Skip to content

Effectiveness of MusicGlove and FitMi training in subacute stroke patient: A randomized controlled trial

Effectiveness of MusicGlove and FitMi training in subacute stroke patient: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
TCTR
Registry ID
TCTR20211102005
Enrollment
28
Registered
2021-11-02
Start date
2021-11-16
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

rehabilitation for upper extremities in subacute unilateral stroke patients upper extremities rehabilitation unilateral stroke subacute stroke

Interventions

1 hour of intervention program per day for 3 days per week for 4 weeks (Total 12 sessions). The program will consist of ROM exercise of finger and wrist for 15 minutes and 45 minutes of MusicGlove and
Experimental Device,Active Comparator Device
MusicGloves and FitMi,Control group (Conventional therapy)

Sponsors

Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 Age between 18 - 80 years old 2 No active neurological disease other than stroke 3 First-ever subacute stroke onset from 2 weeks to 6 months 4 Unilateral weakness 5 Mild to moderate impairment of upper extremity after stroke categorized by BBT>=1 , ARAT 11-42 points

Exclusion criteria

Exclusion criteria: 1 Unstable medical or neurological condition 2 Difficulty in understanding or TMSE < 23 3 Severe neglect 4 Severe aphasia 5 Severe visual impairment 6 Spasticity of upper extremities; Modified Ashworth's Scale >=2 7 Severe limit range of upper extremity motion 8 Pain (VRS > 4) or other orthopedic problem on stroke-affected upper extremity 9 Unable to sit upright more than 30 minutes 10 Receiving any other rehabilitation treatment than conventional therapy within 3 months

Design outcomes

Primary

MeasureTime frame
Manual gross dexterity of unilateral upper extremity At the end of program and 4 weeks after the end of treatment Box and Block Test (BBT)

Secondary

MeasureTime frame
function of upper extremity at the end of program and 4 weeks after the end of treatment Action Research Arm Test (ARAT)

Countries

Thailand

Contacts

Public ContactMarisa Supradit Na Ayuttaya

Department of Rehabilitation Medicine, Faculty of Medicine, Chulalongkorn University

carrotkun@gmail.com0863889291

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026