Low Back Pain Clinical Trial
Official title:
A Pilot Project to Study the Effect of Four Osteopathic Treatments on Trunk Muscle Firing Patterns and Temporospatial Parameters of Gait in Persons With Chronic Low Back Pain
| Verified date | March 2014 |
| Source | Nova Scotia Health Authority |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Canada: Ethics Review Committee |
| Study type | Observational |
Eighty percent of Canadians experience low back pain (LBP) at some point in their life
(Waddell, 1987), with a point prevalence of up to 30 percent (O'Sullivan, 2005; Waddell,
1987). Low back pain has severe economic ramifications. Most incidents of low back pain
occur during the prime working years of life, with an estimated cost to the economy at
$14,744 Canadian dollars per person per year (Health Canada, 1998). Indirect costs in the
form of long-term disability were highest for disorders of arthritis and chronic back pain
(Health Canada, 1998). It has been estimated that 12 percent of patients will experience
disability within one year after their first episode of low back pain (Banner, 2006).
Evidence based diagnosis and treatment is important for desirable outcomes.
The investigators predict that there will be changes in A) trunk muscle electromyographic
patterns and in temporo-spatial gait patterns following osteopathic treatment.
| Status | Completed |
| Enrollment | 10 |
| Est. completion date | December 2012 |
| Est. primary completion date | December 2012 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 19 Years to 55 Years |
| Eligibility |
Inclusion Criteria: - between the age of 19 and 55 years old, - able to walk without assistance and /or assistive devices at least 4.7 meters. - have adequate hearing acuity to detect verbal instructions. - have adequate visual acuity to walk safely in usual ambient lighting without holding onto objects. - be able to speak and comprehend English, - have sufficient cognitive ability to follow instructions, and to provide informed consent, as defined by a Mini Mental Status Examination score of greater than 23 out of 30, performed by the research coordinator. Exclusion Criteria: - have had neurological signs and symptoms, or complications such as tumor or infection. - are active in a claim pertaining to a motor vehicle accident or work injury or under any litigation for their pain. - have had previous osteopathic treatment in the last year. - had more than one abdominal surgery, or spinal fracture, or structural deformity such as scoliosis or spondylolithesis (Hubley-Kozey, 2002) - have severe cardiopulmonary disease as determined by a health questionnaire with symptoms such as shortness of breath or chest pain on mild exertion or at rest, - history of severe neurological disorder that impairs balance and mobility eg stroke, Parkinson's disease, peripheral neuropathy - have pain that leads to severe discomfort with minimal movement, - have significant musculoskeletal impairment e.g. arthritis that leads to severe discomfort with walking that could lead to an abnormal gait, - have cognitive compromise impairing ability to care for oneself, and ability to provide informed consent, - have dizziness while standing, - have a history of falls in previous month that might make it unsafe to participate in a gait study |
Observational Model: Cohort, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Canada | CDHA Pain Management Unit | Halifax | Nova Scotia |
| Lead Sponsor | Collaborator |
|---|---|
| Mary Lynch |
Canada,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Two primary outcome measures will be used for this study. The GAITRite gait analysis system and surface electromyography (EMG) respectively. | 12 hours | No |
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