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New study probes postpartum muscle fatigue and pelvic pain

NCT ID NCT05073224

Knowledge-focused Sponsor: Carroll University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused This study
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study compares muscle control and pelvic stability in women who have given birth to their first child and women who have never been pregnant. Researchers will measure how long women can hold a leg raise, how steady their leg is, and any pain or difficulty they feel. The goal is to better understand muscle fatigue and weakness after childbirth.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 78 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2022

Expected to finish

Jul 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

20 to 35 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Muscle Weakness puerperal disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Force steadiness Muscle fatigue Muscle weakness Nulligravid Postpartum

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Carroll University

    Waukesha, Wisconsin, 53186, United States

More trials for these conditions

Other studies related to the condition(s) this trial covers.