Actively Recruiting
Investigating Resistance Training for Vascular Function and Quality of Life in Perimenopausal Women
Led by University of Michigan · Updated on 2025-07-11
50
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Women going through perimenopause, the transition period before menopause, often experience worsening blood vessel health, mood changes, sleep problems, and reduced quality of life. This trial investigates whether resistance exercise, such as lifting weights, can improve blood vessel function and these other health aspects in women aged 40 to 60 who are starting menopause. Researchers aim to understand how resistance training affects cardiovascular risk factors during this important life stage. Participants will be randomly assigned to one of two groups. One group will perform resistance training twice a week for 16 weeks, starting with lighter weights and gradually increasing intensity. Each session includes warm-up, stretching, and exercises targeting major muscle groups. The other group will receive weekly emails with general menopause information and maintain their usual lifestyle. After 16 weeks, both groups will have assessments repeated to compare effects. Throughout the study, participants will undergo tests of vascular function and endothelial function at the start and end. They will provide blood and urine samples and complete surveys about their mood, sleep quality, and menopause-specific quality of life. The study monitors adherence to exercise and evaluates changes in these measures to assess impacts of the training program. Participation lasts for 16 weeks with follow-up assessments at the University of Michigan.
CONDITIONS
Brief Title
Hemodynamics After Resistance Training
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Are between 40-60 years old
- Have had menstrual irregularities in the last 12 months
- Do not currently complete more than two 30-min sessions of structured exercise per week and do not do any resistance training exercise
- Are not currently pregnant
- Are able to exercise and your doctor has not told you that you cannot
- Can attend a morning study visit at the University of Michigan's School of Kinesiology Building
- Are willing to avoid food 2 hours prior to the morning study visit
- Are willing to avoid strenuous exercise, caffeine, and alcohol 8 hours prior to the morning study visit
- Are willing to participate in an exercise training program or health education program for 16 weeks
You will not qualify if you...
- Smoke or vape nicotine or marijuana
- Have had an oophorectomy, hysterectomy, or surgical menopause
- Are currently taking hormone replacement therapy
- Have taken hormone replacement therapy in the last 6 months
- Are taking steroidal medication or medication to treat diabetes, cholesterol, or high blood pressure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants complete baseline vascular function and exercise testing, provide blood and urine samples, and complete surveys about sleep, mood, and menopause-specific quality of life.
1 visit (in-person)
Duration - 16 weeks
Participants randomized to resistance training complete two strength training sessions per week for 16 weeks. Control group participants receive weekly health education emails and maintain current lifestyle habits.
Twice weekly sessions for resistance training group; weekly emails for control group
Duration - 1 day
Participants complete post-intervention vascular function and exercise testing, and the same surveys on sleep, mood, and menopause-specific quality of life as at baseline.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
University of Michigan School of Kinesiology
Ann Arbor, Michigan, United States, 48109
Actively Recruiting
Research Team
M
Marnie K. McLean, M.S.
A
Abbi D. Lane, Ph.D.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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