Spinal Cord Injury Clinical Trial
Official title:
Southern California Spinal Cord Injury Model System: A Randomized Clinical Trial to Evaluate Two Prevention Programs for Maintenance of Shoulder Health and Function After Spinal Cord Injury
Verified date | April 2018 |
Source | Rancho Research Institute, Inc. |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine if a shoulder exercise program can prevent the onset of shoulder pain and improve community participation in persons who have a spinal cord injury (SCI). Upon entry into the study patients will have pain-free shoulders and will be followed for 3 years to determine rate of shoulder pain development. Patients will learn a simple shoulder home exercise program and will be instructed on techniques to protect their shoulder during wheelchair propulsion, transfers and activities of daily living. Patients will be instructed to perform the home exercise program 3 days per week. Two types of treatment (training) delivery approaches that have been documented to reduce chronic shoulder pain will be compared. The rate of shoulder pain development for the two groups will be compared to the rate of shoulder pain development in the historical control group. The investigators hypothesize that the rate of shoulder pain development will be lower in the experimental treatment groups compared to the historical control group. Any differences between the two treatment delivery approaches for the experimental treatment groups will help to provide guidelines for the most effective delivery approach of a shoulder pain prevention program.
Status | Completed |
Enrollment | 148 |
Est. completion date | July 2017 |
Est. primary completion date | July 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - spinal cord injury - at least 2 years duration post spinal cord injury and no greater than 20 years duration post spinal cord injury - at least 18 years of age - free of shoulder pain that interferes with daily activities or requires medical intervention at the time of enrollment in the study - a total score on the "Wheelchair User's Shoulder Pain Index" of 10 or less - adequate arm strength and movement to perform the shoulder exercise program Exclusion Criteria: - positive shoulder impingement signs (positive Hawkins-Kennedy test and painful arc in shoulder abduction or flexion) - biceps tendonitis (positive Speed's test) - adhesive capsulitis, or cervical radiculopathy - a history of shoulder injury or surgery or orthopedic or neurologic disorders (other than SCI) that would impact arm function |
Country | Name | City | State |
---|---|---|---|
United States | Rancho Los Amigos National Rehabilitaiton Center | Downey | California |
Lead Sponsor | Collaborator |
---|---|
Rancho Research Institute, Inc. | Rancho Los Amigos National Rehabilitation Center |
United States,
Mulroy SJ, Thompson L, Kemp B, Hatchett PP, Newsam CJ, Lupold DG, Haubert LL, Eberly V, Ge TT, Azen SP, Winstein CJ, Gordon J; Physical Therapy Clinical Research Network (PTClinResNet). Strengthening and optimal movements for painful shoulders (STOMPS) in chronic spinal cord injury: a randomized controlled trial. Phys Ther. 2011 Mar;91(3):305-24. doi: 10.2522/ptj.20100182. Epub 2011 Feb 3. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Shoulder torque | Shoulder torque testing will be performed using either a Biodex machine or a handheld dynamometer for the motions of isometric shoulder abduction, adduction, flexion, extension, internal rotation and external rotation. | Baseline, 18 month, and 36 month evaluation time points | |
Other | Self-Efficacy | Patients will complete a questionnaire rating their confidence or self-efficacy in regards to exercise. | Baseline, 18 month and 36 month evaluation time points | |
Other | Community Participation | Patients will asked to complete the questionnaire, "Reintegration To Normal Living Index". | Baseline, 18 month and 36 month evaluation time points | |
Primary | Presence of shoulder pain | Presence of shoulder pain will be measured using the "Wheelchair User's Shoulder Pain Index". This questionnaire uses a visual analog scale to rate level of shoulder pain during the previous week while performing 15 common daily activities such as transferring from the bed to a wheelchair or pushing a wheelchair > 10 minutes. | 36 month (3 year) evaluation time point | |
Secondary | Activity levels | Patients will be called every 2-3 months to report the frequency and intensity of their shoulder exercise program. Patients will be asked questions about their arm use specific to their functional abilities during the previous 1 to 3 days, such as the number of transfers performed, number of depression raises performed, how often they use their arms for chores or use their arms to help with walking (if applicable). All patients with a manual wheelchair will have an odometer installed on their wheelchair and will report their distance and speed of wheelchair propulsion. | Baseline and every 2-3 months over the 3 year study |
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