RecruitingNot ApplicableNCT07036107

A Trial on the Clinical and Socioeconomic Impact of Wearable Exoskeletons for Spinal Cord Injury Rehabilitation in the Spanish Healthcare System

Robotic-SNS: A Multicenter, Randomized Trial on the Clinical and Socioeconomic Impact of Wearable Exoskeletons for Spinal Cord Injury Rehabilitation in the Spanish Healthcare System

Sponsor

ABLE Human Motion S.L.

Enrollment

80 participants

Start Date

Jan 15, 2026

Study Type

INTERVENTIONAL

Conditions

Spinal Cord Injury

Summary

This clinical trial aims to collect evidence on the clinical benefits and the socioeconomic impact of integrating a novel wearable powered lower-limb exoskeleton for gait rehabilitation in acute/subacute spinal cord injured individuals and to evaluate the efficiency of this technology to the current standard of care in the Spanish Healthcare System (SNS).. The main questions it aims to answer are: * Is robotic therapy for gait rehabilitation more effective and efficient than conventional therapy? * Does robotic therapy for gait rehabilitation reduce the burden on healthcare professionals and caregivers? * Does robotic therapy for gait rehabilitation reduce direct healthcare costs? * Does robotic therapy for gait rehabilitation reduce intervention-related costs? Researchers will compare a novel wearable powered lower-limb exoskeleton for gait rehabilitation to conventional therapy to see if the robotic exoskeleton is more effective and efficient in improving clinical benefits and to assess if it reduces the burden of healthcare professionals and caregivers, as well as healthcare and intervention-related costs. Participants will: * Be randomized on a 1:1 basis to receive rehabilitation treatment with either the robotic exoskeleton or conventional therapy for gait recovery, 3 times a week on non-consecutive days for 8 weeks (24-session program). * Undergo a pre- and post-intervention assessment of clinical, functional, physiological, psychological, and socioeconomic variables. * Have a follow-up visit 2 months after the end of the treatment.

Eligibility

Min Age: 18 YearsMax Age: 70 Years

Inclusion Criteria8

diagnosis of spinal cord injury (SCI) in the acute or subacute phase (< 6 months of evolution)
traumatic or non-traumatic aetiology
neurological level of the SCI between C5 and L5 for patients with American Spinal Injury Association Impairment Scale (AIS) C or D, and SCI between C7 and L5 for patients with AIS A or B.
sufficient strength in the upper extremities to handle a walker (triceps muscle score ≥ 4 according to the Medical Research Council (MRC) scale).
range of motion (ROM) without limitations in the lower extremities (achieve at least a knee extension of 10 degrees and neutral ankle position)
muscle spasticity in the lower extremities with a score ≤ 3 on the Modified Ashworth Scale (MAS)
tolerate bipedalism (having stood up in the last year)
aged between 18 and 70 years, with height between 150 cm and 190 cm, and weight less than 100 kg

Exclusion Criteria12

WISCI ≥ 15
cognitive or neurological limitations that prevent following instructions
another neurologic disorder permanently affecting gait and gait therapy (other than SCI)
grade I or higher in the European Pressure Ulcer Advisory Panel (EPUAP) in the areas of contact with the exoskeleton
unresolved fractures at the time of the study
uncontrolled autonomic dysautonomia
intolerance to exercise
uncontrolled epilepsy
previous experience with Robotic-Assisted Gait Training (RAGT).
ROM restriction such as flexing or arthrodesis will be excluded
spinal instability (or spinal orthotics unless cleared by a medical doctor).
deterioration >3 points of the total in the motor score of the International Standards for the Neurological Classification of Spinal Cord Injury (ISNCSCI) in the last 4 weeks. Loss of sensation and/or motor activity above the level of injury detected that has not been evaluated by a doctor.

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Interventions

DEVICEABLE Exoskeleton

Participants will receive a 24-session rehabilitation treatment program with the ABLE Exoskeleton, 3 times a week for up to 8 weeks

OTHERConventional therapy

Participants will receive a 24-session conventional therapy program for gait rehabilitation, 3 times a week for up to 8 weeks. Conventional therapy includes joint mobilizations, strengthening of paretic muscles and re-education of walking with parallel bars, making use of the technical aids and orthoses required by the patient (KAFOs, crutches and walkers).