Houston, Texas 77030


Purpose:

The purpose of this study is to investigate whether a wearable robotic exoskeleton can help people with multiple sclerosis (MS) to walk again.


Study summary:

Loss of the ability to walk is one of the significant problems in persons with multiple sclerosis (MS). This limitation prevents the person from having an active and meaningful life at home and in the community. Also, more energy is needed to walk, which can cause fatigue and further leads to a non-active life style and poor quality of life. Unfortunately, walking training is often not available for this population because of the severity and progress of the disease; therefore, a new strategy is needed to help people with MS to walk again. A new technology, the wearable robotic exoskeleton, has been developed to help persons with spinal cord injuries stand up and walk. The robotic legs are powered by batteries and controlled by motors. This study will investigate the use of a wearable robotic exoskeleton to help persons with MS to walk. Participants will receive trainings (5 days per week for 3 weeks) to walk with the robotic exoskeleton (EKSO, EKSO Bionics, Richmond, CA). During the training, a physical therapist will teach the participant how to maintain balance, sit to stand, stand to sit, and walk with the wearable robotic exoskeleton. The hypothesis is that persons with MS will be able to use a robotic exoskeleton to walk better and with less energy costs.


Criteria:

Subjects will be enrolled if they meet the following inclusion criteria: - Age 18 years or older - Ambulatory with assistive devices (Ambulation status will be determined by the EDSS score) - With an Expanded Disability Status Scale (EDSS) score between 6 and 7.5 inclusive - Height and weight are between 160 and 188 cm (5'2'' to 6'2''), and less than 100 kg (220 lb), respectively (per exoskeleton manufacturer) - Able to follow simple 3 step commends - Able to understand the study procedure and consent form Subjects will be excluded if they have any of the following exclusion criteria: - History of severe neurologic injuries other than MS (Spinal Cord Injury, Cerebral Palsy, Amyotrophic Lateral Sclerosis, Traumatic Brain Injury, Cerebral Vascular Accident, etc.) - Severe comorbidities: - active infections - heart, lung, or circulatory conditions - pressure ulcers - Documented severe osteoporosis affecting the hip and spine - Severe spasticity in the lower extremities (Modified Ashworth ≥ 3) or uncontrolled clonus - Unhealed limb or pelvic fractures - Skin issues that would prevent wearing the device - Range of motion restrictions that would prevent subject from achieving a normal, reciprocal gait pattern, or would restrict a subject from completing normal sit to stand or stand to sit transitions. - Upper extremity strength deficits that limit ability to balance with a front rolling walker or crutches. - Heterotopic ossification that resists functional range of motion in lower extremities - Contractures (>15 degrees at the hips or >20 degrees at the knees) - Psychiatric or cognitive comorbidities resulting in motor planning or impulsivity concerns - Colostomy - Have received any physical therapy intervention within 3 months prior to enrolment in the study - Non-English speaking


NCT ID:

NCT02519244


Primary Contact:

Principal Investigator
Shuo-Hsiu Chang, PT, PhD
The University of Texas Health Science Center, Houston

Shuo-Hsiu Chang, PT, PhD
Phone: 713-799-7016
Email: shuo-hsiu.chang@uth.tmc.edu


Backup Contact:

Email: ruta.pranjape@uth.tmc.edu
Ruta Paranjape, MS
Phone: 713-797-7132


Location Contact:

Houston, Texas 77030
United States

Shuo-Hsiu Chang, PT, PhD
Phone: 713-799-7016
Email: shuo-hsiu.chang@uth.tmc.edu

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 22, 2017

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