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/Actively Recruiting
Led by Yasemin Nazli · Updated on 2025-12-16
72
Participants Needed
1
Research Sites
6 weeks
Total Duration
This research aims to evaluate the effects of a web-based psychoeducation program on psychological well-being and quality of life in female breast cancer survivors who have completed active treatment at least one year ago and are currently in remission. It is a randomized controlled trial comparing the program plus standard care to standard care alone. The study focuses on important outcomes such as psychological well-being, fear of cancer recurrence, quality of life, and hopelessness. Participants will be randomly assigned to one of two groups one group will receive a 6-week online psychoeducation program alongside standard care, while the other group will receive only standard care. The program includes weekly live sessions lasting 30 to 45 minutes, delivered via Zoom through the www.onkodestek.org platform. These sessions cover coping strategies, psychosocial adjustment, quality of life improvements, psychological well-being, and fostering hope and meaning in life. During the study, participants will be assessed at baseline, immediately after the 6-week program, and again at a 2-month follow-up. Assessments include self-reported measures of psychological well-being, fear of cancer recurrence, quality of life, and hopelessness. Researchers will monitor these outcomes to understand the programs impact. After the study ends, those in the control group will be offered access to the psychoeducation platform. The total participation period includes the intervention and follow-up assessments.
CONDITIONS
Psychoeducation and Well-Being After Breast Cancer
Y
Yasemin Nazlı, Clinical Nurse Specialist
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Yasemin Nazli
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Duration - 6 weeks
Participants in the intervention group complete a 6-week web-based psychoeducation program with weekly live sessions via Zoom, addressing coping with breast cancer survivorship and psychological well-being. Control group participants continue standard care without the program during this period.
Weekly online sessions lasting 30-45 minutes
Duration - 2 months after treatment
Participants complete assessments on psychological well-being, fear of cancer recurrence, quality of life, and hopelessness at baseline, immediately post-intervention, and at 2-month follow-up to evaluate the effects of the psychoeducation program.
2 assessment visits (online or in-person)
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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Pau Mateu, Clara Teixidor-Batlle, María-Pilar Suárez-Alcázar...
https://pubmed.ncbi.nlm.nih.gov/41032141/Maria M Karsten, Robert Roehle, Sarah Albers...
https://pubmed.ncbi.nlm.nih.gov/35066338/Yasemin Nazli
Lead Sponsor