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Gua Sha Therapy for Chronic Low Back Pain

Gua Sha Therapy for Chronic Low Back Pain: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03333213
Enrollment
50
Registered
2017-11-06
Start date
2009-01-01
Completion date
2010-12-01
Last updated
2017-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Back Pain

Brief summary

Chronic low back pain is a major public health burden with only limited evidence of effectiveness for complementary and traditional therapies. Gua Sha is a traditional East Asian therapy traditionally used in the treatment of spinal pain. This study aimed to test the efficacy of Gua Sha therapy in patients with chronic low back pain A total of 50 patients with chronic low back pain were randomized to either two Gua Sha treatments (n=25) or a waitlist control group (n=25). Primary outcome measure was current pain intensity on a 100-mm visual analog scale; secondary outcome measures included back-related function (Oswestry Disability Index), movement-related pain (modified Pain on Movement Questionnaire), as well as pressure pain threshold, mechanical detection threshold, and vibration detection threshold.

Detailed description

Chronic low back pain is a major public health burden with only limited evidence of effectiveness for complementary and traditional therapies. Gua Sha is a traditional East Asian therapy traditionally used in the treatment of spinal pain. This study aimed to test the efficacy of Gua Sha therapy in patients with chronic low back pain A total of 50 patients with chronic low back pain were randomized to either two Gua Sha treatments (n=25) or a waitlist control group (n=25). Primary outcome measure was current pain intensity on a 100-mm visual analog scale; secondary outcome measures included back-related function (Oswestry Disability Index), movement-related pain (modified Pain on Movement Questionnaire), as well as pressure pain threshold, mechanical detection threshold, and vibration detection threshold.

Interventions

OTHERGua Sha

Sponsors

Universität Duisburg-Essen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* non-specific low back pain at least once weekly for at least the previous 3 months * average back pain intensity hat least 40mm on a 100mm visual analog scale (VAS)

Exclusion criteria

* specific low back pain due to trauma, disc protrusion, whiplash, congenital deformity of the spine, spinal stenosis, neoplasm, inflammatory rheumatic disease, or oncologic disease * 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

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity12 weeks100-mm visual analogue scale (VAS) ranging from 0mm meaning 'no pain at all' to 100mm meaning 'the worst pain imaginable'

Secondary

MeasureTime frameDescription
Functional disability12 weeksOswestry Disability Index (ODI)
Pressure-pain threshold (PPT)12 weeksPPT was measured using a digital algometer (Somedic AB, Horby, Sweden).
Pain on movement12 weeksPain on Movement Questionnaire (POM)
Vibration detection threshold (VDT)12 weeksVDT was determined using a Rydel-Seiffer tuning fork (64 Hz, 8/8 scale)
Adverse events12 weeks
Mechanical detection threshold (MDT)12 weeksMDT was measured with a set of von Frey filaments (Somedic Sales AB, Horby, Sweden).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026