Exercise Program on Pain, Physical Function, and Quality of Life in Breast Cancer Survivors (IO/2024)

Universidad de Burgos

Status: Active, not recruiting

Conditions: Female Breast Cancer

Treatments: Other: Exercise program

Study type: Interventional

Funder types: Other

Identifiers

NCT06618690

IO/2024 (Other Identifier)

Details and patient eligibility

About

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

Full 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.

Enrollment: 325 estimated patients

Sex: Female

Ages: 18 to 65 years old

Volunteers: No Healthy Volunteers

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.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

325 participants in 2 patient groups

Grupo experimental

Experimental group

Description:

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.

Treatment:

Other: Exercise program

group control

No Intervention group

Description:

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.