Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
195 participants
OBSERVATIONAL
2013-01-31
2014-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Low back pain subjects
Subjects with chronic or recurrent low back pain
StromaGlide
No low back pain subjects
Subjects who are generally healthy with no low back pain
StromaGlide
Interventions
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StromaGlide
Eligibility Criteria
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Inclusion Criteria
* able to read and understand English
* able to understand and sign a consent form
* history of recurrent or chronic low back pain
* no history of low back pain or other chronic pain that has limited activities of daily living or work
* numerical chronic pain index of less than 0.5
Exclusion Criteria
* major structural spinal deformity (scoliosis, kyphosis, stenosis)
* ankylosing spondylitis or rheumatoid arthritis
* neurological deficit (weakness or sensory loss, decreased deep tendon reflexes suggesting nerve root compression, but not subjective symptoms of nerve root irritation (sciatica))
* radicular pain
* neurological or major psychiatric disorder
* bleeding disorders
* corticosteroid or anticoagulant medication
* substance abuse
* pregnancy
* active worker's compensation or disability case
* in litigation for a low back pain problem
* acute systemic infection
18 Years
ALL
Yes
Sponsors
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National Center for Complementary and Integrative Health (NCCIH)
NIH
Stromatec, Inc.
INDUSTRY
Responsible Party
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Robert Davis
Principal Investigator
Locations
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Stromatec, Inc
Burlington, Vermont, United States
Countries
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Other Identifiers
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