Can simple exercises prevent postpartum pelvic problems?
NCT ID NCT03247660
First seen Aug 25, 2026 · Last updated Aug 26, 2026 · Updated 1 time
Summary
This trial tests whether pelvic floor muscle training, hypopressive exercises, or pelvic health education can prevent or treat pelvic floor dysfunction in first-time mothers after vaginal delivery. Participants, enrolled 6-8 weeks postpartum, will be randomly assigned to one of these approaches. The study measures changes in symptoms and quality of life using validated questionnaires, aiming to identify the most effective non-surgical strategy for postpartum recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pelvic floor muscle training, hypopressive exercises, and pelvic health education
- What this could lead to
- If effective, these non-invasive approaches could offer new mothers a simple way to prevent or ease pelvic floor problems after childbirth, improving quality of life.
- What could go wrong
- This is a relatively small trial, and results may not apply to all women. The exercises require consistent practice, and individual outcomes can vary.
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
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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
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165 people
The number who actually took part.
- Started
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Oct 2017
- Finished
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Dec 2024
- Lead sponsor
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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
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18 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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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 Hide 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: * Postnatal women (6 and 8 weeks after vaginal delivery) * Primiparous * Whose vaginal delivery has occurred in the "Príncipe de Asturias" Hospital * Women have not been already treated for pelvic floor dysfunction * Women reading, understanding and freely signing an informed consent form Exclusion Criteria: * Postnatal women with medical diagnosis of pelvic floor dysfunction (PFD) prior to pregnancy and delivery * Women with a history of conservative treatment or PFD surgery * Women with concomitant or systemic disease that may affect the treatment (neurological, gynecological, urological or connective tissue), or with active or recurrent urinary infection without treatment at the time of the intervention proposed in this study, or hematuria. * Women with perineal pain preventing vaginal dynamometry. * Postnatal women with cognitive impairment or insufficient Spanish-language proficiency preventing adequate understanding of study procedures. * Women with severe maternal complications or serious neonatal conditions.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Alcalá. FPSM research group. HUPA
Alcalá de Henares, Madrid, 28805, Spain
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