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NCT Number: NCT06309290

Prehabilitation With Resistance-exercise Training for Breast Cancer Neoadjuvant Therapy

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.

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Key information

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Fundación Arturo López Pérez, Santiago, Chile

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About this study

Hypothesis: Prehabilitation based on resistance-exercise training before surgery in women with breast cancer undergoing neoadjuvant therapy increases skeletal muscle mass compared with usual care.

Secondary, prehabilitation based on resistance-exercise training before surgery in women with breast cancer undergoing neoadjuvant therapy generates better results in body composition, physical performance, clinical parameters (serious adverse events, hospital readmission, infection, complications), physiological parameters and quality of life at one-month hospital discharge compared to usual care.

Objective: To determine the effects of prehabilitation based on resistance-exercise training versus usual care, before and after breast surgery, on skeletal muscle mass in women with breast cancer undergoing neoadjuvant chemotherapy.

Methodology: A single-blind, randomized controlled clinical trial will be developed. Sixty-eight postmenopausal women with stage I, II and III breast cancer with HER2+ type breast tumor and Triple negative breast cancer undergoing neoadjuvant therapy and with an indication for breast surgery will be divided into two groups: usual care (CONTROL, n=34) versus Prehabilitation (P-REHAB, n=34). All participants will receive an education session 20 weeks before surgery + neoadjuvant chemotherapy for 16-20 weeks as is normally done for this type of patien. Only participants in the P-REHAB group will undergo 16-20 weeks of whole-body resistance-exercise training (twice a week). At baseline, after prehabilitation program and 4 weeks after surgery, the cross-sectional area of the quadriceps muscle and of the muscle region at lumbar level 3 will be determined by CT-Scan. Also, fasting blood samples will be obtained to measure biochemical and molecular markers (e.g. miRNAs). Maximal strength will be determined by 1 repetition maximum (1RM) leg press, leg extension, lat pull down, chest press, horizontal row, and handgrip. In addition, physical performance will be assessed with the short physical performance battery (SPPB), functional capacity with the 6-minute walk test, quality of life with the BR23 questionnaire, and cancer-related fatigue with the Brief Fatigue Inventory scale at the same time points. Finally, samples from tumor breast cancer and pectoralis muscle will be obtained on the day of breast surgery.

Expected results: It is expected that prehabilitation based on resistance-exercise training results in increased muscle mass in women with breast cancer undergoing neoadjuvant chemotherapy compared to participants receiving usual care. Also, it is expected that this intervention before surgery in women with breast cancer undergoing neoadjuvant therapy will generate better results in clinical parameters (serious adverse events, hospital readmission, infection, complications) and quality of life one month after hospital discharge compared to usual care . These results will allow the creation of local, regional, national and international strategies to combat the adverse effects of breast cancer and its antineoplastic treatment, especially in women with more aggressive breast cancer.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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).

Treatment and study plan

Prehabilitation with resistance-exercise training

Other

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

Other names: Prolonged resistance-type exercise training, Prehabilitation

Usual Care Program

Other

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

Other names: Standard therapy

Primary outcomes

  1. Change in skeletal muscle mass (measured via Computed tomography (CT) scan)

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    Cross-sectional area of the quadriceps via single-slice CT scan

Secondary outcomes

  1. Change in arms and legs strength (measured via 1-Repetition Maximum (1RM) testing)

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    Maximal strength assessment via 1RM testing of horizontal row, lat pull down, chest press, leg press, and leg extension)

  2. Change in hand grip strength (measured via JAMAR handheld dynamometer)

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    Maximal strength assessment via 1RM testing of JAMAR handheld dynamometer.

  3. Change in physical performance measured via Short physical performance battery

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    Measurement of physical performance via SPPB Short physical performance battery (0 to 12 points, whether higher scores mean a better outcome).

  4. Change in points quality of life measured via questionnaire European Organisation for Research and Treatment of Cancer (EORTC QLQ-C30)

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    Measurement of quality of life via EORTC QLQ-30, this questionnaire has 30 question covering functional state and cancer related symptoms. Besides, there are two specific question covering the "overall health" and "overall quality of life". The scores obtained are standardized and a score between 0 and 100 is obtained. High values on the global health and functional status scales indicate a better quality of life. However, high values on the symptom scale indicate a lower quality of life

  5. Change in points Brief fatigue inventory (BFI)

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    The instrument consists of nine items, each rated on a scale from 0 to 10, aimed at assessing fatigue. By averaging the scores of all items, a fatigue score is derived, wherein higher values signify more severe fatigue.

  6. Change in microgram per milliliter (µg/ml) of Human Insulin via ELISA

    Time frame: Before training (week 0), and after training (up to 20 weeks) and 4 weeks post surgery

    Measurement in blood samples, the insulin will evaluate by ELISA using the Human Insulin ELISA Kit, following the manufacturer's recommendations

  7. Change in pathological complete response rate

    Time frame: Before training (week 0), and after training (up to 20 weeks)

    Measured according to Sataloff criteria.

  8. Change quantification proteins

    Time frame: Before training (week 0), and after training (up to 20 weeks)

    It will be measured from a muscle sample obtained at the time of surgery using the western blot technique.

Study contacts

Contact information is provided by the study sponsor or research team.

Gabriel N Marzuca-Nassr, PT, MSc, PhD

CONTACT

[email protected]

+56 45 2596713

Macarena Artigas, PT, MSc

CONTACT

[email protected]

990420698

Sponsors and collaborators

Lead sponsor

Universidad de La Frontera

Other

Registry information

Official study title

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

Acronym: NEO STRONG

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 13, 2024
Registry last updated
Jun 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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