N/A
Completed N=17
To Determine the Therapeutic Effect of the Music Glove and Conventional Hand Exercises to Subacute Stroke Patients
Cerebrovascular Accident
Source: ClinicalTrials.gov NCT02410629 ↗
Enrolled (actual)
17
Serious AEs
0.0%
Results posted
Apr 2020
Primary outcomePrimary: Box and Block Test — 21; 33; 12; 7 blocks
Summary
The investigators are trying to determine the therapeutic effect of the music glove and conventional hand exercise program to the subacute stroke patients. 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 a minimal 3 hours exercise time per week. Participants will receive the other intervention at 3-month post stroke date. Clinical evaluations will be performed at baseline, post therapy after first intervention, 3-week post intervention follow up, 3-month post stroke, post therapy after second intervention, 3-week post second intervention follow up, and 6-month post stroke follow up visits.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Box and Block Test |
21; 33; 12; 7; 19; 12 | — |
| SECONDARY Fugl-Meyer Motor Assessment of the Upper Extremity |
44; 42; 4; 7; 9; 9 | — |
| SECONDARY Action Research Arm Test |
42; 47; 9; 7; 13; 7 | — |
| SECONDARY 9-Hole Peg Test |
55; 47; -5; -7; -9; -5 | — |
Eligibility Criteria
Inclusion Criteria
- History of a single stroke at least 1 week prior to enrollment
- Upper Extremity weakness measured on a standard clinical scale
- No active major psychiatric problems, or neurological/orthopedic problems affecting the stroke affected upper extremity
- No active major neurological disease other than the stroke
- 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 aphasia as measured on a standard clinical scale
- Severe reduced level of consciousness
- Severe sensory/proprioception deficit at the affected upper extremity as measured on a standard clinical scale
- Currently pregnant
- 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 affected upper extremity
Data sourced from ClinicalTrials.gov (NCT02410629). 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.