Can sling exercises rewire back pain? trial tests muscle control in sciatica

NCT ID NCT06558383

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Not yet recruiting
Registered, but not yet taking participants.
By invitation only
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
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The trial has finished. Results may not be published yet.
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Cancelled before anyone took part.

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First seen Sep 16, 2026 · Last updated Sep 17, 2026 · Updated 1 time

Summary

Researchers at Cairo University are studying whether a specific exercise program that targets the posterior oblique sling, a network of muscles in the lower back and pelvis, can improve muscle coordination and function in people with lumbosacral radiculopathy. This condition causes leg pain from a pinched nerve in the lower spine. The trial enrolls 40 adults with chronic L5/S1 disc herniation and moderate to severe leg pain. Participants receive either the sling activation program or a standard physical therapy program, both for 18 sessions over six weeks. The study measures muscle activity, pelvic motion, pain thresholds, and disability to see if the targeted exercises lead to better outcomes.

What this could mean

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

Active substance
a targeted exercise program that activates the posterior oblique sling, a group of muscles connecting the back, pelvis, and leg
What this could lead to
If it works, this could offer a non-drug way to improve movement and reduce disability for people with nerve-related low back and leg pain.
What could go wrong
The trial is small and early, so results may not hold for everyone. Exercise programs can cause temporary soreness, and some participants may not improve.

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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

40 people

The number who actually took part.

Started

Sep 2024

Finished

Oct 2025

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

30 to 46 years

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: * Age ranges from 30 to 46 * L5/S1 disc herniation. * Duration of pain is more than three months. * body mass index less than 30 kg/cm2 * ability to perform prone hip extension task with no pain * impaired lumbopelvic stability (\<5 mmHg pressure difference from baseline to end prone hip extension task) * moderate to severe lumbosacral radicular pain Exclusion Criteria: * Red flags: spinal tumors, cauda equina syndrome, spinal fractures, osteoporosis, infection. * Bilateral symptoms. * Spondylolisthesis, spondylitis, and spinal canal stenosis. * Previous lumbopelvic or hip surgery or injection * Any hip structural abnormality such as malformations, impingements and degeneration. * Postural deviations such as scoliosis, kyphosis, lateral shift. * True leg length discrepancy. * Pregnancy and Gynecological problems.

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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.

Contacts and locations

Locations

  • faculty of physical therapy Cairo university

    Giza, Egypt

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