Manual Therapy for the Treatment of Shoulder Pain for Overuse Syndrome Wheelchair Dependent Persons
NCT ID: NCT04991415
Last Updated: 2021-08-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
12 participants
INTERVENTIONAL
2014-12-31
2021-07-31
Brief Summary
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Detailed Description
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In the able bodied population, the most common recommendation for overuse syndrome is resting the affected joint. In persons with paraplegia and wheelchair dependence, this recommendation is unrealistic and would lead to non-use of the person's primary means of mobility (the wheelchair). Often, patients require pharmacologic intervention to help alleviate the pain in order to participate in therapy sessions and activities of daily living. Current treatment options for overuse syndrome include oral medication including narcotic pain medication and anti-inflammatory medication, modalities, injections, and surgery. Despite these treatment options, pain from overuse syndrome remains a prevalent problem with no treatment option proven superior and no gold standard of treatment identified. An alternative treatment for shoulder pain with evidence to support efficacy in the able bodied population is Manual Therapy (MT). Unfortunately, there have been no prior research studies published examining the therapeutic efficacy of MT for overuse injuries of the shoulder in patients with paraplegia. This study will determine if MT, is efficacious to reduce pain in this population. A total of 20 patients with paraplegia identified in the outpatient clinic at Craig Hospital with overuse syndrome of the shoulder will be enrolled in the study. Ten of the participants will be randomized to the control group and receive no MT and ten participants will be randomized to the treatment group and receive MT for three days per week x 2weeks. The treatment will be provided by a Doctor of Osteopathic Medicine (D.O.), physical, or occupational therapists trained to perform MT. During this study, the subject's pain and function will be measured by a 10 point questionnaire, the Numeric Pain Rating Scale (NPRS) and the Wheelchair Users Shoulder Pain Index (WUSPI). The NPRS and WUSPI are included in Appendix 1 and 2. The NPRS has been validated as a ratio scale for pain. The WUSPI has been validated as a scale for assessment of baseline shoulder dysfunction and for periodic measurement in longitudinal studies of musculoskeletal complications in wheelchair users. Data gathered from these outcome measures will be accumulated and statistically analyzed to examine the potential benefit of MT in the target population. This investigation will be one of the first to examine the relationship between MT and reduction in shoulder pain for treatment of overuse syndrome in persons with paraplegia. It will also examine if decreased pain secondary to MT will result in a decrease in pain during functional activity in these individuals. The results of this pilot study may result in publication in peer reviewed journals, presentations at national symposiums and application for funding for Complementary Medicine grant by the National Institute of Health or other available grant for larger study.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Treatment
30 minutes of manual therapy three times a week for two weeks (six total sessions).
Manual Therapy
Control
No intervention
No interventions assigned to this group
Interventions
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Manual Therapy
Eligibility Criteria
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Inclusion Criteria
* Spinal cord injury, non-ambulatory, wheelchair user,
* Pain in shoulder from overuse injury,
* Pain interference on the WUSPI of at least 6/10 on at least 2 of the transfer items and any one of the remaining items,
* English-speaking,
* Stable spine,
* Full weight-bearing status in bilateral upper extremities (i.e. no orthopedic precautions on UE weight-bearing activities)
* Greater than 3 months post initial spinal cord injury
* Diagnosis of overuse syndrome of the shoulder
Exclusion Criteria
* Fractures in upper limbs.
* Concurrent diagnosis of Fibromyalgia.
* Cervical radiculopathy.
* Previous shoulder pathology
* Neuromuscular junction disorders (such as myasthenia gravis),
* Psychiatric disorder.
* Lack capacity to provide informed consent.
18 Years
65 Years
ALL
No
Sponsors
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Craig Hospital
OTHER
Responsible Party
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Jennifer Coker
Research Scientist I
Principal Investigators
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Jeffrey Berliner, DO
Role: PRINCIPAL_INVESTIGATOR
Physician, Director of Outpatient Medicine
Locations
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Craig Hospital
Englewood, Colorado, United States
Countries
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Other Identifiers
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Manual Therapy
Identifier Type: -
Identifier Source: org_study_id
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