Chronic Low Back Pain Clinical Trial
Official title:
Motor Control Exercise and Patient Education for the Management of Chronic Low Back Pain in a Low-Resource Rural Nigerian Community: A Pilot Randomized Controlled Trial.
Verified date | November 2018 |
Source | Bayero University Kano, Nigeria |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of this pilot single-blind randomized clinical trial is to assess the feasibility of implementing motor control exercise and patient education for the management of chronic low back pain (CLBP) in a low resource rural Nigerian community.
Status | Completed |
Enrollment | 30 |
Est. completion date | May 1, 2018 |
Est. primary completion date | April 30, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Male and female between 18 and 65 years old. - Primary complaint of LBP experienced at least over the previous 3-month duration. - Ability to read/understand English or Hausa language. Exclusion Criteria: - Previous history of thoracic spine or lumbosacral spine surgery. - Any neurological findings indicating radiculopathy. - Evidence of serious spine pathology (e.g. tumor, infection, fracture, spinal stenosis, inflammatory disease). - Unstable or severe disabling chronic cardiovascular and pulmonary disease. - History of serious psychological or psychiatric illness. - Current pregnancy |
Country | Name | City | State |
---|---|---|---|
Nigeria | Tsakuwa Primary Healthcare Center | Kano |
Lead Sponsor | Collaborator |
---|---|
Bayero University Kano, Nigeria |
Nigeria,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in pain Intensity | Pain Intensity will be measured by an 11-point (0-10) Numerical Pain Rating Scale (NPRS). | Baseline and 6 weeks after beginning treatment. | |
Primary | Change in functional disability | Functional disability will be measured by Oswestry disability index (ODI). The questionnaire consists of 10 items with each item having six statements. All scores are summed, then multiplied by two to obtain the index (range 0 to 100) with higher score indicating greater disability. | Baseline and 6 weeks after beginning treatment. | |
Secondary | Patient satisfaction | Patient satisfaction with treatment will be assessed using a 5-point Likert scale ranging from "very dissatisfied" (0) to "very satisfied" (4), with higher scores reflecting greater satisfaction. | 6 weeks after beginning treatment. |
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