Exercise Program on Pain, Physical Function, and Quality of Life in Breast Cancer Survivors

Efficacy of a Supervised Exercise Program on Pain, Physical Function, and Quality of Life in Breast Cancer Survivors: Protocol for a Randomized Clinical Trial

The purpose of this project is to develop a randomized clinical trial to determine the efficacy of a supervised exercise program on pain, physical function and quality of life in female breast cancer survivors

A randomized, double-blind, clinical trial will be conducted with 325 participants. The intervention group will receive a supervised exercise program for 12 weeks, while the control group will receive no intervention. Participants' pain, physical function and quality of life will be assessed at baseline, post-intervention and 12 weeks post-intervention.

Inclusion Criteria:

• women between 18 and 65 years of age,
• women with oncologic treatment completed less than 3 months ago,
• women without metastasis,
• women without pathologies that contraindicate exercise,
• women who have agreed to sign the informed consent form

Exclusion Criteria:

• not attending scheduled sessions to instruct on the exercises to be performed, - being part of other studies,
• undergoing another type of therapy
• pregnancy patients.