Pregnancy pain relief: simple exercise program shows promise
NCT ID NCT07186504
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tests whether a weekly exercise class, combined with pelvic floor therapy when needed, can reduce pelvic girdle pain in pregnant women. Forty women with pelvic pain will be randomly assigned to either the exercise program or standard prenatal care. Researchers will measure pain levels and daily function before, during, and after pregnancy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- adapted physical activity and pelvic floor rehabilitation
- What this could lead to
- If it works, this could offer a safe, drug-free way to reduce pelvic pain and improve daily function for pregnant women.
- What could go wrong
- This is a small, early exploratory trial with only 40 participants, so results may not apply to all women. The intervention is time-intensive and may not be widely adopted.
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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About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2025
An estimate. Start dates often move.
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- 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 years and older
- 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: * Pregnant women aged ≥18 years * Gestational age ≤27 weeks at enrollment * Clinically confirmed pelvic girdle pain, defined as: * Pain localized between the posterior iliac crest and the gluteal fold, particularly around the sacroiliac joints and/or pubic symphysis, Pain intensity ≥3/10 on Visual Analog Scale (VAS), At least 3 positive clinical tests among: Posterior Pelvic Pain Provocation (P4) test, Patrick's FABER, Menell's test, Active Straight Leg Raise (ASLR), and palpation of long dorsal sacroiliac ligament or symphysis pubis * Ability to understand and provide written informed consent Exclusion Criteria: * Isolated low back pain without pelvic involvement * Contraindications to exercise during pregnancy (e.g., severe preeclampsia, placenta previa after 26 weeks, risk of preterm labor, ruptured membranes, significant cardiac or pulmonary disease) * Neurological, rheumatologic, or orthopedic conditions that may interfere with participation * Insufficient French language proficiency to understand questionnaires and instructions * Participation in another interventional study that could affect outcomes
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
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