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N/A Completed N=11 Randomized Single-blind Treatment

Efficacy Study of the Music Glove Patients With Spinal Cord Injuries

Spinal Cord Injuries
Source: ClinicalTrials.gov NCT02473614 ↗
Enrolled (actual)
11
Serious AEs
0.0%
Results posted
Jun 2021
Primary outcomePrimary: Box and Blocks Test — 40.6; 40; 44.8; 39.0 blocks

Summary

Investigators are trying to determine the therapeutic effect of the music glove and conventional hand exercise program to patients with spinal cord injuries. All participants will be randomized into two groups: AB and BA. They will all exercise at least 3 times a week for 3 weeks with minimum of 3 hours of exercise time per week. Participants will receive the other intervention at their 3 week post-therapy follow-up visits. Clinical evaluations will be performed at baseline 1 and 2 (3 to 10 days apart), post-therapy after the first intervention, 3-week post-therapy follow up, post-therapy after the second intervention, and 3-week post-second intervention follow up visits.

Outcome Measures

OutcomeResultp-value
PRIMARY
Box and Blocks Test
40.6; 40; 44.8; 39.0; 46.4; 41.0
SECONDARY
Graded Redefined Assessment of Strength, Sensibility and Prehension (GRASSP)
18.6; 18.6; 20.0; 19.0; 19.6; 20.6

Eligibility Criteria

Inclusion Criteria

  • History of spinal cord injury affecting the arm and hand functions, at least 6 months prior to enrollment
  • Upper extremity weakness as measured on a standard clinical scale
  • No active major psychiatric problems, or neurological/orthopedic problems affecting the training upper extremity
  • No active major neurological disease other than the spinal cord injury
  • Absence of pain in the affected upper extremity

Exclusion Criteria

  • Severe tone at the affected upper extremity as measured on a standard clinical scale
  • Severe sensory/proprioception deficit at the affected upper extremity as measured on a standard clinical scale
  • Difficulty in understanding or complying with instructions given by the experimenter
  • Inability to perform the experimental task that will be studied
  • Increased pain with movement of the training upper extremity
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02473614). 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. Informational only — not medical advice.

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