The Effects of Incorporated Exoskeletal-Assisted Walking in Spinal Cord Injury (SCI) Acute Inpatient Rehabilitation
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Change in Spinal Cord Independence Measure (SCIM) Version III Scores
研究概览
简要总结
The purpose of this research study is to test the effect of early exoskeletal-assisted walking (EAW) training (combined into regular acute inpatient rehabilitation (AIR)) on improving functional recovery and reducing pain and inflammation. Powered exoskeletons are a technology that offer standing and walking for certain persons with spinal cord injury (SCI) who meet the using indication of the device and have been used in the chronic SCI population with positive benefits in ability to move, daily function (such as bathing and dressing), body composition (such as lean and fat tissue mass), and quality of life (QOL). Despite the potential for EAW to promote functional recovery and reduce secondary medical complications (such as urinary tract infections and pain), no reports exist on the use of exoskeletons in AIR.
详细描述
People with spinal cord injury (SCI) can have an abrupt loss of upright mobility, function and physical activity. Inflammation and pain are reported to be increased, with negative impacts on quality of life. Powered exoskeletons are a technology that offer standing and walking for eligible persons with SCI and have predominantly been used in the chronic SCI population with positive benefits in mobility, function, body composition, and quality of life (QOL). Despite the potential for exoskeletal-assisted walking (EAW) to promote functional recovery and mitigate secondary medical complications, no reports exist on the use of exoskeletons in acute inpatient rehabilitation (AIR). The goal of this study is to test the effect of early EAW training (incorporated into regular AIR) on accelerating functional recovery and reducing pain and inflammation. A total of 30 people with non-progressive SCI (≥18 years; <6 months after SCI), who are clinically eligible for gait training during AIR, will be randomly assigned into one of two groups (15 participants/group, stratified evenly for traumatic and non-traumatic SCI). The intervention group will receive gait training with an Ekso powered exoskeleton, incorporated into usual 3-hour AIR (AIR with EAW group). The control group will have usual 3-hour AIR, but without using an exoskeleton (AIR only group). Motor function, functional activities, pain and inflammation will be assessed after enrollment in the study and before discharge from AIR. The intervention group is expected to have significantly better outcomes compared with the control group. The impact of successful completion of this study would increase knowledge of the effect of using EAW during acute/subacute AIR. The expected outcome of this study is that exoskeletal-assisted walking during AIR will have significantly greater effects on mitigating some of the secondary consequences of paralysis from SCI during the early phases of recovery and rehabilitation.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
盲法说明
The outcome assessors are not part of intervention. They will not know which group participants will be in.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age 18 years or greater
- •Height between 5'2" and 6'2" (1.6 meters to 1.9 meters)
- •Weight less than 220 pounds (100 kilograms)
- •Hip: 5 degrees of extension; 110 of flexion
- •Knee: Full extension to 110 of flexion
- •Ankle: at least 0 of dorsiflexion to 25 of plantarflexion
- •Are eligible for locomotor training as part of inpatient rehabilitation
- •Independent with static sitting balance
- •Sufficient function upper extremity strength to manage walking aid (front-wheeled walker, platform walker, or crutches)
- •Able to follow directions
排除标准
- •Uncontrolled cardiovascular conditions (i.e. heart failure, angina, hypertension)
- •Inability to stand upright due to orthostatic hypotension
- •Any form of progressive SCI as defined by the physician, such as cancers
- •Body characteristics that do not fit within exoskeleton limits
- •Upper leg length discrepancy > 0.5" or lower leg discrepancy >0.75"
- •Skin integrity issues in areas that would contact the device or that would likely be made worse by device use
- •Pregnancy
- •Colostomy
- •Mechanical ventilation
- •Non-English Speaking
- •The participant is able to walk better with exoskeleton assistance at baseline
- •Any other issue that might prevent safe standing or walking
研究组 & 干预措施
Exoskeletal-assisted walking training group
Participants will receive locomotor training provided with an Ekso™ powered exoskeleton according to the standard of care of AIR at Mount Sinai Hospital with the exception that the EAW training will be incorporated into the designated therapy times (3 hours of physical therapy (PT) and/or occupational therapy (OT)) which will be provided as determined by the clinical team from the earliest time they are identified to be able to safely stand, through discharge. The goal of EAW intervention is to complete three or more sessions of EAW training a week during the AIR period (after enrolling into the study until discharge).
干预措施: Ekso™ powered exoskeleton (Device)
Exoskeletal-assisted walking training group
Participants will receive locomotor training provided with an Ekso™ powered exoskeleton according to the standard of care of AIR at Mount Sinai Hospital with the exception that the EAW training will be incorporated into the designated therapy times (3 hours of physical therapy (PT) and/or occupational therapy (OT)) which will be provided as determined by the clinical team from the earliest time they are identified to be able to safely stand, through discharge. The goal of EAW intervention is to complete three or more sessions of EAW training a week during the AIR period (after enrolling into the study until discharge).
干预措施: Standard of care (Other)
Standard of care group
Participants will receive standard of care of acute inpatient rehabilitation which includes three hours of physical therapy and/or occupational therapy per day until they are discharged.
干预措施: Standard of care (Other)
结局指标
主要结局
Change in Spinal Cord Independence Measure (SCIM) Version III Scores
时间窗: Baseline and before discharge from acute inpatient rehabilitation (average 2-3 weeks)
Functional activities will be assessed using Spinal Cord Independence Measure (SCIM) scores evaluated by clinicians. Full Scale range from 0-100, higher score indicates more independence. Each subscale score is evaluated within the 100-point scale (self-care: 0-20; respiration and sphincter (R \& S) management: 0-40; mobility: 0-40)
次要结局
- Change in International Standards for Neurological Classification of SCI (ISNCSCI)(Baseline and before discharge from acute inpatient rehabilitation (average 2-3 weeks))
- Change in International Spinal Cord Injury Basic Pain Data Set (ISCIBPDS) 2.0(Baseline and at discharge from acute inpatient rehabilitation (average 2-3 weeks))
- Number of Participants With Neuropathic Pain(Baseline and discharge from acute inpatient rehabilitation (average 2-3 weeks))
研究者
Ann M. Spungen EdD
Vice Chairperson of Research, Department of Rehabilitation and Human Performance
Icahn School of Medicine at Mount Sinai