Actively Recruiting
Influence of a Supervised Postpartum Exercise Program on Maternal Physical Activity Levels and Musculoskeletal Health
Led by Carroll University · Updated on 2026-05-29
50
Participants Needed
1
Research Sites
13 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying postpartum women to understand how a weekly exercise program affects physical activity, muscle strength, endurance, and pelvic floor function after childbirth. The study aims to improve physical activity habits, neuromuscular health, and overall wellbeing, including reducing fear of movement, improving sleep quality, and enhancing quality of life. This trial is important because many postpartum women face barriers to exercise, and the study allows incorporating children into exercise sessions to help overcome those challenges. Participants will be randomly assigned to either an exercise group or a control group. The exercise group will attend a 1-hour in-person group exercise session once a week for 8 weeks. The control group will not receive the exercise intervention but will complete weekly questionnaires about their physical activity. The program includes progressive exercise and assessments like strength testing, pelvic floor muscle function, and fatigue tasks. Childcare is offered, and participants may include their children in the exercise sessions. During the study, participants will undergo various assessments before and after the intervention, including measurements of physical activity levels using steps and activity counts, lower extremity strength, pelvic floor muscle strength and endurance, and sleep quality. Researchers will use clinical tests, questionnaires, and ultrasound imaging to evaluate muscle function and musculoskeletal health. The total involvement includes baseline and post-intervention assessments conducted around 7 to 14 days after the exercise program ends, helping to monitor changes in strength, endurance, and wellbeing.
CONDITIONS
Brief Title
Postpartum Exercise Intervention
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Gave birth in the 24 months prior to study enrollment
You will not qualify if you...
- Less than 6 weeks postpartum or not medically appropriate to engage in exercise regardless of time since childbirth
- Daily use of prescription anti-inflammatory or pain medications
- Significant orthopedic conditions contraindicating exercise or fatigue tasks
- Moderate to severe cardiovascular or pulmonary disease that prevents exercise participation
- Neuromuscular health conditions such as diabetes, neuropathy, multiple sclerosis, stroke, or seizures
- Smoking, vaping, or use of tobacco or nicotine products
- Use of any illegal drugs
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 - 8 weeks
Participants attend a supervised, progressive 8-week group exercise program to improve physical activity levels and musculoskeletal health.
1 weekly group exercise session (in-person)
Duration - 1 to 2 weeks
Participants complete follow-up assessments including physical activity questionnaires and neuromuscular function tests to evaluate outcomes after the exercise program.
1 to 2 visits (in-person)
Trial Site Locations
Total: 1 location
1
Carroll University Center for Graduate Studies
Waukesha, Wisconsin, United States, 53186
Actively Recruiting
Research Team
R
Rita Deering, DPT, PhD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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