The Effect of HPV Education Provided to Women on Their Knowledge Levels, HPV Screening, and Vaccination Uptake
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-35
SponsorUfuk University
About this trial
Type of Study: This study was planned to be an observational study.
Purpose of the Study: To evaluate the impact of HPV education given to women on their knowledge levels and HPV screening and vaccination.The main question\[s\] it aims to answer \[is/are\]:
H1: There is a difference in the mean Human Papillomavirus (HPV) Knowledge Scale score between the intervention group women who participated in Human Papillomavirus (HPV) education and the control group women.
H2: There is a difference between the intervention group women and the control group women in terms of their participation in HPV screening tests.
H2: There is a difference between the intervention group women and the control group women in terms of their HPV vaccination status.
Participants Participants will be assigned to a control and intervention group. Online training will be provided to the intervention group, and the results of the training will be reported.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Being female
Women aged 18-35 years
Ability to speak and understand Turkish at a level sufficient to communicate with the researcher
Having the technical equipment necessary to participate in a video interview
Disqualifiers
Being male
Having severe physical or cognitive impairments that prevent completing the questionnaire
Being under 18 years of age or over 35 years of age
Inability to speak or understand Turkish
Trial design
Design model
Single group
Treatments tested in this trial
Online Education Intervention Group
BehavioralAn online training session will be scheduled for the intervention group. The training will consist of two 40-minute session. After the online training, the training materials will be shared with the group. One week after the training, an informational brochure prepared on the topic will be sent to the intervention group via WhatsApp as a reminder, and any questions they may have will be answered. Two weeks after delivering the brochure, the questionnaire/scale forms will be administered to both groups as the first follow-up. Eight weeks after the first follow-up, the same forms will be administered again as the post-test. The WhatsApp group will remain open and interaction will be allowed throughout the research period.
Contral Group
Other interventionNo intervention will be applied to the control group. Following the completion of the study, the brochure prepared on the topic will be sent to them via WhatsApp.
Treatment groups
64 Participants
are divided into 1 treatment groupGroup A: Online Education Intervention GroupExperimental treatment 2 interventions
Trial outcomes
Primary outcomes
1
Change in HPV Knowledge Score
Change in participants' HPV Knowledge Scale scores measured at baseline, first follow-up, and final follow-up. The measure evaluates the effect of the online education and brochure intervention compared to the control group.
Time frame
Baseline (before intervention), 2 weeks after brochure delivery (first follow-up), and 8 weeks after the first follow-up (final follow-up)Secondary outcomes
1
Sustained HPV Knowledge Score (Knowledge Retention)
Final follow-up (8 weeks after the first follow-up)
Time frame
Knowledge retention will be assessed by comparing HPV Knowledge Scale scores between groups at the final follow-up. Higher scores indicate better long-term retention of information provided by the intervention.Sponsors and contacts
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Source ClinicalTrials.gov