Impact of HPV Education on Knowledge, Awareness, and Concern

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

103 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-01

Study Completion Date

2025-04-02

Brief Summary

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This randomized controlled study is being conducted between January and April 2025 at a Family Health Center in the Black Sea Region with 103 women (intervention group: 50, control group: 53) selected via randomizer.org. Participants complete pre-tests, receive HPV and cervical cancer prevention education, and take post-tests to evaluate the impact of the intervention.

Keywords: HPV, education, knowledge, awareness, midwife.

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Detailed Description

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This study is designed as a randomized controlled trial aimed at evaluating the impact of educational interventions on HPV awareness, knowledge levels, and concerns among women. The research is being carried out at a Family Health Center in the Black Sea Region between January and April 2025. A total of 103 women have been selected through randomizer.org and assigned to either the intervention group (n=50) or control group (n=53).

Participants are initially assessed using a Personal Information Form, the HPV Knowledge Scale, and the HPV Awareness and Concern Scale. The intervention group receives structured education on HPV and cervical cancer prevention delivered by midwives and healthcare professionals. Post-tests are planned to assess potential changes in the measured variables. The study emphasizes the importance of healthcare-based education in improving public awareness and preventive health behaviors.

Keywords: HPV, education, knowledge, awareness, prevention, midwife, cervical cancer.

Conditions

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Human Papilloma Virus (HPV)

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

experimental group: 50; control group: 53

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Participants

Study Groups

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No HPV Education

Control group without HPV education.

Group Type NO_INTERVENTION

No interventions assigned to this group

Experimental

Participants received HPV education to increase awareness and prevention of cervical cancer

Group Type EXPERIMENTAL

HPV Education

Intervention Type OTHER

HPV Education

Interventions

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HPV Education

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being a woman aged 18-49
* Not having received any previous education about HPV
* Volunteering to participate in the study and providing written consent

Exclusion Criteria

* Having been diagnosed with HPV or being in treatment
* Having previously received information or counselling about HPV
* Refusing or withdrawing from the education and data collection process

Minimum Eligible Age

18 Years

Maximum Eligible Age

49 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No