Clinical trial Recruiting at 1 site Interventional Ages 20 to 89 Women only

Myokines and exercise after breast cancer treatment

Official title: Myo-EXERTBC: A Pilot Study Assessing Myokines During an EXErcise Regimen After Treatment for Breast Cancer

Run by Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute) · NCT07698314 · Data updated 2026-11-12

This pilot study tests how different resistance exercise programs affect myokine production in women who have completed breast cancer treatment.

More Breast Cancer trials

Quick facts

Study typeInterventional
Ages20 Years to 89 Years
SexWomen only
Enrollment21 (estimated)
SponsorAllegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)
Academic / other
Drugs / interventionschemotherapy, immunotherapy, radiation
Locations2 sites (Pittsburgh, Pennsylvania and 1 other locations)
StatusRecruiting
StartedJuly 6, 2026
Main results expectedJuly 2027
Study endsJuly 2028
Registry record updatedSeptember 30, 2026
Trial IDNCT07698314 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Women aged 20–89 who have completed breast cancer treatment and have prior supervised resistance training experience and are prescribed exercise as standard of care.

Probably not a fit

Women currently undergoing cytotoxic chemotherapy or unable to safely participate in group resistance training may be less likely to benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional pilot study will compare several resistance training regimens to see how they influence myokine production in women with a history of breast cancer. Participants are women aged 20 to 89 who have completed treatment and have at least three months of guided resistance training experience. The exercise programs include conditioning, strength, and hypertrophy resistance training, delivered in group sessions at the Allegheny Health Network Exercise Oncology Center. Immunotherapy or targeted agents are allowed, but active cytotoxic chemotherapy is not permitted during participation.

Why it matters

Potential benefit: If successful, the study could clarify how different resistance exercise prescriptions influence myokine responses, potentially informing personalized exercise plans for breast cancer survivors.

How similar studies have gone: Prior studies in exercise oncology have shown that exercise can modulate myokines, but this specific comparison of regimens in breast cancer survivors is exploratory and relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Age 20-89 years
2. Women prescribed exercise as a SOC
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. Women undergoing active chemotherapy are not allowed on study. Immunotherapy or targeted agent usage is allowed.
5. Women with \> 3 months of resistance training experience under expert guidance at the Allegheny Health Network Exercise Oncology Center

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 PI
3. Severe arthritic, joint, cardiovascular, or musculoskeletal condition deemed by PI to be unsafe to engage in resistance training
4. Pregnant women
5. Males

Where it's running

  • Allegheny General Hospital
    Pittsburgh, Pennsylvania, United States
    Recruiting
  • AHN Allegheny General Hospital
    Pittsburgh, Pennsylvania, United States
    Not yet recruiting

Study contacts

  • Principal investigator: Colin Champ, MD — AHN Radiation Oncology
  • Study coordinator: Clinical Trials Contact
  • Email: ctgov@ahn.org
  • Phone: 412-330-6151

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.