The Effect of a Transtheoretical Model-Based Educational Intervention on First-Year Nursing Students' HPV Knowledge, Health Beliefs, and Vaccination Behavior Intentions
Condition(s) studied
Investigational drug(s) / intervention(s)
TTM-Based Educational Program: A structured, stage-matched educational intervention based on the Transtheoretical Model, delivered face-to-face in five modules aligned with Precontemplation, Contemplation, Preparation, Action, and Maintenance stage
Study summary
The purpose of this study is to examine the impact of a structured educational program based on the Transtheoretical Model (TTM) on HPV knowledge, health beliefs, and vaccination behavioral intentions among first-year nursing students. The study will also evaluate how the intervention affects students' HPV vaccine readiness compared to the TTM.
The primary questions addressed by the study are:
* Does the TTM-based educational intervention increase students' knowledge about HPV and the HPV vaccine?
* Does the program change students' health beliefs regarding susceptibility, severity, benefits, and barriers to HPV and the HPV vaccine?
* Does the program improve students' intentions and readiness to receive the HPV vaccine?
* Do students move to a higher behavioral readiness stage (from Precontemplation to Contemplation, Preparation, Action, or Maintenance) after the intervention?
The researcher will compare the TTM-based educational intervention with a control group that did not receive structured education to determine whether a personalized, stage-based approach is more effective in improving HPV-related outcomes among nursing students.
Participants will:
* Complete baseline questionnaires measuring HPV knowledge, health beliefs, and vaccination intention.
* The experimental group (intervention group) will receive personalized TTM-based education, face-to-face instruction in modules aligned with the five TTM phases (Precontemplation, Contemplation, Preparation, Action, and Maintenance).
* The experimental group will participate in educational sessions designed to raise awareness, correct misinformation, support decision-making, and encourage protective behaviors.
* The control group will not receive any educational program.
* All participants in the experimental and control groups will complete the same questionnaires again to assess changes after the intervention.
The TTM-based educational intervention provides:
* Staged counseling
* Information about HPV and the HPV vaccine
* Activities to raise awareness, strengthen motivation, and support vaccination adoption
* Personalized feedback based on student readiness
* Structured modules focusing on knowledge, belief, and behavior change strategies
The study population included first-year nursing students enrolled in the Faculty of Health Sciences. A total of 88 participants will be recruited and randomly assigned to either the intervention (n=44) or control (n=44) groups through simple randomization.
The results of this study are expected to contribute to the development of evidence-based education strategies in nursing, support of behavioral change models in health education, and strengthen the role of future nurses in HPV prevention, vaccine advocacy, and public health practice.
Eligibility
Primary outcome measure(s)
- Vaccination Behavior Intention Scale — Baseline and after completion of the 10-week intervention (5 sessions delivered every 2 weeks)
Behavioral intention to receive the HPV vaccine will be assessed using the HPV Vaccination Intention Scale, a 6-item instrument developed based on the Theory of Planned Behavior. The scale evaluates participants' intention to receive the HPV vaccine, with higher scores indicating stronger intention to be vaccinated. The secondary outcome is the change in intention score from baseline to post-intervention.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| Faculty of Health Sciences | Adana | CUKUROVA | Not Yet Recruiting |
| Cukurova University | Adana | Turkey (Türkiye) | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07248904 on ClinicalTrials.gov ↗ ← All trials in Turkey