Breast Cancer Exercise Intervention Study

NCT05957068 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2156

Last updated 2025-09-05

No results posted yet for this study

Summary

This is a 24-week exercise programme consisting of aerobic exercise and muscle strength training, 3 sessions per week. The first 9 sessions are supervised by physiotherapists in person, followed by 63 sessions monitored remotely (video) or supervised by trainers at ActiveSG (Sport Singapore) gyms.

Conditions

Interventions

BEHAVIORAL

Exercise Programme

Aerobic exercise consists of 20-minute brisk walks or jogs (5-6 km/h) on the treadmill each session, reaching a heart rate corresponding to 50%-70% of the patient's VO2max (VO2max is determined before embarking on the exercise programme). Study participants are expected to aim for 50% VO2max at the start of the exercise programme, and gradually increasing to 70% VO2max in subsequent exercise sessions. Strength training comprises a series of circuit resistance exercises targeting the major muscle groups. Patients will perform 2-4 sets of these exercises each session, 8-10 repetitions per set. Both aerobic exercise and strength training are done in the same session. With warm-up and cool-down, each session is estimated to take up 1 hour.

BEHAVIORAL

Control

Usual care group.

Sponsors & Collaborators

  • Singapore Cancer Society

    collaborator OTHER
  • Genome Institute of Singapore

    collaborator OTHER
  • National University of Singapore

    collaborator OTHER
  • Singapore General Hospital

    collaborator OTHER
  • National Cancer Centre, Singapore

    lead OTHER

Principal Investigators

  • Dr Elaine LIM, MD, PhD · National Cancer Centre, Singapore

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
99 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-01
Primary Completion
2028-05-31
Completion
2033-05-31

Countries

  • Singapore

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05957068 on ClinicalTrials.gov