMENTALBefore starting the training, a QR code including PowerPoint on SRH will be given to the students in the group that receives training with QR code support (on the first slide). Students will be directed to the URL automatically determined by the researcher by scanning the QR code with the camera of their smartphones. Students will follow the lesson with the QR code given simultaneously with the training given during the education process.
Online training group
EXPERIMENTALThe students in the online training group will be given training on SRH/RES on an online platform accompanied by PowerPoint by the principal researcher.
Interventions
The training will take approximately 3 hours. The training will be done interactively, allowing students to talk to each other and ask questions, and will end with 10 minutes of time for students' questions.
Students will follow the lesson with the QR code given simultaneously with the training given during the education process. The training will be held in such a way that the students will be given the opportunity to ask questions and will end with 10 minutes of time to be given to the questions of the students.
The training will take approximately 3 hours. The training will be done interactively, allowing students to talk to each other and ask questions, and will end with 10 minutes of time for students' questions.
Eligibility Criteria
You may qualify if:
- Volunteering to participate in the research,
- Have not taken Sexual Health, Infectious Diseases course before
- Students without communication barriers will be included.
You may not qualify if:
- Incorrect or incomplete form filling
- The participant's wish to withdraw from the study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Marmara University
Istanbul, 34500, Turkey (Türkiye)
Related Links
Study Officials
- PRINCIPAL INVESTIGATOR
Tuğba Öz
ev
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD RN, Professor
Study Record Dates
First Submitted
May 9, 2023
First Posted
May 18, 2023
Study Start
May 15, 2022
Primary Completion
September 30, 2022
Study Completion
December 30, 2022
Last Updated
May 18, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will not share