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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

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device, Other
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Spain
Hospital Universitario de Vall d'Hebron
RECRUITING
Barcelona
Hospital Nacional de Parapléjicos
NOT_YET_RECRUITING
Toledo
Contact Information
Primary
Lluïsa Montesinos Magraner, Dr
lluisa.montesinos@vallhebron.cat
+34 620951308
Time Frame
Start Date: 2026-01-15
Estimated Completion Date: 2027-09-30
Participants
Target number of participants: 80
Treatments
Experimental: Robotic exoskeleton
The intervention group will receive rehabilitation treatment with the ABLE Exoskeleton
Active_comparator: Conventional therapy
The control group will receive conventional therapy for gait rehabilitation
Related Therapeutic Areas
Sponsors
Leads: ABLE Human Motion S.L.
Collaborators: Hospital Universitari Vall d'Hebron Research Institute, Universitat de Lleida, Hospital Nacional de Parapléjicos de Toledo

This content was sourced from clinicaltrials.gov