Sciatica sufferers: which quick fix works best?
NCT ID NCT07161323
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study compares two hands-on techniques—SNAG (a gentle spinal glide) and sciatic nerve mobilization exercises—for easing non-specific sciatica pain. Thirty adults with pain lasting over 12 weeks will try both methods in a crossover design, with each session separated by 10 days. Researchers will measure changes in disability, range of motion, and function to see which approach offers better short-term relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sustained Natural Apophyseal Glide (SNAG) technique and Sciatic Nerve Mobilization Exercise (SNME)
- What this could lead to
- If successful, this study could show which hands-on technique provides faster relief for sciatica pain, helping guide physical therapy choices.
- What could go wrong
- This is a small, early-stage crossover trial with only 30 participants, so results may not apply to everyone. The effects measured are short-term, and long-term benefits are unknown.
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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Jul 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 50 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Adults between the ages of 20 and 50, * Individuals describing non-specific sciatic pain characterized by unilateral low back pain accompanied by radiating symptoms to the leg, * Duration of pain longer than 12 weeks, * Presence of pain during the Slump Test and Straight Leg Raise Test, * No history of any physical therapy or intervention in the past month. b: Exclusion Criteria: * Individuals diagnosed with herniated disc or spinal stenosis by a physician, * Physician-diagnosed secondary neurological conditions, * History of spinal surgery, * Individuals describing the origin of their pain as the lower back (without leg involvement), * Presence of neurological symptoms (e.g., foot drop, significant muscle weakness), * Serious medical conditions that may affect treatment or outcomes (e.g., cancer, infections, or inflammatory diseases), * Pregnancy or recent childbirth (within the past year), * Use of medications that may affect pain perception or mobility (e.g., opioids), * Inability to comply with the weekly treatment schedule.
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Clam Fizyoterapi Merkezi
RECRUITINGIstanbul, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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