Mind over back pain: expectations may boost spinal manipulation results
NCT ID NCT07507604
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looks at whether watching someone else's positive or negative experience with spinal manipulation can change pain relief and inflammation in people with chronic low back pain. About 73 adults will be randomly assigned to see a positive, neutral, or negative example before receiving the same spinal adjustment. Researchers will measure pain, disability, and blood markers of inflammation before and after treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- spinal joint manipulation
- What this could lead to
- If it works, this could show that a patient's expectations before treatment can boost pain relief from spinal manipulation.
- What could go wrong
- This is a small, early-stage study with only 73 participants, so results may not apply to everyone. The effect of expectations may be small or hard to measure.
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 73 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Sep 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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18 to 65 years
- Sex
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Anyone
- 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: * people with low back pain lasting longer than 3 months, aged 18 to 65 years, * highest reported pain intensity during the last 24 hours of at least 4 out of 10 on the 11-point Numeric Pain Rating Scale (NPRS-11), where 0 = no pain and 10 = worst imaginable pain, * clinical diagnosis of chronic non-specific low back pain (NSCLBP) based on symptoms located in the lumbar spine region and not on imaging findings, * no use of nonsteroidal anti-inflammatory drugs (NSAIDs) for at least 7 days before the study, * no use of pain medication for at least 24 hours before the study, * no use of corticosteroids, * no previous spinal manipulation therapy, * no alcohol, nicotine, or coffee consumption for at least 12 hours before the study, * written informed consent to participate in the study. Exclusion Criteria: * physiotherapy students, * presence of red flags, such as a history of cancer, constant or non-mechanical pain, progressive or radiating pain, sensory deficits in the trunk or - lower limbs, lower limb muscle weakness, or bladder/bowel dysfunction, * body mass index (BMI) greater than 30, * previous lumbar spine surgery, * lumbar spine injury within 6 months before the study, * diagnosed diabetes, * diagnosed rheumatic diseases, * affective disorders such as post-traumatic stress disorder (PTSD) or schizophrenia, * spondylolisthesis or spondylolysis confirmed by imaging, * diagnosed endometriosis, * use of hormonal medications, * sleep disorders, * shift work, * musculoskeletal injury within the last 14 days, * active infection, * pregnancy, * endocrine disorders such as hyperthyroidism or hypothyroidism, * use of opioid medications, including over-the-counter combination products such as codeine with paracetamol, * current or recent use of antidepressants affecting serotonin or dopamine (including SSRIs, SNRIs, tricyclic antidepressants, MAO inhibitors, or ketamine), * current diagnosis of major depressive disorder or bipolar disorder, as well as PTSD or schizophrenia, * ongoing psychotherapy during the study period, * cognitive impairment or significant hearing impairment that may interfere with understanding or processing the observational learning procedure.
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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
2 sites. 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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John Paul II University in Biała Podlaska
RECRUITINGBiała Podlaska, Lublin Voivodeship, 21-500, Poland
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Laboratory of the John Paul II University in Biała Podlaska
RECRUITINGBiała Podlaska, Lublin Voivodeship, 21-500, Poland
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