Effect of Web-based Nursing Navigator Programme on Breast Cancer Screening Behaviors in Women at High Risk of Breast Cancer
WeT-HNP
1 other identifier
interventional
104
1 country
2
Brief Summary
The aim of this project is to determine the effect of the Web-Based Nurse Navigation Program on breast cancer screening behaviors (mammography, BSE, CBE) in women at high risk of breast cancer. The program to be developed within the scope of the project is named as "Web-Based Nurse Navigation Program (WeT-HNP)", which reflects the web-based and navigation concepts.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Feb 2026
Shorter than P25 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 3, 2025
CompletedFirst Posted
Study publicly available on registry
June 11, 2025
CompletedStudy Start
First participant enrolled
February 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2026
ExpectedMay 1, 2026
July 1, 2025
3 months
June 3, 2025
April 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
mammography rates
browsing behavior monitoring form
baseline, 6 months
rate of breast self-examination
screening behaviors follow-up form
baseline, 3 months
rate of clinical breast examination
screening behaviors follow-up form
baseline, 6 months
Secondary Outcomes (3)
Health perceptions
baseline, 6 months
Breast cancer fear score
baseline, 6 months
perception of mammography competence
baseline, 6 months
Study Arms (2)
Experimental group
EXPERIMENTAL6-week web-based nursing navigation programme
Control group
NO INTERVENTIONInterventions
health education guidance surveillance case management
Eligibility Criteria
You may qualify if:
- Being 30-70 years old,
- Not having been diagnosed with breast cancer,
- Not having been included in a breast health program before,
- Not having had a mammogram in the last year,
- Being at high risk of breast cancer according to the Tyrer-Cuzick Model,
- Having a phone, computer or laptop with internet access,
- Not having a health problem that prevents vision or hearing,
- Being willing to participate in the study.
You may not qualify if:
- Not being able to read or write,
- Having a history of breast cancer,
- Not being at high risk of breast cancer,
- Being pregnant or postpartum,
- Not agreeing to participate in the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Cancer early diagnosis screening and education center
Istanbul, Büyükçekmece, 34500, Turkey (Türkiye)
Family health center
Istanbul, Büyükçekmece, 34500, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Selda Seçginli, Prof. Dr.
Atlas University
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
- Lecturer
Study Record Dates
First Submitted
June 3, 2025
First Posted
June 11, 2025
Study Start
February 1, 2026
Primary Completion
May 1, 2026
Study Completion (Estimated)
September 30, 2026
Last Updated
May 1, 2026
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share