Health Trials

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

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)

Trial design

Treatments tested in this trial

  • Web-Based Psychoeducation Program

Treatment groups

72 Participants
are divided into 2 treatment groups

Locations

1
Breast Cancer Outpatient Clinic34740, Istanbul Turkey (Türkiye)

Sponsors and collaborators

Yasemin Nazli

Lead sponsor

Uskudar University

Sponsor institution

Source ClinicalTrials.gov