Clinical Evaluation and Rehabilitation System for Dynamic Balance Control in Cervical Myelopathy Patients

Cervical Myelopathy Clinical Trial

Official title:

Clinical Evaluation and Rehabilitation System for Dynamic Balance Control in Cervical Myelopathy Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02842775
• Other study ID #: 201512167RINB
• Status: Completed
• Phase: N/A
• Start date: January 2016
• Est. completion date: January 22, 2018

Study information

• Verified date: April 2019
• Source: National Taiwan University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cervical myelopathy is common among the aging population.One of the complications of cervical myelopathy is balance impairment.In this study, the patients with cervical myelopathy undergo biomechanical, imaging, neurophysiological and functional assessment. Besides, the dynamic balance training is introduced to the patients with cervical decompression surgery.This study is expected to provide important empirical evidence to evaluate the prognosis of the surgery, to further guide the postoperative rehabilitation of myelopathy patients and to improve patients' long-term quality of life.

Description:

Taiwan is quickly becoming a nation of the aging population with myelopathy reporting to be one of the most common spinal cord disorders associated with spinal degeneration. Given the high prevalence rate of the condition, current project aims to investigate the impact of myelopathy on motor control from a biomechanical perspective with the overall aim to develop an interactive balance perturbation rehabilitation program targeting individual patients and identified the deficiency. The efficacy of the individual rehabilitation program will be assessed and determined to utilize a prospective longitudinal study design. A break down of the proposed three-year project are as follows:

Year 1: Myelopathy patients prepared to receive cervical decompression surgery as well as age-matched asymptomatic controls will be recruited and subjected to the following clinical evaluations: 3-dimensional biomechanical motion analysis, diagnostic Magnetic Resonance Imaging, pain and disability questionnaires, motor performance assessment, spinal curvature, muscle strength assessment as well as transcranial magnetic stimulation examination. Motor control and coordination of functional movements will also be evaluated.

Year 2: Continue to recruit potential participants and further develop the use of the interactive split-belt balance perturbation treadmill as modalities for gait and balance therapy.

Year 3: Physical Therapy rehabilitation programs at 3-month post surgery, one group will participate in a specific and personalized interactive balance perturbation training program targeting balance and gait retraining, while the other group receives the routine Physical Therapy program. Both treatment groups will be assessed pre-operatively, at 3, 6 and 12 months postoperatively. Patients will be classified based on their severity and grade of the spinal cord compression before being compared for any difference in treatment responses.

Year 4: Follow-up monitoring and documenting the number of falls experienced by patients at one year postoperatively as an outcome of effectiveness.

Expected outcome and significance The findings from the current project will provide important empirical evidence to guide the postoperative rehabilitation of myelopathy patients. Through detailed biomechanical motion analysis, it is anticipated that this project will provide an in-depth understanding of the influence of decompression surgery on motor control and spinal stability. The tailored and innovative rehabilitation program will also improve patients' long-term quality of life.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: January 22, 2018
• Est. primary completion date: January 22, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 40 Years to 80 Years

Eligibility

Inclusion criteria:

• Aged 40-80 years old

• Diagnosed cervical myelopathy according MRI imaging

• Able to stand more than 30 seconds

Exclusion criteria:

• With rheumatoid arthritis, ankylosing spondylitis,multiple sclerosis and other systemic disorders

• With musculoskeletal or neurological disorders,which can impair balance

• With previous spinal surgery

• Unable to communicate or follow instruction

• Not suit to cervical decompressive surgery or physical therapy due to other medical condition

Related Conditions & MeSH terms

• Bone Marrow Diseases
• Cervical Myelopathy
• Spinal Cord Diseases

Intervention

Other:
• balance perturbation training
perturbation training on the split-belt balance perturbance treadmill,

Locations

Country	Name	City	State
Taiwan	National Taiwan University Hospital	Taipei

Sponsors (1)

Lead Sponsor	Collaborator
National Taiwan University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Kinematics (joint range of motion)	joint range of motion	1 year
Primary	Electromyography(EMG)	EMG of lower extremity	1 years
Primary	Muscle Strength Assessment by Dynamometer	Muscle strength of upper and lower extremity	1 years
Primary	Kinetic(Ground reaction force)	Ground reaction force	1 years
Primary	Transcranial magnetic stimulation (TMS)		1 years
Secondary	Visual Analog Scale (VAS)		3 years
Secondary	Neck Disability Index (NDI)		3 years
Secondary	Japanese Orthopaedic Association Myelopathy Evaluation Questionnaire(JOACMEQ)		3 years
Secondary	Nurick Classification		3 years
Secondary	Five Times Sit to Stand Test		3 years
Secondary	Timed Up & Go test (TUG)		3 years
Secondary	Dynamic Gait Index (DGI)		3 years