Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05297773

Resistance vs. Aerobic Training on Breast Cancer Patients Undergoing Neoadjuvant Treatment

Led by Fundacao Champalimaud · Updated on 2025-02-26

132

Participants Needed

2

Research Sites

158 weeks

Total Duration

On this page

Sponsors

F

Fundacao Champalimaud

Lead Sponsor

F

Faculdade de Motricidade Humana - Universidade de Lisboa

Collaborating Sponsor

AI-Summary

What this Trial Is About

A recent consensus study suggested that understanding the impact of exercise on the tumor microenvironment and therapy effectiveness is paramount and should be considered as a research priority. Therefore, the research team intends to address some of the scientific challenges proposed, which represent clear gaps in the current knowledge. The investigators propose a randomized controlled trial conducted during all neoadjuvant treatment duration that aims to evaluate and compare the effects of two different exercise protocols (aerobic and resistance training) against a relaxation control group on Ki-67% changes as the main outcome in breast cancer patients. Secondary outcomes will be body composition; resting metabolic rate; physical fitness; quality of life, fatigue, depression/anxiety; accelerometry data (physical activity levels, sedentary time); sleep quality; tumor biology (size, hypoxia, and immune profile); glycemic, lipid, and inflammatory profile. This project will help not only researchers with the design of future exercise intervention protocols but will also help exercise physiologists in the decision-making process when defining training programs. Moreover, the investigators expect that this research program will encourage more cancer patients to exercise. The team expects that patients with breast cancer engaging in structured exercise will show a more marked decrease in Ki-67, tumor size, and hypoxia and increase the tumor-infiltrating lymphocytes (TILs) compared to controls. The investigators anticipate a more noticeable decrease in the preoperative endocrine prognostic index (PEPI) score and in the Residual Breast Cancer (RCB) in both training groups (respectively with hormonal and chemotherapy). Also, frequent declines in physical fitness are expected to be mitigated in exercisers. It is hypothesize that aerobic training will ameliorate cardiorespiratory fitness and fat mass, while the effects of resistance training will be more relevant for muscle strength, muscle mass, and bone health. Both exercise groups will show greater improvements in quality of life, fatigue, depression, anxiety, and sleep quality. Regarding glycemic, lipid, and inflammatory profiles, the investigators expect to see more favorable changes in both training groups, with a more evident decrease in fasting glucose and insulin, HbA1c%, total and LDL-cholesterol, and triglycerides, and the increase in HDL-cholesterol. The increase in C-reactive protein (CRP), tumor necrosis factor -α (TNF-α), interleukin-6 (IL-6), IL-8, IL-1β, IL-1ra, and insulin-like growth factor-1 (IGF-1) and the decrease in brain-derived neutrotophic factor (BDNF), IL-12p70, IL-10, oncostatin M will be smaller in exercise groups.

CONDITIONS

Official Title

Resistance vs. Aerobic Training on Breast Cancer Patients Undergoing Neoadjuvant Treatment

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Histologically confirmed breast cancer (stage 0-III) scheduled for neoadjuvant chemotherapy or endocrine therapy
  • Women aged 18 years or older and not pregnant
  • Not involved in any structured exercise program in the past 6 months
  • Medical approval to participate in exercise
  • Willingness to attend exercise sessions
Not Eligible

You will not qualify if you...

  • Treated for any cancer in the past 5 years except basal cancer
  • Uncontrolled heart disease, including heart failure, coronary heart disease, or hypertension
  • Diabetes mellitus
  • Lung conditions such as chronic obstructive or restrictive pulmonary disease
  • Psychological disorders including dementia, Alzheimer's, or Parkinson's disease
  • Severe disability or any medical condition preventing exercise training
  • Alcohol or drug abuse

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Faculdade de Motricidade Humana - Universidade de Lisboa

Lisbon, Cruz-Quebrada, Portugal, 1495-751

Active, Not Recruiting

2

Fundação Champalimaud

Lisbon, Lisbon District, Portugal, 1400-038

Actively Recruiting

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Research Team

M

Maria-João Cardoso, MD

CONTACT

L

Luís B Sardinha, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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