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Randomized clinical trial to compare the effectiveness and safety of double (traditional) versus single (Asian) cupping techniques in chronic low back pain.
Chronic Low Back Pain is a very common pain disorder in the primary care. As in many chronic pain conditions, patients are usually asking for alternative options, especially local traditional and therapies including wet cupping, to replace the long-term use of painkillers. The majority of the wet cupping trials conducted abroad used different techniques, which is different from our local traditional wet cupping technique. This study can identify the technique that is more efficacious in reducing pain, prolonging the pain relieve period, and decrease patient dependence on painkillers in chronic low back pain.The aim of this study is to compare the effectiveness and safety of double (traditional) versus single (Asian) cupping techniques in chronic low back pain. This a randomized comparative effectiveness pilot clinical trial. After taking written informed consent, patient with chronic low back pain will be randomized into two groups, one group to receive wet cupping therapy with the Traditional double technique, the other group to receive it with the Asian single technique. Numeric Rating Scale, Present Pain Intensity and Oswestry Disability Questionnaire will be used to measure the outcome before and after the intervention, one week after the intervention, then two weeks after. Wilcoxon rank sum test for the continuous dependent data analysis and the analysis of covariance ANCOVA, to compare both groups mean scores will be used. The outcome baseline for each score will be used as the covariate. Chi square or Fisher's exact test will be used to compare categorical data with Minimal Clinical Improvement Difference within and between the two groups.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| wet cupping : double cupping | Experimental | wet cupping: (traditional cupping technique): cupping (suction) - Scarification - cupping (suction) |
|
| wet cupping: single cupping | Experimental | wet cupping:(Asian cupping): Puncture by needles then cupping (suction): |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| wet cupping | Procedure | In double cupping (traditional technique): Cupping (suction) then scarification then cupping (suction). In single cupping (Asian): puncture using auto lancet then cupping (suction). In both techniques 4 out of 6 acupoints (BL23, BL24, BL25 bilateral) will be selected. |
| Measure | Description | Time Frame |
|---|---|---|
| Pain Numeric rating scale (NRS) before and after intervention | numeric pain scale to be measured before intervention then two weeks after | 14 DAYS |
| Measure | Description | Time Frame |
|---|---|---|
| pain: McGill, Persistent Pain Intensity (PPI) | before intervention and two weeks later | 14 days |
| functioning (Disability) using the Oswestry Disability Questionnaire (ODQ) | functionality will be measured using the questionnaire and compared two weeks after intervention |
| Measure | Description | Time Frame |
|---|---|---|
| Patient satisfaction using the Integrative Medicine Patient Satisfaction Scale (IMPSS) | 5 grade scales will be compared to a five grade scales of expectation measured before intervention | up to 14 days |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Sulaiman AlEidi, MBBS | NCCAM , MOH, Riyadh, Saudi Arabia | Principal Investigator |
| Mohamed Khalil, MD | NCCAM.MOH | Study Chair |
| Ashry Gad Mohamed, MD | King Saud University | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| King Fahad Hospital | Jeddah | Jeddah | Saudi Arabia | |||
| King Fahad Hospital |
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| ID | Term |
|---|---|
| D017116 | Low Back Pain |
| ID | Term |
|---|---|
| D001416 | Back Pain |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
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|
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| 14 days |
| the Safety of the two wet cupping techniques, by collecting safety data after two weeks of the intervention | using the WHO guidelines for classification of adverse events | up to 14 days |
| Madinah |
| Madinah |
| Saudi Arabia |
| D013568 |
| Pathological Conditions, Signs and Symptoms |