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Which postpartum exercise is best for pelvic floor health? new trial aims to find out

NCT ID NCT07313683

Disease control Sponsor: University of Alcala 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 This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study will compare two exercise programs—lumbopelvic stabilization exercises and hypopressive exercises—in 84 women who had a vaginal delivery 6 to 12 weeks earlier. The goal is to see which approach is safer and more effective for improving pelvic floor recovery and helping women return to daily activities, work, and sports. Participants will attend weekly sessions over 8 weeks, and researchers will measure quality of life, sexual function, and other outcomes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
exercise programs (lumbopelvic stabilization exercises or hypopressive exercises)
What this could lead to
If successful, this could provide clear guidance on which exercise approach is safer and more effective for postpartum pelvic floor recovery, helping women return to daily activities and sports with less risk of long-term pelvic floor disorders.
What could go wrong
This is a small, early-stage trial (84 participants) comparing two exercise methods, so results may not apply to all women. The study hasn't started recruiting yet, and the benefits may be modest or not significantly different between groups.

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 84 people

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

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Feb 2029

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

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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 * Primiparous or multiparous women with an uncomplicated vaginal delivery. * Women between 6 and 12 weeks postpartum. * Women who have freely read, understood, and signed the informed consent form. Exclusion Criteria * Cesarean delivery. * Pelvic or perineal pain greater than 4/10 during physical examination. * Clinical diagnosis of pelvic floor myofascial pain syndrome. * Evidence of levator ani muscle avulsion. * Third- or fourth-degree perineal tears. * History of pelvic surgery. * History of pelvic fractures and/or pelvic neoplasms. * Current pregnancy. * Neurological disorders. * Active vaginal or urinary tract infections. * Cognitive, auditory, or visual impairments that limit comprehension, questionnaire completion, consent, or participation in the study. * Individuals under 18 years of age.

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Conditions

The condition(s) this trial relates to.

Pelvic Floor Disorders

As listed by the trial registrant

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

Pelvic floor disorders Postpartum period

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

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    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

  • Faculty of Nursing and Physiotherapy, University of Alcalá

    Alcalá de Henares, Madrid, 28805, Spain

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