RecruitingNot ApplicableNCT06309290

Prehabilitation With Resistance-exercise Training for Breast Cancer Neoadjuvant Therapy

Prehabilitation Based on Resistance-exercise Training in Women With Breast Cancer Undergoing Neoadjuvant Therapy: From Molecular Mechanism to Clinical Benefits


Sponsor

Universidad de La Frontera

Enrollment

68 participants

Start Date

Jan 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Breast cancer stands as the foremost cause of cancer-related deaths among women worldwide, with the highest incidence of any cancer type. The choice of therapeutic interventions hinges upon factors like cancer stage, cell subtype, and tumor size. Consequently, individuals with more aggressive tumors, such as HER+2 and Triple Negative, or larger tumors often undergo neoadjuvant chemotherapy before breast surgery. However, these anticancer treatments come with side effects like cancer-related fatigue, reduced functional capacity, and changes in body composition, notably skeletal muscle atrophy. Skeletal muscle loss correlates with heightened mortality rates, cardiotoxicity, and diminished quality of life, underscoring the need for early therapeutic interventions. One such promising strategy is prehabilitation, which involves resistance-exercise training aimed at bolstering skeletal muscle mass from the outset of the disease, even preceding breast surgery. Resistance-exercise training has shown favorable effects on women undergoing adjuvant therapy or survivors of breast cancer, however, its molecular and clinical effects in women with breast cancer undergoing neoadjuvant therapy are unknown.


Eligibility

Sex: FEMALE

Plain Language Summary

Simplified for easier understanding

This study tests whether a structured exercise program — specifically resistance (strength) training — done before and during chemotherapy (neoadjuvant) can help breast cancer patients preserve muscle strength, reduce treatment side effects, and improve their readiness for surgery. This approach is called "prehabilitation." **You may be eligible if...** - You are a postmenopausal woman with stage I, II, or III breast cancer - Your doctor has recommended chemotherapy before surgery (neoadjuvant chemotherapy) - You are a candidate for curative breast surgery - Your BMI is between 18.5 and 30 - You are currently sedentary (not exercising regularly) **You may NOT be eligible if...** - You have conditions that make strength exercise unsafe (e.g., severe arthritis, neurological disorders, paralysis) - You have serious heart problems or poor heart pump function (ejection fraction below 50%) - You have received prior cancer treatment - You are taking nutritional supplements like protein powders, creatine, or omega-3 fatty acids Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERPrehabilitation with resistance-exercise training

The volunteers in the intervention group will be subjected to 16 - 20 weeks of whole-body resistance-type exercise training (2x/wk).

OTHERUsual care program

The volunteers in the intervention group will be subjected to usual care (diagnosis confirmation, chemotherapy treatment planning and an initial education session).


Locations(2)

Fundación Arturo López Pérez

Santiago, Chile

Department of Rehabilitation Sciences, Faculty of Medicine, Universidad de La Frontera. Temuco, Chile

Temuco, Chile

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NCT06309290


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