Biomechanics of Wheelchair Transfers
This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT00645567
First received: March 19, 2008
Last updated: January 28, 2013
Last verified: January 2013
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Purpose
This is a laboratory-based study to evaluate the risk of shoulder injury associated with transfers between wheelchair and vehicle in persons with spinal cord injury. Four new devices will be compared against an unassisted transfer.
| Condition |
|---|
|
Spinal Cord Injury |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Crossover Time Perspective: Cross-Sectional |
| Official Title: | Evaluation of Transfer Technologies to Preserve Shoulder Function in SCI |
Resource links provided by NLM:
Further study details as provided by Department of Veterans Affairs:
Primary Outcome Measures:
- Shoulder kinematics & kinetics [ Time Frame: Calculated during task performance for each of the 5 devices tested ] [ Designated as safety issue: No ]
| Enrollment: | 5 |
| Study Start Date: | January 2010 |
| Study Completion Date: | December 2012 |
| Primary Completion Date: | March 2011 (Final data collection date for primary outcome measure) |
| Groups/Cohorts |
|---|
| Group 1 |
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Probability Sample |
Study Population
A sample of 58 veterans with paraplegia who use a rigid manual wheelchair will be recruited to participate in this study.
Criteria
Inclusion Criteria:
- level of SCI will be limited to ASIA A classification at T2 through L5 level to standardize physical capabilities,
- SCI for at least 2 years (neurologically stable,
- use rigid manual wheelchair as a primary means of mobility,
- able to self-propel wheelchair,
- able to independently transfer between wheelchair and vehicle,
- between the ages of 18-65,
- living in the community within 100 miles of the Tampa VA hospital,
- able to follow simple instructions,
- free from acute upper extremity injury for at least six months (determined by chart review) to minimize risk of injury during task performance,
- comparable bilateral functional range of motion and strength of the shoulders, elbows and wrists (determined by physical evaluation) to minimize risk of injury during task performance.
Exclusion Criteria:
Candidates who present:
- progressive disease (e.g. spinal tumor),
- extended bedrest for more than 30 days,
- ventilator-dependent,
- any cardiac or respiratory condition that would limit subject's physical performance,
- unstable medical conditions,
- use of power wheelchair or scooter as primary means of mobility,
- pregnancy,
- clinical evidence of severe musculoskeletal disorders of the upper extremity will be precluded from participating in this study.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00645567
Locations
| United States, Florida | |
| James A. Haley Veterans Hospital | |
| Tampa, Florida, United States, 33612-4745 | |
Sponsors and Collaborators
Investigators
| Principal Investigator: | John D. Lloyd, PhD BS | James A. Haley Veterans Hospital |
More Information
No publications provided
| Responsible Party: | Department of Veterans Affairs |
| ClinicalTrials.gov Identifier: | NCT00645567 History of Changes |
| Other Study ID Numbers: | B6103-R |
| Study First Received: | March 19, 2008 |
| Last Updated: | January 28, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by Department of Veterans Affairs:
|
Biomechanics Ergonomics Spinal Cord Injury Pain Shoulder |
Additional relevant MeSH terms:
|
Spinal Cord Injuries Spinal Cord Diseases Central Nervous System Diseases |
Nervous System Diseases Trauma, Nervous System Wounds and Injuries |
ClinicalTrials.gov processed this record on June 18, 2013