~6 spots leftby Apr 2026

Exoskeletal-assisted Walking to Improve Mobility, Bowel Function and Cardio-Metabolic Profiles in Persons With SCI

(EAWSCI Trial)

Recruiting in Palo Alto (17 mi)
+2 other locations
AM
Overseen byAnn M Spungen, EdD
Age: 18+
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Academic
Waitlist Available
Sponsor: James J. Peters Veterans Affairs Medical Center
No Placebo Group

Trial Summary

What is the purpose of this trial?

The primary objective of this study is to achieve successful walking skills using exoskeletal walking devices over the course of 36 sessions in 3 months at specific velocities and distances in people with chronic SCI who are wheelchair dependent for community mobility. The secondary objectives are to determine if this amount of exoskeletal walking is effective in improving bowel function and body composition in the same patient population. The exploratory objectives are to address additional questions concerning the retention or non-retention of the positive changes, the effects of the increased physical activity from this intervention on vagal tone, orthostatic tolerance, lipid profile, total testosterone, estradiol levels, and quality of life (QOL). A Phase III randomized clinical trial (RCT) will be performed using a crossover design and employing an exoskeletal-assisted walking intervention. The experimental arm will be compared to a usual activities (UA) arm, as the control, in 64 persons with chronic SCI (\>6 month post injury) who are wheelchair-dependent for outdoor mobility in the community. The WALK arm will consist of supervised exoskeletal-assisted walking training, three sessions per week (4-6 h/week) for 36 sessions for their second 12-week period. The UA arm will consist of identification of usual activities for each participant, encouragement to continue with these activities and attention by study team members throughout the 12-week UA arm. These activities will be recorded in a weekly log. The investigators hypotheses are that 1) this exoskeletal intervention will be successful in training ambulatory skills in this patient population, 2) the exoskeletal intervention will be better than a control group in improving body composition, bowel function, metabolic parameters and quality of life in the same population.

Research Team

AM

Ann M Spungen, EdD

Principal Investigator

James J Peters VAMC

Eligibility Criteria

Inclusion Criteria

Males and females, between 18-70 years old
Traumatic or non-traumatic paraplegia >6 months in duration
SCI motor deficit at any level
See 5 more

Treatment Details

Interventions

  • Exoskeletal-assisted walking (Other)
Participant Groups
2Treatment groups
Experimental Treatment
Active Control
Group I: Exoskeletal-Assisted Walking (WALK)Experimental Treatment1 Intervention
WALK first for 12 weeks (36 sessions)
Group II: Usual Activities (UA)Active Control1 Intervention
Usual activities first for 12 weeks

Find a Clinic Near You

Research Locations NearbySelect from list below to view details:
Univerity of Maryland rehabilitation and Orthopaedic Institute (UMROI)Baltimore, MD
Kessler Foundation Research Center (KFRC)West Orange, NJ
James J Peteres VA Medical CenterThe Bronx, NY
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Who Is Running the Clinical Trial?

James J. Peters Veterans Affairs Medical Center

Lead Sponsor

Trials
59
Patients Recruited
2,900+