Spinal crack or brain hack? how a Back-Popping maneuver may rewire pain circuits
NCT ID NCT07728149
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This trial tests whether a hands-on spinal manipulation technique, called lever positioning manipulation, can ease the leg and back pain caused by a herniated disc. About 84 adults with a herniated disc will receive either the real manipulation or a sham version three times a week for 12 weeks. Researchers will also use brain scans to see if the treatment changes brain networks linked to pain. The goal is to understand not just whether the technique works, but how it might affect the brain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a spinal manipulation technique called lever positioning manipulation
- What this could lead to
- If it works, this could reveal how spinal manipulation changes the brain to relieve pain, pointing toward more targeted treatments for disc-related back and leg pain.
- What could go wrong
- This is an early-stage trial with a sham comparison, so the real effect may be small or no better than placebo. The brain-scan findings are exploratory and may not lead to clear conclusions.
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 126 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 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 to 65 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: Patients with lumbar disc herniation (LDH): * Diagnosis of LDH based on clinical symptoms, physical examination findings, and lumbar imaging consistent with neurological localization; central, paracentral, far-lateral, foraminal, or subarticular lumbar disc protrusion. * Aged 18-65 years, of either sex, and right-handed. * In the non-acute phase of LDH, with symptom duration of more than 2 weeks. * Visual Analog Scale (VAS) score greater than 4 and Japanese Orthopaedic Association (JOA) score less than 15. * No use of analgesics, neurotrophic drugs, or sedatives within 1 month before enrollment. * No systematic treatment, spinal manipulation, or other physical therapies within 1 month before enrollment. * Able to understand the study procedures and complete clinical assessments and MRI scans. * Provides written informed consent. Healthy controls: * Aged 18-65 years, of either sex, and right-handed. * No history of LDH or chronic low back pain. * No current pain condition requiring treatment. * No neurological or psychiatric disorders. * No known structural brain abnormalities. * No MRI contraindications. * Able to complete clinical assessments and MRI scans. * Provides written informed consent. Exclusion Criteria: Patients with LDH: * Low back pain or sciatica caused by conditions other than LDH. * Lumbar spondylolisthesis, lumbar tumor, spinal tuberculosis, severe osteoporosis, or localized lumbar skin lesions that may interfere with treatment. * Severe cardiovascular, cerebrovascular, hepatic, renal, hematopoietic, neurological, or psychiatric disease. * History of severe head trauma, loss of consciousness, or known structural brain abnormality. * Impaired consciousness, severe visual or hearing impairment, speech disorder, or inability to complete clinical assessments. * Non-MRI-compatible metal implants, implanted electronic devices, cardiac pacemakers, severe claustrophobia, or inability to tolerate MRI scanning. * Asymptomatic LDH. * Pregnancy, lactation, or planned pregnancy during the study period. * Participation in another clinical trial within the previous 3 months. * Any condition judged by the investigators to make the patient unsuitable for participation. Healthy controls: * Any condition that may affect eligibility, MRI safety, or data quality.
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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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The Third Affiliated Hospital of Zhejiang Chinese Medical University
Hangzhou, Zhejiang, 310053, China
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