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
NA
50 participants
INTERVENTIONAL
2009-01-01
2010-12-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Gua Sha therapy
Patients' backs were first covered with Tumarol N Balsam. The study physician then applied a round-edged instrument (the inside smooth edged lip of a metal cap) to patients' skin in downward strokes. Patients were treated twice with a 7-day interval.
Gua Sha
Waitlist control group
Treatments in the control group were not regulated but patients were asked to continue their self-directed medical care. They were offered the Gua Sha therapy once the trial was concluded.
No interventions assigned to this group
Interventions
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Gua Sha
Eligibility Criteria
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Inclusion Criteria
* average back pain intensity hat least 40mm on a 100mm visual analog scale (VAS)
Exclusion Criteria
* dystonia
* pregnancy
* invasive treatment of the spine or spinal surgery within the previous 4 weeks
* oral steroids or anticoagulants
* hemophilia or a skin condition in the area to be treated
* started a new treatment for low back pain within the previous month or planning to start a new treatment within the next month
18 Years
75 Years
ALL
No
Sponsors
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Universität Duisburg-Essen
OTHER
Responsible Party
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Holger Cramer
Research Director
Other Identifiers
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08-3594
Identifier Type: -
Identifier Source: org_study_id