Nerve Transfer Surgery to Restore Upper-limb Function After Cervical Spinal Cord Injury
Study Details
Study Description
Brief Summary
The goal of this prospective, open label cohort study is to assess functional and motor outcomes in individuals with cervical spinal cord injury who have undergone nerve transfer surgery, with the goal of increasing upper limb function. We will also compare these outcomes to a cohort of similarly matched individuals who have not undergone nerve transfer surgery, using robust outcome measures, rigorous pre-operative clinical and neurophysiological assessments, and standardized rehabilitation. At the end of this project we aim to develop a model for predicting nerve transfer outcomes using pre-operative clinical and neurophysiological characteristics.
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Detailed Description
The purposes of this study are:
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To quantify functional and motor outcomes of NT in patients with SCI, using robust outcome measures, rigorous pre-operative clinical and neurophysiological assessments, and standardized rehabilitation, and to compare these outcomes against individuals who did not undergo nerve transfer surgery.
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To develop a model for predicting NT outcomes using pre-operative clinical and neurophysiological characteristics.
Outcome measures:
Purpose 1: The primary study outcome is the Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP Ver. 1). Secondary outcomes are the Spinal Cord Independence Measure (SCIM) and motor outcomes in recipient muscles following NT, including muscle strength and neurophysiological assessments at 3 months intervals post-operatively, to final outcome measurement at 24 months.
Purpose 2: Relevant demographic, clinical variables and neurophysiological variables (including joint range of motion, muscle spasticity, pain, depression motor unit number estimation in recipient muscles and ultrasound evaluation of recipient muscle quality), are a priori variables that will be collected at baseline, in order to develop a clinical prediction tool to inform prognosis.
Research Design:
All SCI individuals referred to an interdisciplinary clinic for potential nerve transfer will undergo a standardized clinical examination, according to the International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI), to classify neurological level of injury. As well, electrodiagnostic test which will be performed by one of our highly qualified physicians. Individuals who are deemed candidates for nerve transfer surgery will be screened and invited to participate in the study. Participation in the study will not, in any way, influence clinical care.
After receiving written consent, outcome measurement will take place pre-operatively, then at 3-month intervals post operatively; final analysis will occur at 24 months after surgery. As well, a control group consisting of those SCI individuals who chose to not undergo or are not candidates for surgery will be recruited. This "control group" will undergo assessments at 24 months following their injuries, in line with the anticipated functional plateau in spontaneous recovery expected . Outcome measurement will be performed at GF Strong Rehabilitation Hospital (Primary site), the International Collaboration on Repair Discoveries (ICORD), Sunnybrook Hospital in Toronto, and Kingston Health Science Centre. Rehabilitation will be administered by highly qualified hand therapists with standardized frequency, and duration for all individuals. All study data will be stored in a REDCap database which will be shared between all participating institutions.
Outcome measurement & information collected include:
Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP), which is a validated upper limb functional measure, specifically designed for use in SCI (Kalsi-Ryan et al. 2012). It incorporates three domains vital to upper limb function: sensation, strength, and prehension. It is a multimodal test comprising 5 subtests for each upper limb: dorsal sensation, palmar sensation, strength, prehension ability and prehension performance. The GRASSP results in 5 numerical scores that provide a comprehensive profile of upper-limb function and will be administered by GRASSP certified research personnel. As well, individuals will be asked to complete the Spinal Cord Independence Measure (SCIM) questionnaire (Catz A, et al. 1997) on the same day of their visit.
At Baseline, a validated technique called motor unit number estimation (MUNE) counts the number of MN's and can be essential in evaluating MN health. We aim to carry out this technique towards measuring the health of MN's in functionally relevant muscles in patients with SCI and comparing this with healthy controls. The purpose of this study is to provide a quantitative measure of the size of MN pool in clinically relevant muscles below the level of SCI using MPS and MScan MUNE. We will also supplement information about MNs with ultrasound-derived measures of muscle quality.
Ultrasound sonography recording will be taken to analyze the structural health of recipient muscles and to quantify muscle fibrosis and atrophy. The muscles of interest will be anatomically identified and marked, and ultrasound gel will be applied to skin surface of the upper limb prior to placing the ultrasound probe. Individuals will be asked to lie in a dimly lit room for this portion of the study.
Demographic information will be collected for each participant, including
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age;
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sex;
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medical comorbidities; and
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medications
Clinical factors influencing functional and motor recovery in SCI will be measured:
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spasticity with modified Ashworth scores;
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depression with Beck's depression inventory (Beck, A. T., et al. 1996);
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passive ranges of motion in joints targeted by NT; and
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brief pain inventory (Ullrich PM, et al. 2008).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
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| Experiemental: Surgical Arm Individuals in this group will receive nerve transfer surgery 6 - 9 months post cervical spine injury and be observed for two years post-operatively. |
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| Control: Non-surgical Individuals in this group will not have undergone nerve transfer surgery. They will be observed for two years post injury while receiving standard of care including medical and rehabilitation. We want to reinforce that individuals are not being randomized to surgery versus non-surgery. Rather individuals this group will either have made the decision not to undergo surgery, independent their participation in this study. |
Outcome Measures
Primary Outcome Measures
- Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP) [Baseline then every 3 months for 2 years]
A validated upper limb functional measures and previously is used in SCI (Kalsi-Ryan et al. 2012) incorporates three domains vital to upper limb function: sensation, strength, and prehension.
Secondary Outcome Measures
- Modified Ashworth scores (MAS) [Baseline then every 3 months for 2 years]
Modified Ashworth Scale (MAS) have been utilized in spinal cord injury patient population to assess spasticity by examining muscle tones.
- Range of Motion [Baseline then every 3 months for 2 years]
A Goniometer is used to measure range of motion of the joint angles (degrees) from the axis of the joint. The measurement of joint movements is compared to its full potential.
- Ultrasound [Baseline then every 3 months for 2 years]
Ultrasound imaging to assess the structural health of recipient muscles and to quantify muscle fibrosis and atrophy.
- Spinal Cord Independence Measure (SCIM) [Baseline then every 3 months for 2 years]
The SCIM has been developed to address three specific areas of function in patients with spinal cord injuries such as activities of daily living, respiration and sphincter management, and a patient's mobility abilities.
- Douleur Neuropathique 4 (DN-4) [Baseline then every 3 months for 2 years]
A questionnaire consisting of 10 items and can be useful in assessment of neuropathic pain. The items related to pain quality are based on an interview and examination of the patient.
- Beck's Depression Inventory (BDI) [Baseline then every 3 months for 2 years]
The questionnaire is a 21-item, self-report rating inventory that measures characteristic attitudes and symptoms of depression.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Motor complete (AIS A or B) between neurological level of injury C5 and C8
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Able to provide informed written consent
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Able to attend and comply with the testing protocols
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Able to understand and speak English or have access to an appropriate interpreter as judged by the investigator.
Exclusion Criteria:
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An uncontrolled medical condition (e.g. uncontrolled cardiovascular disease, diabetes, kidney or liver disease)
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Have ever received botulinum toxin injections (Botox) for tone management in the upper limb
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An unmanaged secondary complication of SCI including but not limited to uncontrolled neuropathic pain or spasticity, syringomyelia, fracture, urinary tract infection or significant pressure ulcer, preventing participation in testing
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
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| 1 | GF Strong Rehabilitation Hospital | Vancouver | British Columbia | Canada | V5Z 2G9 |
| 2 | QEII Health Sciences Centre | Halifax | Nova Scotia | Canada | B3H 3A7 |
| 3 | Kingston Health Sciences Centre | Kingston | Ontario | Canada | K7L 5G2 |
| 4 | Sunnybrook Health Sciences Centre | Toronto | Ontario | Canada | M4N 3M5 |
Sponsors and Collaborators
- University of British Columbia
- Queen's University
- Dalhousie University
- University of Toronto
- Wings for Life
Investigators
- Principal Investigator: Michael Berger, MD, PHD, University of British Columbia
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- H20-03350