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Prospective Study of EXErcise Regimens After Treatment for Breast Cancer for Hypertrophy and Conditioning (EXERT-BCHC)

A

Allegheny Health Network (AHN)

Status

Enrolling

Conditions

Breast Cancer
Cancer

Treatments

Other: 6-12-25 Training Regimen
Other: 5/5/5 Cluster Set Training Regimen
Other: 8x8 Training Regimen
Other: Double Training Regimen

Study type

Observational

Funder types

Other

Identifiers

NCT07023887
2025-076-SG

Details and patient eligibility

About

This study investigates the impact of four standard of care, monitored group exercise regimens (resistance training) on conditioning and hypertrophy in women previously treated for breast cancer. The study will compare two conditioning regimens (6-12-25 and 8x8) and two hypertrophy regimens (5/5/5 cluster sets and double training) to assess changes in VO2 max, muscle mass, and fat mass.

Enrollment

15 estimated patients

Sex

Female

Ages

20 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 20-89 years
  2. Women prescribed exercise as a Standard of Care
  3. Women with a biopsy proven diagnosis of ductal carcinoma in situ (DCIS) or invasive carcinoma of the breast
  4. Women must have undergone treatment for breast cancer, including one or more of the following: surgery, radiation therapy, chemotherapy, immunotherapy, or hormonal therapy.
  5. Women undergoing active chemotherapy are not allowed on study. Immunotherapy or targeted agent usage is allowed.
  6. Women with > 6 months of resistance training experience under expert guidance by a CSCS

Exclusion criteria

  1. Any current treatment with cytotoxic chemotherapy for breast cancer
  2. Inability to safely engage in group sessions of resistance training as deemed by study Pl
  3. Severe arthritic, joint, cardiovascular, or musculoskeletal condition deemed by Pl to be unsafe to engage in resistance training
  4. Beta blocker or GLP-1 inhibitor medications
  5. Pregnant women
  6. Males

Trial contacts and locations

1

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Central trial contact

Clinical Trials Contact

Data sourced from clinicaltrials.gov

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