Ireland
--:--IST
Recruiting Not applicable

Physical Exercise During Preoperative Chemotherapy for Breast Cancer

NCT05184582 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2022-11-09
Last updated
2025-09-22

Condition(s) studied

Breast Cancer

Investigational drug(s) / intervention(s)

Physical training

Physical training: Participants randomized to the exercise group will complete two structured 60-min exercise sessions per week from initiation of NACT to surgery (approx. five months).

Study summary

Neoadjuvant chemotherapy (NACT) is increasingly used in breast cancer. The best proof of NACT efficacy is pathological complete response (pCR), i.e. the absence of invasive tumour on post-NACT surgical histopathology. While it is known that physical exercise can help patients to better tolerate and complete often harsh cancer treatments, it is an emerging area of research to understand if and how exercise exerts anti-tumour effects and improves oncological outcomes.

The main aim of the Neo-ACT trial is to examine if a physical exercise intervention during NACT can increase pCR rates in breast cancer. Secondary aims are residual cancer burden, radiological tumour response, patient-related outcomes (health-related quality of life, physical activity), physiological outcomes (muscle strength, cardiorespiratory fitness), cancer treatment-related toxicities (cognitive dysfunction, chemotherapy completion rates) and long-term sick leave. Furthermore, the trial will explore how physical exercise affects anti-tumoral mechanisms inherent to therapy or host by hypothesis-generating translational analyses.

712 patients with primary invasive breast cancer will be randomized to either a supervised intervention of high-intensity interval and resistance training during NACT, supported by an exercise app, or to usual care, and followed for two years. Physical activity is meticulously tracked. By offering patients active involvement, the trial contributes strongly to the concept of personalized medicine.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with primary invasive breast cancer cT1-T3 cN0-2 * Full tumour biology available before initiation of NACT * Oral and written consent * Age ≥ 18 years Exclusion Criteria: * Pregnancy or breast-feeding * Bilateral invasive breast cancer * The presence of musculoskeletal, neurological, respiratory, metabolic or cardiovascular conditions that may prevent safe completion of the exercise demands of the study * Currently performing equal to or more than 150 mins of moderate to high intensity aerobic exercise and 2 sessions per week of moderate intensity resistance exercise

Primary outcome measure(s)

  • Pathological complete response — 5-6 months
    Absence of residual invasive tumor in breast and axilla at surgery

Trial sites (13)

FacilityCityRegionStatus
Cabrini Health Melbourne Australia Not Yet Recruiting
Helsinki University Hospital Helsinki Finland Recruiting
Turku University Hospital Turku Finland Not Yet Recruiting
Karolinska University Hospital Stockholm Stockholm County Recruiting
Sahlgrenska University Hospital Gothenburg Sweden Recruiting
Skaraborgs sjukhus Lidköping Sweden Recruiting
Capio St Görans Hospital Stockholm Sweden Recruiting
Southern General Hospital Stockholm Sweden Recruiting
Sundsvall Hospital Sundsvall Sweden Recruiting
Umeå University Hospital Umeå Sweden Recruiting
Västmanlands Hospital Västerås Sweden Recruiting
Edinburgh Napier University Edinburgh Scotland Not Yet Recruiting
Royal Marsden London United Kingdom Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05184582 on ClinicalTrials.gov ↗ ← All trials in Sweden