Exercise Program for Breast Cancer Survivors
(B-REP Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to explore the benefits of a tailored exercise program for Black breast cancer survivors. Participants will either join a 12-week supervised exercise program focused on resistance training or receive health education materials. The goal is to determine how exercise can improve health outcomes after cancer treatment. This trial suits Black or African American women who have completed breast cancer treatment in the last five years and are not currently following a regular resistance exercise routine. As an unphased trial, it offers a unique opportunity to contribute to research that could enhance recovery and quality of life for future survivors.
Will I have to stop taking my current medications?
The trial does not specify whether you need to stop taking your current medications. However, it mentions that ongoing hormonal therapy is acceptable, so you may be able to continue some treatments.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research has shown that exercise programs for breast cancer survivors are generally safe and manageable. These programs can enhance physical health and quality of life by reducing fatigue and pain while boosting overall well-being. Participants often find these programs helpful, as they are typically tailored to individual strength levels.
For instance, one study found that a personalized exercise plan reduced fatigue and pain while improving health-related quality of life. Another study demonstrated that clear communication about exercise increased participation and enhanced quality of life for breast cancer survivors.
Overall, these exercise programs are designed to be safe, and many participants find them beneficial. While experiences can vary, most people manage these exercise activities well.12345Why are researchers excited about this trial?
Researchers are excited about the individualized exercise program for breast cancer survivors because it tailors resistance exercises specifically to each participant's strength levels, which is a unique approach compared to standard physical activity guidelines. While most exercise recommendations for cancer survivors are generalized, this program customizes the intensity and type of exercises using the FITT principle (frequency, intensity, time, and type), potentially leading to better outcomes in muscle strength and overall health. By aligning with cancer-specific exercise recommendations, this program may offer a more effective way to enhance recovery and improve quality of life for breast cancer survivors.
What evidence suggests that this exercise program is effective for breast cancer survivors?
Research has shown that personalized exercise programs, like the one tested in this trial, can greatly benefit breast cancer survivors. One study found that a 12-week exercise program improved body shape and reduced tiredness, pain, and breathing problems. In this trial, participants in the intervention arm will receive a supervised exercise program, supporting findings that supervised exercise aids recovery for breast cancer patients. Additionally, personalized exercise routines during cancer treatment have been shown to lower the chances of emergency room visits and hospital stays. Overall, these findings suggest that tailored exercise programs can significantly enhance the physical health and quality of life for breast cancer survivors.12567
Who Is on the Research Team?
Angela Fong, PhD
Principal Investigator
University of Michigan Rogel Cancer Center
Are You a Good Fit for This Trial?
This trial is for Black or African American women over 18 who've had breast cancer stages 0I to IIIA and finished primary treatment within the last 5 years. They should not be currently meeting exercise guidelines, but can't join if they have metastatic disease, are pregnant, planning surgery, moving out of the US during the study period, or unable to increase exercise safely.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Baseline Assessment
Baseline assessments conducted before intervention
Treatment
Participants undergo a 12-week exercise intervention or health education control
Post-intervention Assessment
Assessments conducted immediately after the 12-week intervention
Follow-up
Participants are monitored for outcomes 3 months post-intervention
What Are the Treatments Tested in This Trial?
Interventions
- Control Arm
- Individualized exercise program
Individualized exercise program is already approved in United States, Canada, European Union for the following indications:
- Breast cancer rehabilitation
- Improvement of quality of life in cancer survivors
- Breast cancer rehabilitation
- Improvement of quality of life in cancer survivors
- Breast cancer rehabilitation
- Improvement of quality of life in cancer survivors
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Michigan Rogel Cancer Center
Lead Sponsor