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Search / Trial NCT05073224

Muscle Function After Childbirth

Launched by CARROLL UNIVERSITY · Sep 28, 2021

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial, titled "Muscle Function After Childbirth," is studying how childbirth affects muscle control and strength in women. The researchers want to understand the differences in muscle function between women who have given birth for the first time (postpartum) and women who have never been pregnant (nulligravid). In total, 78 women will participate, attending two sessions about a week apart to undergo tests that measure their muscle strength and control in the legs and trunk, as well as their levels of physical activity.

To be eligible for this study, women must be postpartum after their first child and generally healthy. However, those with certain health conditions, like significant orthopedic issues or chronic diseases, won’t be able to participate. Women who have never been pregnant can also join as control participants, provided they meet similar health criteria. If you decide to take part in this study, you can expect to complete some assessments related to your muscle function, helping researchers learn more about postpartum recovery and muscle health.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Post-partum
  • Primiparous (this is their first child)
  • Exclusion Criteria:
  • multiple gestation
  • prescription anti-inflammatory/pain medications that are taken daily
  • significant orthopedic conditions that would contraindicate performance of the fatigue task (such as fractures, severe scoliosis, etc)
  • cardiovascular \& pulmonary disease
  • neuromuscular health conditions (such as diabetes, neuropathy, multiple sclerosis, stroke, seizures, etc)
  • history of previous abdominal surgery (with the exception of Cesarean delivery)
  • Nulligravid Women (Controls)
  • Women from the surrounding community will also be recruited to serve as controls
  • Nulligravid women will meet the same inclusion/exclusion criteria as the postpartum women, with the exception of never having been pregnant

About Carroll University

Carroll University, a distinguished institution dedicated to advancing health sciences education and research, serves as a clinical trial sponsor committed to fostering innovative medical research and improving patient outcomes. With a strong emphasis on collaboration and ethical standards, Carroll University leverages its academic expertise and state-of-the-art facilities to conduct rigorous clinical trials that address critical health challenges. The university's multidisciplinary approach ensures comprehensive oversight and a commitment to translating research findings into practical applications, ultimately enhancing the quality of care in the communities it serves.

Locations

Madison, Wisconsin, United States

Waukesha, Wisconsin, United States

Patients applied

0 patients applied

Trial Officials

Rita Deering, PT, DPT, PhD

Principal Investigator

Carroll University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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