Spinal Curvatures Clinical Trial
Official title:
The Effect of Thoracolumbar Spinal Deformity and Its Surgical Correction on Gait and Balance in Adults
Surgical intervention may provide pain relief and improvement in function but one area of significant clinical interest is the restoration/improvement in gait and functional balance. Based on the investigators knowledge, there is limited literature on biomechanics and neuromuscular control of the lower extremities and spine as assessed by objective gait analysis and balance strategies in adult degenerative scoliosis patients, pre and post surgical intervention. The purpose of this study is to determine the impact of spinal deformity on the biomechanics and neuromuscular control of the lower and upper extremities, and also investigate the impact of surgery on these functions as evaluated by gait and balance analyses using dynamic EMG, video motion capture and force plate analysis and also to compare these patients with healthy controls to better evaluate the extent of limitations before and after surgery.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | December 2018 |
Est. primary completion date | December 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 30 Years and older |
Eligibility |
Inclusion Criteria: 1. Age 30 years and older 2. Clinically diagnosed thoracolumbar and/or lumbo-sacro-pelvic deformity as defined by the SRS/Schwab classification systems as Cobb angle of 25° or greater 3. Instrumentation to be used at 4 or more levels 4. Able to ambulate without assistance and stand without assistance with participant eyes open for a minimum of 10 seconds 5. Able and willing to attend and perform the activities described in the informed consent within the boundaries of the timelines set forth for pre-, and post-operative follow-up Exclusion Criteria: 1. History of prior attempt at fusion (successful or not) at the indicated levels, (history of one level fusion is not an exclusion) 2. Major lower extremity surgery or previous injury that may affect gait (a successful total joint replacement is not an exclusion) 3. BMI higher than 35 4. Neurological disorder, diabetic neuropathy or other disease that impairs the patient's ability to ambulate or stand without assistance 5. Usage of blood thinners 6. Major trauma to the pelvis 7. Pregnant or wishing to become pregnant during the study |
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Basic Science
Country | Name | City | State |
---|---|---|---|
United States | Texas Back Institute | Plano | Texas |
Lead Sponsor | Collaborator |
---|---|
Texas Back Institute | Alphatec Spine, Inc. |
United States,
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* Note: There are 26 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Kinematic Variables Change assessed with human motion capture system | 3-Dimensional Range of Motion (ROM) during the stance and swing phase. | Prior to surgery; 3 and 12 months after surgery | No |
Primary | Kinetic Variables Change assessed with human motion capture system | Vertical Ground Reaction Forces (GRF) | Prior to surgery; 3 and 12 months after surgery | No |
Primary | Electromyography Variables Change assessed with an Electromyograph | Bilateral peak magnitude during the stance phase | Prior to surgery; 3 and 12 months after surgery | No |
Primary | Spatio-Temporal Variables Change assessed with human motion capture system | Walking Speed | Prior to surgery; 3 and 12 months after surgery | No |
Secondary | Patient Self-Reported Outcome Assessments Change | Visual Analog Scale (VAS) | Prior to surgery; 3 and 12 months after surgery | No |
Secondary | Patient Self-Reported Outcome Assessments Change | Scoliosis Research Society (SRS) -22 | Prior to surgery; 3 and 12 months after surgery | No |
Secondary | Patient Self-Reported Outcome Assessments Change | Neck Disability Index (NDI) | Prior to surgery; 3 and 12 months after surgery | No |
Secondary | Patient Self-Reported Outcome Assessments Change | Oswestry Disability Index (ODI) | Prior to surgery; 3 and 12 months after surgery | No |
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