Clinical trial Recruiting at 2 sites Interventional Women only

Prehabilitation with resistance training for women with breast cancer before surgery

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

Run by Universidad de La Frontera · NCT06309290 · Data updated 2026-11-12

This study tests if a structured resistance training program can help postmenopausal women with breast cancer improve their muscle strength and quality of life before surgery compared to those who only receive standard care.

More Breast Cancer trials

Quick facts

Study typeInterventional
SexWomen only
Enrollment68 (estimated)
SponsorUniversidad de La Frontera
Academic / other
Drugs / interventionschemotherapy
Locations2 sites (Santiago and 1 other locations)
StatusRecruiting
StartedJanuary 1, 2025
Main results expectedAugust 2026
Study endsDecember 2026
Registry record updatedJune 12, 2026
Trial IDNCT06309290 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are postmenopausal women with stage I, II, or III breast cancer who are sedentary and eligible for neoadjuvant chemotherapy.

Probably not a fit

Patients with severe comorbidities affecting muscle metabolism or mobility, or those with previous antineoplastic treatment, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effects of prehabilitation through resistance-exercise training in postmenopausal women with breast cancer undergoing neoadjuvant therapy. The study aims to compare the outcomes of participants receiving usual care versus those engaging in a structured resistance training program over 16-20 weeks prior to surgery. The primary focus is on increasing skeletal muscle mass and improving overall physical performance and quality of life. Participants will be randomly assigned to either the prehabilitation group or the control group, with assessments conducted before and after the intervention.

Why it matters

Potential benefit: If successful, this approach could enhance muscle mass and improve recovery outcomes for women undergoing treatment for breast cancer.

How similar studies have gone: Other studies have shown promising results with prehabilitation and resistance training in cancer patients, suggesting potential for success in this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Postmenopausal women with breast cancer in stages I, II and III with luminal breast tumor, HER2+ or TNBC
* Indication for neoadjuvant chemotherapy
* Candidates for curative breast surgery
* Body mass index: 18.5 \<BMI \<30 kg/m2
* Sedentary (does not perform scheduled or planned physical activity ≥ 2 times a week)
* Willingness to participate in the study and follow the proposed prehabilitation scheme.

Exclusion Criteria:

* Present comorbidities that interact with the metabolism and mobility of the muscles of the body and that do not allow the (safe) performance of strength exercises (e.g., debilitating arthritis, all neurological disorders, paralysis, among others).
* Severe or uncontrolled cardiovascular disease, cardiac ejection fraction less than 50%
* Previous antineoplastic treatment
* Use of nutritional supplements (leucine, glutamine, casein, whey protein, fatty acids and creatine).

Where it's running

  • Fundación Arturo López Pérez
    Santiago, Chile
    Recruiting
  • Department of Rehabilitation Sciences, Faculty of Medicine, Universidad de La Frontera. Temuco, Chile
    Temuco, Chile
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.