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Upper Extremity Rehabilitation Using Game Rehabilitation System With Functional Electrical Stimulation for Stroke Patients

Upper Extremity Rehabilitation Using Game-based Virtual Reality Rehabilitation System (Smart Glove System) With Functional Electrical Stimulation for Stroke Patients : Randomized Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02772510
Enrollment
54
Registered
2016-05-13
Start date
2015-02-28
Completion date
2016-10-31
Last updated
2016-10-25

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

Conditions

Stroke

Keywords

Stroke, Rehabilitation, Hand, Game, Functional electrical stimulation, Virtual reality

Brief summary

The purpose of the present study was to investigate the effects of game-based virtual reality rehabilitation combined with functional electrical stimulation on distal upper extremity function, and compare the findings to those of functional electrical stimulation in stroke survivors.

Interventions

DEVICEFunctional electrical stimulation

Functional electrical stimulation on distal upper extremity

DEVICESmart glove system with functional electrical stimulation

Game-based virtual reality rehabilitation system (Smart glove system) combined with functional electrical stimulation on distal upper extremity

Sponsors

National Rehabilitation Center, Seoul, Korea
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* first-ever ischemic or hemorrhagic stroke * wrist extensor of medical research council scale 1\ 3 * No clinical evidence of limited passive range of motion of affected wrist

Exclusion criteria

* age \<18 years * severe aphasia resulting in communication difficulties confounding intervention and outcome measures * severe cognitive impairment resulting cooperation difficulties * spasticity \> modified Ashworth scale 1+

Design outcomes

Primary

MeasureTime frame
Wolf Motor Function Test4 weeks from baseline
Fugl-Meyer Assessment-hand & wrist4 weeks from baseline

Secondary

MeasureTime frameDescription
Fugl-Meyer Assessment upper extremitybaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baselineglobal assessment of upper extremity impairment
Stroke Impact Scalebaseline, 4 weeks after baseline
Motor Activity Logbaseline, 4 weeks after baseline
Medical research council scale of elbow flexion/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Medical research council scale of wrist flexion/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Range Of Motion of elbow flexion/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Range Of Motion of wrist flexion/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Wolf Motor Function Testbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Jebsen-Taylor hand function testbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Modified Ashworth scale of elbow flexor/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Modified Ashworth scale of wrist flexion/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Modified Tardieu scale of elbow flexor/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Modified Tardieu scale of wrist flexion/extensionbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Adverse eventsbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baselineAny adverse events
Brunnstrom stagebaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baselineIt represent the recovery status among stroke patients
Box and Block Testbaseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baselinenumber of block transferred by hand from one box to other box.

Countries

South Korea

Contacts

Primary ContactJoon-Ho Shin, MS
asfreelyas@gmail.com82-2-901-1884

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026