Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
FEMALE
ID07284030

Effect of a 6-Week Web-Based Psychoeducation Program on Psychological Well-Being, Quality of Life, and Fear of Recurrence in Breast Cancer Survivors Who Completed Active Treatment

Led by Yasemin Nazli · Updated on 2025-12-16

72

Participants Needed

1

Research Sites

39 weeks

Total Duration

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AI-Summary

What this Trial Is About

Researchers are evaluating a web-based psychoeducation program designed to improve psychological well-being and quality of life in women who have survived breast cancer and completed active treatment at least one year prior. This randomized controlled trial aims to assess if the online program can reduce fear of cancer recurrence and hopelessness while enhancing coping skills and psychosocial adjustment during survivorship. Participants will be randomly assigned to one of two groups: one will receive a 6-week structured psychoeducation program delivered online through the website www.onkodestek.org combined with weekly live Zoom sessions lasting 30 to 45 minutes each, covering topics such as living with breast cancer, managing psychosocial challenges, improving quality of life, and fostering hope and meaning. The other group will receive standard care alone. After the study ends, those in the control group will have access to the psychoeducation platform. Throughout the study, participants will complete assessments at the start, immediately after the 6-week program, and again at a 2-month follow-up. These evaluations include measures of psychological well-being, fear of cancer recurrence, quality of life, and hopelessness using validated self-report tools. The study focuses on understanding the psychological benefits of web-based support during the post-treatment survivorship period for breast cancer survivors.

CONDITIONS

Official Title

Psychoeducation and Well-Being After Breast Cancer

Who Can Participate

Age: 18Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • 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

AI-Screening

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Trial Site Locations

Total: 1 location

1

Breast Cancer Outpatient Clinic

Istanbul, Turkey (Türkiye), 34740

Actively Recruiting

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Research Team

Y

Yasemin Nazlı, Clinical Nurse Specialist

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

Frequently Asked Questions

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Published Research Related To This Trial

A qualitative case study of body image in women with breast cancer participating in an exercise program.

Pau Mateu, Clara Teixidor-Batlle, María-Pilar Suárez-Alcázar...

https://pubmed.ncbi.nlm.nih.gov/41032141