NCT07110909

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
103

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 2, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 28, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

August 8, 2025

Completed
Last Updated

August 8, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

July 28, 2025

Last Update Submit

August 1, 2025

Conditions

Keywords

HPVeducationknowledge levelawarenessmidwife

Outcome Measures

Primary Outcomes (1)

  • HPV Knowledge Increase

    The increase in women's knowledge about HPV is measured using an HPV knowledge questionnaire. The questionnaire is scored from 0 to 20 points, with higher scores indicating greater knowledge.

    1 week

Secondary Outcomes (1)

  • Increasing HPV awareness among women

    1 week

Study Arms (2)

No HPV Education

NO INTERVENTION

Control group without HPV education.

Experimental

EXPERIMENTAL

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

Other: HPV Education

Interventions

HPV Education

Experimental

Eligibility Criteria

Age18 Years - 49 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsWomen
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Tokat Gaziosmanpaşa University Rectorate General Secretariat Taşlıçiftlik Campus, 60250 Tokat/Central

Tokat Province, Center, 60250, Turkey (Türkiye)

Location

Study Officials

  • GİZEM ÇITAK, Asist. Prof

    Tokat Gaziosmanpaşa University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: experimental group: 50; control group: 53
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

July 28, 2025

First Posted

August 8, 2025

Study Start

January 1, 2025

Primary Completion

April 1, 2025

Study Completion

April 2, 2025

Last Updated

August 8, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

The IPD will not be shared because the data include sensitive health information and participants did not consent to data sharing.

Locations