Psychoeducation and Well-Being After Breast Cancer
Recruiting · NCT07284030 · Interventional (participants receive a specific treatment) · Lead sponsor: Yasemin Nazli
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
This randomized controlled trial evaluates the effectiveness of a web-based psychoeducation program on psychological well-being and quality of life in breast cancer survivors who completed active treatment at least one year earlier. Seventy-two women will be randomly assigned to either a 6-week online psychoeducation program plus standard care or standard care alone. The intervention consists of weekly 30-45 minute online sessions focusing on coping strategies, psychosocial adjustment, quality of life, and psychological well-being. Primary outcomes include psychological well-being, fear of cancer recurrence, quality of life, and hopelessness, assessed at baseline, post-intervention, and 2-month follow-up.
Who can take part
Inclusion criteria
- Female breast cancer survivors
- Completed active breast cancer treatment (surgery, chemotherapy, radiotherapy) at least 12 months ago
- Currently in remission (no evidence of active disease)
- Age between 18-65 years
- Able to read and write Turkish
- Access to computer or smartphone with internet connection
- Able to participate in online video sessions via Zoom
- Willing to provide informed consent
Exclusion criteria
- Current cancer recurrence or metastatic disease
- Active psychiatric disorder requiring treatment
- Cognitive impairment that prevents participation in online sessions
- Currently receiving active cancer treatment (excluding hormonal therapy)
- Participation in another psychosocial intervention study
- No internet access or inability to use web-based platforms
- Male breast cancer patients
- Unable to commit to 6-week program schedule
Where it is running
1 location listed.
- Breast Cancer Outpatient Clinic - Istanbul, Turkey (Türkiye)