Clinical trial · Interventional
Risk Reduction Program for Women Having High Risk of Breast Cancer
The Effect of Risk Reduction Program Applied to Women With High Breast Cancer Risk on Participation in Screening, Health Beliefs and Behavior
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
An intervention program involving education, guidance, counseling, case management and surveillance based on the Health Belief Model will be implemented on women with high risk of breast cancer. The impact of the breast cancer risk reduction program on participation in breast cancer screenings, health beliefs (health motivation, sensitivity, fear of breast cancer) and behaviors (physical activity, nutrition, health responsibility, genetic counseling) will be evaluated in the study.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Cancer Screening | — | UNRESOLVED | — |
| Early Detection of Cancer | — | UNRESOLVED | — |
| Health Behavior | — | UNRESOLVED | — |
| Preventive Health Care | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Breast Cancer Risk Reduction Program (BrCaRRP) | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Intervention group (BrCaRRP)
- description
- Individual interventions based on the Health Belief Model and the The Health Promotion Model involving education, guidance, counseling, case management and surveillance for women with high breast cancer risk
- interventionNames
- Behavioral: Breast Cancer Risk Reduction Program (BrCaRRP)
- type
- NO_INTERVENTION
- label
- Control Group
- description
- An information note will be given to the control group. The post-tests will be collected at the end of 12 weeks
Primary outcomes (5)
- measure
- Breast Cancer Screening
- timeFrame
- 12 weeks
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 25 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * Volunteering to participate in the study * Being the first degree biological relative of a primary breast cancer patient diagnosed at or before the age of 50 * Aged 25 or older * No mammography and/or MRI in the last 18 months * Being literate Exclusion Criteria: * Having been diagnosed with breast cancer (first degree relative) * Being pregnant or breastfeeding
References
Publications (1)
- DERIVEDOzcelik H, Gozum S. The Effect of the Breast Cancer Risk Reduction Program on Women With High Breast Cancer Risk in Terms of Their Participation in Screening and Their Health Beliefs and Behavior: A Study Protocol for a Randomized Controlled Trial. Cancer Nurs. 2024 Nov-Dec 01;47(6):E376-E386. doi: 10.1097/NCC.0000000000001229. Epub 2023 Mar 13. PMID 36907899