Breastmilk in Response to a Bout of Exercise

Overview

About this study

The purpose of this study is to unveil the mechanistic benefits of a bout of postpartum maternal exercise on infant health that are provided by breastmilk.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Female (≥ 18 years) that plan to breastfeed for >2 months
  • Able to comfortably perform moderate-intensity exercise

Exclusion Criteria:

  • Active coronary artery disease or heart failure. 
  • Participation in a structured exercise program ≥ 1 day/week in the “inactive” subcohort or < 3 days per week in the “active” subcohort.
  • A known medical condition that in the judgment of the investigator might interfere with the completion of the protocol such as the following examples:
    • Abnormal liver function test results (Transaminase >2 times the upper limit of normal
    • Abnormal renal function test results (calculated GFR <60 mL/min/1.73m2);
    • If on antihypertensive, thyroid, anti-depressant or lipid lowering medication, lack of stability on the medication for the past 2 months prior to enrollment in the study
    • Uncontrolled thyroid disease (TSH undetectable or >10 mlU/L); testing required within three months prior to admission for subjects with a goiter, positive antibodies, or who are on thyroid hormone replacement, and within one year otherwise
    • Abuse of alcohol or recreational drugs
    • Active tobacco smoking within the past 3 months
    • Infectious process not anticipated to resolve prior to study procedures (e.g. meningitis, pneumonia, osteomyelitis).
    • Uncontrolled arterial hypertension (Resting diastolic blood pressure >90 mmHg and/or systolic blood pressure >160 mmHg) at the time of screening.
    • A recent injury to body or limb, muscular disorder, use of any medication, any carcinogenic disease, or other significant medical disorder if that injury, medication or disease in the judgment of the investigator will affect the completion of the protocol
    • Active pregnancy
    • Restrictions on Use of Other Drugs or Treatments:
      • Any other medication believed to be a contraindication to the subject’s participation.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 06/06/2024. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Mark Pataky, Ph.D., M.S.

Open for enrollment

Contact information:

Devanshi Gupta

(507) 255-6752

Gupta.Devanshi@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20581312

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