A Study to Evaluate the Impact of Menopause on Blood Pressure Regulation During Exercise

Overview

About this study

The purpose of this study is to determine how menopause influences blood pressure responses during exercise in women.

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:

Healthy Adults

  • Healthy women (≥ 18 years of age).
  • Participants will be categorized by menopausal status using the STRAW+10 guidelines36:
    • Premenopausal women will be experiencing regular menstrual cycles; 
    • Perimenopausal women will be experiencing irregular cycles (i.e., early perimenopause) or 2-11 mo of amenorrhea (i.e., late perimenopause). Postmenopausal women will have been > 5 years without menstruation and have undergone natural menopause.
  • No history of cardiovascular, pulmonary, neurologic, orthopedic, or other diseases affecting the neuromuscular system.
  • Undergoing treatment for menopausal symptoms (e.g., hormone replacement therapy).
  • Having taken oral contraceptives in the past > 6 months.
  • BMI ≤ 35kg/m^2.
  • Current non-smokers with smoking history < 15 pack years.
  • Able to engage in exercise (i.e., without significant orthopedic limitations or musculoskeletal disorders limiting their ability to exercise).

Patients with Hypertension

  • (≥ 18 years).
  • No history of dangerous arrhythmias.
  • Not pacemaker dependent.
  • Undergoing treatment for menopausal symptoms (e.g., hormone replacement therapy).
  • Having taken oral contraceptives in the past > 6 months.
  • Body mass index ≤ 35 kg/m^2.
  • Currently non-smokers with < 15 pack year history.
  • Able to exercise (i.e., without significant orthopedic limitations or musculoskeletal disorders limiting their ability to exercise).
  • Patients will be tested while receiving optimized standard pharmacologic optimized therapy.
  • All patients will be managed by their primary care physician or cardiologist with additional review by Dr. Borlaug (Co-Investigator) prior to enrollment to ensure inclusion and exclusion criteria have been satisfied and participation in exercise testing is safe.

Exclusion Criteria:

  • History of dangerous arrhythmias.
  • Undergoing treatment for menopausal symptoms (e.g., hormone replacement therapy.
  • Having taken oral contraceptives in the past > 6 months.
  • Body mass index > 35 kg/m^2.
  • Current smokers and/or smoking history > 15 pack years.
  • Pregnant women.
  • Uremia, history of allergy to iodides.
  • Impaired renal function.
  • Creatinine value than or equal to 1.3 mg/dL (via clinical record within the past 6 months).
  • Diagnosis of liver disease.
  • Individuals who are not able to engage in exercise.
  • For individuals agreeing to undergo dual energy x-ray absorptiometry (DEXA) scanning for measurement of body composition as part of their study visit, additional exclusion criteria apply:
  • Recently administered gastrointestinal contrast or radionuclides;
  • Severe degenerative changes or fracture deformity in measurement areas; or
  • Inability to attain correct position and/or remain motionless for the measurement period.

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

Thomas Olson, Ph.D., M.S.

Open for enrollment

Contact information:

Eric Bruhn M.A.

(507) 266-2690

Bruhn.Eric@mayo.edu

More information

Publications

Publications are currently not available