A targeted exercise and therapy plan may help new mothers beat back pain
NCT ID NCT07790848
First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time
Summary
This trial tests whether a structured physiotherapy program can reduce low back pain and improve function in women who gave birth within the last six months. The program combines core exercises, pelvic floor training, manual therapy, posture correction, and ergonomic advice over six weeks. Researchers will compare it with routine postpartum care in 40 women, measuring pain, disability, core endurance, fatigue, and quality of life. The goal is to see if this approach can become a standard part of maternal healthcare in Pakistan.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Multimodal physiotherapy program including core stabilization exercises, pelvic floor training, manual therapy, posture correction, ergonomic education, and home exercise guidance
- What this could lead to
- If it works, this could support adding physiotherapy to routine postpartum care in Pakistan, helping new mothers recover from low back pain and regain daily function.
- What could go wrong
- This is a small early trial with 40 participants, so results may not apply broadly. The program requires six weeks of supervised sessions, and some women may not complete it.
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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 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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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20 to 40 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: * Within six months postpartum following vaginal or caesarean delivery. * Experiencing low back pain or lumbopelvic pain after childbirth. * Pain intensity ≥3 on the Numeric Pain Rating Scale during activity or rest. * Able to attend supervised physiotherapy sessions for six consecutive weeks. * Willing to provide informed consent and participate in follow-up assessments. Exclusion Criteria: * History of spinal surgery or diagnosed structural spinal deformities such as scoliosis, spondylolisthesis, or disc herniation. * Severe postpartum complications including postpartum haemorrhage, infection, or wound dehiscence limiting physical activity. * Pelvic organ prolapse grade II or above or severe pelvic floor dysfunction requiring specialized care. * Uncontrolled systemic illness such as diabetes mellitus, hypertension, or thyroid dysfunction affecting exercise tolerance. * Current participation in another structured physiotherapy or rehabilitation program for low back pain. * Neurological disorders or musculoskeletal conditions unrelated to postpartum low back pain that may affect outcomes.
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As listed by the trial registrant
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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
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