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| Name | Class |
|---|---|
| Massachusetts General Hospital | OTHER |
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The purpose of the study is to investigate whether Gua sha is an effective modality for relieving chronic low back pain specifically in the aged population by comparing the baseline measures of pain intensity, self-perceived disability, back range of motion, back local muscle stiffness, depression, sleeping quality, quality of life, biomarkers measurement, and analgesic intake on days 1 and 7 after a single session of Gua sha treatment. In addition, the investigators are going to compare between Gua sha and hot pack treatments for the above parameters.
Subjects will be randomized to receive firstly either one of the treatment arms, and then crossed over to receive another arm after 30 days washing out period. It is expected that Gua sha is 1) effective in reducing the intensity of chronic low back pain in the elderly; 2) effective in helping one or more outcome measures in this study and 3) more effective on relieving the low back pain than hot pack in terms of the outcome measures in this study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Gua sha | Experimental | Paritcipants in this group will receive a single treatment of Gua sha conducted by a well-trained nurse or Chinese practitioner |
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| Hot Pack Therapy | Active Comparator | Participants in this group will receive a single treatment of Hot Pack conducted by a well-trained nurse or Physiotherapist |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Gua sha | Other | A smooth, rounded-edged Gua sha tool will be press-stroked into the flesh enough to contact the fascial layer start at the midline of the subject's back. A stroke line is typically 4 to 6 inches long. Press-stroking will be repeated in one direction until the petechiae raises on that stroke line, typically 8 to 12 strokes. Gua sha will then be continued at the next stroke line directly adjacent to the one before, until the area covered the lower one third of the back. |
| Measure | Description | Time Frame |
|---|---|---|
| Pain intensity | Visual Analog Scale (VAS) | Day 0 before treatment, Day 1 and day 7 after treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Back range of motion | By using inclinometer | Day 0 before treatment, Day 1 and day 7 after treatment |
| Biomarkers for inflammation and anti-inflammation | Saliva specimen is collected from each subject for measuring the levels of Tumor |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| John Yuen, PhD | The Hong Kong Polytechnic University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| School of Nursing, The Hong Kong Polytechnic University | Kowloon | Hong Kong |
| ID | Term |
|---|---|
| D001416 | Back Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| Hot pack | Other | A hydrocollator pack will be used and it will be stored at 42-43oC in the hydrocollator. 6 layers of towel will be used to cover the hydrocollator pack when applying to the back of the subjects. |
|
| Day 0 before treatment, day 7 after treatment |
| Self-perceived disability | Roland-Morris Disability Questionnaire (RMDQ) | Day 0 before treatment, Day 1 and day 7 after treatment |
| Depression level | Geriatric Depression Scale (GDS) | Day 0 before treatment, Day 1 and day 7 after treatment |
| Sleeping quality | Pittsburgh Sleep Quality index (PSQI) | Day 0 before treatment, Day 1 and day 7 after treatment |
| Quality of life | Short-Form (12) Questionnaire (SF-12) | Day 0 before treatment, day 7 after treatment |
| Record for oral intake of NSAIDs and analgesic drugs | Record | Day 0 before treatment, day 7 after treatment |