All trials - page: 11

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NCTID
Brief title
Sponsor
Design
Criteria
Status
Target enrollment
Study phase & design
Primary intervention type
Primary potential benefit
Outcome measure
Follow up
Start date
First posted
Location
NCT07407725Clinical Outcome Assessment for AT & BCIShirley Ryan AbilityLab
  • Age ≥ 18 yrs
  • Level C1-T1
  • AIS
  • All
Recruiting60NAGeneral health
  • American Spinal Injury Association Impairment Scale (AIS)
  • Canadian Occupational Performance Measure
  • International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)
  • System Usability Scale (SUS)
  • World Health Organization Quality of Life- BREF (WHOQOL-BREF)
10 weeks08 January 202612 February 20261
NCT07423949Using Non-invasive Brain and Spinal Cord Stimulation to Improve Arm and Hand Function After Spinal Cord InjuryUniversity of British Columbia
  • Age 19 - 75 yrs
  • Level C2-C8
  • AIS B, C, D
  • ≥ 12 months
  • NOT have any implanted metal (other than dental implants) in the skull or presence of pacemakers, stimulators, or medication pumps in the trunk
Recruiting soon24NATechnologyArm/hand function
  • Feasibility
  • Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
  • Magnetic Resonance Imaging (MRI) - conventional/anatomical and quantitative
  • Motor Evoked Potentials (MEPs)
8 weeks01 March 202620 February 20261
NCT07425470SCI Epidemiology and ComplicationsBandırma Onyedi Eylül University
  • Age All ages
  • Level C1-S5
  • AIS
  • All
Recruiting soon50General health1 month01 March 202620 February 20261
NCT07429188Impact Study on Users of Upper Limb Assistive DevicesAssociation APPROCHE
  • Age ≥ 18 yrs
  • Level C1-S5
  • AIS
  • All
Recruiting150Mental health and psychosocial factors
  • Canadian Occupational Performance Measure
  • European Quality of Life Five Dimension Five Level Scale (EQ-5D-5L)
  • Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST)
60 days12 February 202624 February 20262
NCT07438353Home-Based Digital Rehabilitation Program Optimized With Transcutaneous Spinal Cord Stimulation for Upper Limb Functional Enhancement in Tetraplegia (HOPE): A Safety, Efficacy, and Feasibility StudySingapore General Hospital
  • Age 21 - 75 yrs
  • Level C1-T1
  • AIS
  • ≥ 12 years
  • NOT have a pacemakers or other implantable stimulators
Recruiting soon9NATechnologyArm/hand function
  • Adverse Events (AEs)
  • Feasibility
  • Goal Attainment Scaling (GAS) score
  • Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
22 weeks01 April 202627 February 20261
NCT07440459Promoting Neuroplastic Mechanisms With Modeling-based Optimization of a Novel Robot-asisted Walking Rehabilitation TherapyBioRobotics Group - Spanish National Research Council (CSIC)
  • Age 18 - 80 yrs
  • Level C5-L1
  • AIS C, D
  • 2 months - 6 months
  • NOT have implanted electronic devices or metal implants in the skull
Ended10Standing/walking/mobility
  • 10 Meter Walking Test (10 MWT)
  • Ashworth and Modified Ashworth Scale (MAS)
  • International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI)
  • Motor Evoked Potentials (MEPs)
  • Pain Visual Analog Scale (VAS)
  • Surface Electromyography (sEMG)
  • Timed Up and Go Test (TUG)
  • Walking Index for Spinal Cord Injury (WISCI) and WISCI II
12 weeks12 June 202327 February 20261