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N/A N=13 Single-blind Device Feasibility

Cognitive-based Prosthetics to Improve Grasp and Reaching After SCI

Spinal Cord Injuries · Hand Weakness

Enrolled (actual)
13
Serious AEs
0.0%
Results posted
Apr 2025
Primary outcome: Primary: Percent Change in Time to Achieve Secure Grasp (Cognition Glove Only) — 39.9; -14.6; 10.1 % change in time to secure grasp

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Cognition glove (Device); Sensory brace (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Oct 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Percent Change in Time to Achieve Secure Grasp (Cognition Glove Only)
39.9; -14.6; 10.1
PRIMARY
Percent Change in Time to Complete Pick-up and Placement of Object-Cognition Glove
20.2; 7.9; -24.4
PRIMARY
Percent Change in Time to Complete Trial-Sensory Brace
18.6; 3.3
SECONDARY
Percent Change in Motion Pathlength in Moving Object-Cognition Glove
39.1; 21.9; -12.4
SECONDARY
Percent Change in Motion Pathlength Toward Virtual Targets-Sensory Brace
17.7; 1.4
SECONDARY
Error in Placing Object Onto Target (Cognition Glove Only)
0; 0; 0

Summary

Rehabilitation of functional movements after spinal cord injury (SCI) requires commitment and engagement to the processes of physical therapy. Outcomes may be improved by techniques that strengthen cognitive connections between users and physical therapy exercises. The investigators will investigate combinations of virtual reality and innovative wearable technology to accelerate rehabilitation of hand grasp and reach. These devices use multi-sensory feedback to enhance the sense of agency, or feelings of control, and better train movements during physical rehabilitation exercises. The investigators will measure the effect of these devices on improving the speed, efficiency, and accuracy of performed movements in Veterans with SCI.

Eligibility Criteria

Inclusion Criteria

  • SCI occurred greater than 12 months ago
  • SCI occurred between levels C1-T1
  • Hand weakness: score of 2, 3, or 4 out of 5 on manual muscle testing of finger extension, finger flexion, or finger abduction in either hand

Exclusion Criteria

  • History of other serious brain or spinal cord injuries
  • History of seizures
  • Ventilator dependence; open tracheostomy
  • Use of medications that significantly lower seizure threshold
  • History of significant cognitive deficits
  • Open skin lesions over the face, neck, shoulders, arms, or hands
  • Pregnancy
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04577573). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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