NCT07007975

Brief Summary

There are cross-sectional or quasi-experimental studies in the literature on gynecological cancer awareness, but there are no fully experimental studies. The study we will conduct will use a control group and will be a fully experimental study. Thus, it is thought to contribute more to the field. The purpose of the study is to determine the effect of gynecological cancer education given to married women on their gynecological cancer awareness and healthy living behaviors.

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2025

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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

First Submitted

Initial submission to the registry

May 25, 2025

Completed
5 days until next milestone

Study Start

First participant enrolled

May 30, 2025

Completed
6 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 5, 2025

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 6, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 7, 2025

Completed
Last Updated

June 6, 2025

Status Verified

December 1, 2024

Enrollment Period

6 days

First QC Date

May 25, 2025

Last Update Submit

June 3, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Gynecological cancer awareness scale

    Preliminary test results received. The minimum score that can be obtained from the scale is 41, the maximum score is 205. The pre-training scale score average of the experimental group is 90.97.

    4 weeks

Study Arms (2)

Web based training

EXPERIMENTAL

Web-based training will be given to experimental group and the results of the training will be evaluated

Behavioral: Web based training

control group

NO INTERVENTION

Participants in this group will not be provided with training

Interventions

This group will receive information about healthy lifestyle behaviors and gynecological cancer awareness.

Web based training

Eligibility Criteria

Age20 Years - 65 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility DetailsOnly women participated
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Being between the ages of 20-65
  • Being open to communication
  • Being literate
  • Being able to use the internet
  • Having a smart phone or computer

You may not qualify if:

  • Being pregnant
  • Being breastfeeding
  • Not being able to use a website
  • Not having watched all the videos on the website
  • Having a history of gynecological cancer in oneself or in one's family

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Family Health Center

Malatya, 44000, Turkey (Türkiye)

Location

Study Officials

  • Yurdagül Y Yağmur

    Inonu University

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD Student

Study Record Dates

First Submitted

May 25, 2025

First Posted

June 6, 2025

Study Start

May 30, 2025

Primary Completion

June 5, 2025

Study Completion

June 7, 2025

Last Updated

June 6, 2025

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will share

Scale results will be shared.

Shared Documents
SAP
Time Frame
It will be accessible in March 2025. It will be accessible for 6 months.
Access Criteria
Those working in the field of nursing will be able to access it.

Locations