NCT Number: NCT03333213
Gua Sha Therapy for Chronic Low Back Pain
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.
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Conditions
Age range
18 year–75 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
About this study
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.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
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
Treatment and study plan
Primary outcomes
-
Pain intensity
Time frame: 12 weeks
100-mm visual analogue scale (VAS) ranging from 0mm meaning 'no pain at all' to 100mm meaning 'the worst pain imaginable'
Secondary outcomes
-
Pain on movement
Time frame: 12 weeks
Pain on Movement Questionnaire (POM)
-
Functional disability
Time frame: 12 weeks
Oswestry Disability Index (ODI)
-
Pressure-pain threshold (PPT)
Time frame: 12 weeks
PPT was measured using a digital algometer (Somedic AB, Horby, Sweden).
-
Mechanical detection threshold (MDT)
Time frame: 12 weeks
MDT was measured with a set of von Frey filaments (Somedic Sales AB, Horby, Sweden).
-
Vibration detection threshold (VDT)
Time frame: 12 weeks
VDT was determined using a Rydel-Seiffer tuning fork (64 Hz, 8/8 scale)
-
Adverse events
Time frame: 12 weeks
Sponsors and collaborators
Lead sponsor
Universität Duisburg-Essen
Other
Registry information
Official study title
Gua Sha Therapy for Chronic Low Back Pain: a Randomized Controlled Trial
Important dates
- Study start
- 2009
- Primary completion
- 2010
- Study completion
- 2010
- First posted
- Nov 6, 2017
- Registry last updated
- Nov 6, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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