The goal of this clinical trial is to examine the long-term use of a personal overground robotic exoskeleton in subjects with spinal cord injury. The main aims of this study include:
1. Determine patterns of personal overground robotic exoskeleton use over 12 months.
2. Examine the impact of personal overground robotic exoskeleton use on health outcomes over 12 months. These will include:
1. Objective health - heart rate, physical activity, sleep behavior, body temperature, body-mass index, and bone density
2. Medical status - rehospitalization, infection frequency, pressure injury, falls, fractures, medication (type/dose)
3. Function - bowel function, bladder function, pain, spasticity, quality of life, mental health, social participation
3. Determine healthcare expenditure over 12 months
Participants and their support person(s) will be trained on using a personal robotic exoskeleton in their home and community. Once they complete training, they will use the exoskeleton as they wish (ie, no requirement to use the device a certain number of times per week) and data collection will begin.
Protocol Amendment History
1 amendment
This ClinicalTrials.gov record has been amended once since 2025-06-12.