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| Name | Class |
|---|---|
| DePuy Spine | INDUSTRY |
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The goal of this study is to evaluate children and adolescents with idiopathic scoliosis who are undergoing spinal fusion using motion analysis, balance, and outcome questionnaires. Little research has been done to evaluate how different fusion levels impact walking patterns, range of motion, posture and balance following spine instrumentation in children with idiopathic scoliosis. Debate still continues whether posterior spinal instrumentation with the last instrumented vertebra at or above Lumbar 3 (L3) will provide sufficient spine correction, greater motion, and better posture and balance when compared to a child with instrumentation at Lumbar 4 (L4). Furthermore, how does the spine fusion endpoint (last instrumented vertebra) impact quality of life, participation, and impairment in children and adolescents with idiopathic scoliosis and how do they compare to healthy age-matched peers. The goal of this study is to compare these two end points using gait analysis, postural stability, and outcome tools with the hopes of providing better clinical care to children with idiopathic scoliosis.
The study population will include sixty (60) children with idiopathic scoliosis who will undergo spine surgery and sixty (60) developing children "Control Group". Scoliosis patients will undergo a period of testing which requires three visits: pre-operative evaluation, one-year post-operative evaluation, and two-year post-operative evaluation. The Control Group will require one initial assessment. A total of 240 evaluations will be performed over a three-year period. We will evaluate the correlation among outcome tools and quantitative measures in order to determine how these instruments can be used more effectively for better treatment. Subjects and their parents will be fully informed of the nature of the study as well as the potential risk involved and sign the appropriate consent form. The study will be reviewed by the IRB and include HIPAA compliance. This will be accomplished during testing at the Shriners Hospital for Children- Chicago Motion Analysis Lab. All possible steps will be taken to assure the safety and convenience of the study participants. All subjects will be evaluated using clinical outcome tools (PODCI, SF-36) and will undergo quantitative 3-D motion analysis and postural stability assessment. Quantitative 3-D gait analysis will be done with our 14-camera Motion Capture system and passive reflective markers (Figure 3). Motion analysis will be performed with each subject walking at a comfortable and natural speed on the laboratory walkway. Passive markers will be attached to anatomic landmarks in standardized locations using double-backed tape. Marker coordinate data will be used to determine range of motion and joint angles.
Four forceplates will be used to measure kinetic data and static balance. Postural stability testing will be performed on all subjects (Figure 4). We will evaluate responses to dynamic stability challenges that investigates motor and sensory control and adaptation to perturbations. Static (quiet standing) postural stability tests will be done on all subjects. A licensed physical therapist (PT) will perform the exam following the protocol of the Shriners Hospital for Children's motion lab.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Adolescents with idiopathic scoliosis | Adolescents with idiopathic scoliosis |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| posterior spine fusion | Procedure | vertebrae are fused to straighten a spinal curve |
|
| Measure | Description | Time Frame |
|---|---|---|
| Motion Analysis | Gait and standing spine range of motion are measured using a 3-D motion capture system. | Pre-Operation visit (within 1 week prior to surgical date) |
| Motion Analysis | Gait and standing spine range of motion are measured using a 3-D motion capture system. | 1 Year Post-Operative |
| Motion Analysis | Gait and standing spine range of motion are measured using a 3-D motion capture system. | 2 Years Post-Operative |
| Measure | Description | Time Frame |
|---|---|---|
| Functional Questionnaires | A functional outcome questionnaire filled out by the parents and patient. | Collected at Pre-Operative visit (1 week prior to surgical date) |
| Functional Questionnaires |
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Inclusion Criteria:
Exclusion Criteria:
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Adolescents with idiopathic scoliosis that have a Cobb angle greater than 50 degrees.
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| Name | Affiliation | Role |
|---|---|---|
| Sahar Hassani, MS | Shriners Hosptials for Children | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Shriners Hospitals for Children | Chicago | Illinois | 60707 | United States |
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| ID | Term |
|---|---|
| D012600 | Scoliosis |
| ID | Term |
|---|---|
| D013121 | Spinal Curvatures |
| D013122 | Spinal Diseases |
| D001847 | Bone Diseases |
| D009140 | Musculoskeletal Diseases |
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A functional outcome questionnaire filled out by the parents and patient.
| Collected at 1 year post-operative visit |
| e-med plantar pressures | A pressure map of the plantar surface of the foot during walking. | Collected at Pre-Operative visit (1 week prior to surgical visit) |
| Postural Stability | Standing balance and postural stability are measured using a NeuroCom Equitest System and Twin Forceplate system. | Pre-Operative (1 week prior to surgical visit) |
| Functional Questionnaires | A functional outcome questionnaire filled out by the parents and patient. | Collected at 2 year follow up |
| e-med plantar pressures | A pressure map of the plantar surface of the foot during walking. | Collected at 1 year follow up |
| e-med plantar pressure | A pressure map of the plantar surface of the foot during walking. | 2 year follow up |
| Postural Stability | Standing balance and postural stability are measured using a NeuroCom Equitest System and Twin Forceplate system. | 1 Year post-operative visit |
| Postural Stability | Standing balance and postural stability are measured using a NeuroCom Equitest System and Twin Forceplate system. | 2 year post-operative follow up |