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

Not Applicable

Active, not recruiting

• Conditions: Female Breast Cancer
• Interventions: Other: Exercise program

• Registration Number: NCT06618690
• Lead Sponsor: Universidad de Burgos

Brief Summary

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

Detailed Description

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.

Study Timeline

• Status Verified: 2024-09
• Study Start: 2024-09-10
• Study First Submitted: 2024-09-16
• Study First Submitted QC: 2024-09-27
• Last Update Submitted: 2024-09-27
• Study First Posted: 2024-09-30
• Last Update Posted: 2024-09-30
• Primary Completion: 2025-02-01
• Study Completion: 2025-04-02

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: Female
• Target Recruitment: 325

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.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Grupo experimental	Exercise program	The participants will be recruited through the oncologists of the Hospital Universitario Torrecárdenas (Almería). The proposal will be carried out in the intervention group (group 1), while the control group (group 2) will undergo the conventional recommendations indicated for this type of patients.

Primary Outcome Measures

Name	Time	Method
repeated measures ANOVA	12 weeks	the range of motion, tone and muscle strength of the group will be measured in 3 measures over the 12 weeks

Trial Locations

Locations (1)

Hospital Universitario Torrecárdenas; 🇪🇸 Àlmeria, Alemeria, Spain