The Effect of a Web-Based Supportive Psychoeducation Program on Psychological Well-Being, Quality of Life and Fear of Recurrence Applied to Patients Who Completed Active Breast Cancer Treatment

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Turkey
Breast Cancer Outpatient Clinic
RECRUITING
Istanbul
Contact Information
Primary
Yasemin Nazlı, Clinical Nurse Specialist
yasemin.nazli@st.uskudar.edu.tr
+905325025158
Time Frame
Start Date: 2025-05-01
Estimated Completion Date: 2026-02-01
Participants
Target number of participants: 72
Treatments
Experimental: Intervention Group
Participants receive a 6-week web-based psychoeducation program plus standard care
No_intervention: Control Group
Participants receive standard care only
Related Therapeutic Areas
Sponsors
Leads: Yasemin Nazli

This content was sourced from clinicaltrials.gov

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