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Clinical Trials/NCT03989752
NCT03989752
Terminated
Not Applicable

Effects of an Overground Walking Program With Robotic Exoskeleton in Long-term Manual Wheelchair Users With a Chronic Spinal Cord Injury

Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal1 site in 1 country16 target enrollmentMarch 14, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Cord Injuries
Sponsor
Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal
Enrollment
16
Locations
1
Primary Endpoint
Change in muscle size
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

Many individuals with a spinal cord injury (SCI) use a wheelchair as their primary mode of locomotion. The prolonged non-active sitting time associated to this mode of locomotion contributes to development or worsening of numerous adverse health effects affecting musculoskeletal, endocrino-metabolic and cardiorespiratory health. To counter this vicious circle, engaging in a walking program with a wearable robotic exoskeleton (WRE) is a promising physical activity intervention. This study aims to measure the effects of a WRE-assisted walking program on musculoskeletal, endocrino-metabolic and cardiorespiratory health.

Detailed Description

Many individuals with a spinal cord injury (SCI) rely on manually propelled wheelchairs as their primary source of locomotion, leading to increased non-active sitting time, reduced physical activity and reduced lower extremity (L/E) weight bearing. This contributes to the development or worsening of complex and chronic secondary health problems, such as those affecting musculoskeletal (e.g., osteoporosis), endocrine-metabolic (e.g., hypertension, dyslipidemia, type 2 diabetes) and cardiorespiratory (e.g., poor aerobic fitness) health. Ultimately, these health problems may negatively affect functional capabilities and reduce quality of life. Preliminary evidence has shown that engaging in a walking program with a wearable robotic exoskeleton (WRE) is a promising intervention. In fact, WRE-assisted walking programs promote L/E mobility and weight bearing (a crucial stimulus for maintaining bone strength in individuals with SCI), while also soliciting the trunk and upper extremity muscles and cardiorespiratory system. This study aims to measure the effects of a WRE-assisted walking program on 1) bone strength, bone architecture and body composition, 2) endocrino-metabolic health profile and 3) aerobic capacity. Twenty (20) individuals with a chronic (\> 18 months) SCI will complete 34 WRE-assisted training sessions (1 h/session) over a 16-week period (1-3 sessions/week). Training intensity will be progressed (i.e., total standing time, total number of steps taken) periodically to maintain a moderate-to-vigorous intensity (≥ 12/20 on the Borg Scale). All training sessions will be supervised by a certified physical therapist. Main outcomes will be measured one month prior to initiating the WRE-assisted walking program (T0), just before initiating the WRE-assisted walking program (T1), at the end of the WRE-assisted walking program (T2) and two months after the end of the WRE-assisted walking program (T3). Descriptive statistics will be used to report continuous and categorical variables. The alternative hypothesis, stipulating that a pre-versus-post difference exists, will be verified using Repeated Mesures ANOVAs or Freidman Tests.

Registry
clinicaltrials.gov
Start Date
March 14, 2019
End Date
January 7, 2022
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal
Responsible Party
Principal Investigator
Principal Investigator

Dany H. Gagnon

Senior researcher

Centre for Interdisciplinary Research in Rehabilitation of Greater Montreal

Eligibility Criteria

Inclusion Criteria

  • Traumatic or non-traumatic spinal cord injury between C6 and T10 neurological level at least 18 months pre-enrollment
  • Long-term wheelchair use as primary means of mobility (non-ambulatory)
  • Normal cognition (Montreal Cognitive Assessment Score ≥26/30)
  • Understand and communicate in English of French
  • Reside in the community within 75 km of the research site
  • Exoskeleton-specific inclusion criteria:
  • Body mass ≤100 kg
  • Height=1.52-1.93 m
  • Pelvis width=30-46 cm
  • Thigh length=51-61.4 cm

Exclusion Criteria

  • Other neurological impairments aside from those linked to the spinal cord injury (e.g., severe traumatic brain injury)
  • Concomitant or secondary musculoskeletal impairments (e.g., hip heterotopic ossification)
  • History of lower extremity fracture within the past year
  • Unstable cardiovascular or autonomic system
  • Pregnancy
  • Any other other conditions that may preclude lower extremity weight-bearing, walking, or exercise tolerance in the wearable robotic exoskeleton
  • Exoskeleton-specific exclusion criteria:
  • Inability to sit with hips and knees ≥90° flexion
  • Lower extremity passive range of motion limitations (hip flexion contracture ≥5°, knee flexion contracture ≥10°, and dorsiflexion ≤-5° with knee extended)
  • Moderate-to-sever lower extremity spasticity (\>3 modified Ashworth score)

Outcomes

Primary Outcomes

Change in muscle size

Time Frame: One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2), two months after the end of the walking program (T3)

Cross-sectional images of the radius, tibia and femur captured with pQCT will be used to measure muscle cross-sectional area.

Change in bone mass density (BMD) and architecture in the lower extremity

Time Frame: One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2), two months after the end of the walking program (T3)

Areal BMD will be calculated with dual-energy X-ray absorptiometry (DXA) at the proximal tibial plateau, distal femur, femoral neck and the 1st to the 4th lumbar vertebrae. Volumetric BMD and microarchitecture parameters of the trabecular and cortical bones (mineral content, mineral density, cross-sectional area, cortical thickness) at the distal femur and proximal tibia will be captured with peripheral quantitative computed tomography (pQCT).

Change in intramuscular fat infiltration

Time Frame: One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2), two months after the end of the walking program (T3)

Cross-sectional images of the radius, tibia and femur captured with pQCT will be used to measure intramuscular fat infiltration (i.e., muscle density).

Change in body composition

Time Frame: One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2), two months after the end of the walking program (T3)

DXA scans will be used to quantify total and regional body fat and fat free tissue mass (and relative percentages).

Secondary Outcomes

  • Change in lipide profile(One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2))
  • Change in inflammatory biomarkers(One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2))
  • Change in bone turnover biomarkers(One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2))
  • Change in glycemic biomarkers(One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2))
  • Change in insulin resistance(One month prior to intiating the walking program (T0), baseline at the initiation of the walking program (T1), at the end of the walking program (T2))
  • Change in aerobic capacity(Baseline at the initiation of the walking program (T1), at the end of the walking program (T2))

Study Sites (1)

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