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Effects of Upper Extremity Rehabilitation Robot and Transcranial Direct Current Stimulation in Chronic Stroke

Effects of Upper Extremity Rehabilitation Robot and Transcranial Direct Current Stimulation on Upper Extremity Function Among Subjects With Chronic Stroke

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04005131
Enrollment
20
Registered
2019-07-02
Start date
2018-05-01
Completion date
2019-12-31
Last updated
2019-07-02

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

Conditions

Stroke

Keywords

stroke, transcranial direct current stimulation, upper extremity rehabilitation robot

Brief summary

Comparison of real transcranial direct current stimulation (tDCS) and sham tDCS combined with robot training for upper extremity rehabilitation in subjects with chronic stroke - delayed start study.

Interventions

Combined transcranial direct current stimulation(tDCS) on-line and upper extremity rehabilitation robot for 5 times a week for 10 weeks

DEVICERobot and tDCS on-line after sham tDCS

Combined sham tDCS and upper extremity rehabilitation robot for 5 times a week for 5 weeks, followed by combined tDCS on-line and upper extremity rehabilitation robot for 5 times a week for 5 weeks

Sponsors

National Rehabilitation Center, Seoul, Korea
Lead SponsorOTHER_GOV

Study design

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

Masking description

Participant does not know the allocation.

Eligibility

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

Inclusion criteria

* Hemiplegic patients secondary to first cerebrovascular accidents * Onset ≥ 6 months * Fugl-Meyer Assessment score ≥ 19 * Cognitively intact enough to understand and follow the instructions from the investigator

Exclusion criteria

* Severe upper extremity pain that could interfere with rehabilitation therapy * Neurological disorders other than stroke that can cause motor deficits * Uncontrolled severe medical conditions.

Design outcomes

Primary

MeasureTime frameDescription
kinematic data during scale for the assessment5 weeks after baselinekinematic data during scale for the assessment and rating of ataxia using Trakstar (mean velocity, jerk, smoothness)

Secondary

MeasureTime frameDescription
kinematic data during scale for the assessmentbaseline, 1 weeks after baseline, 5 weeks after baseline, 6 weeks after baseline, 10 weeks after baselinekinematic data during scale for the assessment and rating of ataxia using Trakstar (mean velocity, jerk, smoothness)
Fugl-Meyer Assessment - upper extremitybaseline, 1 weeks after baseline, 5 weeks after baseline, 6 weeks after baseline, 10 weeks after baselineindicator of the level of impairment of upper extremity, with higher scores indicating lower impairment
Wolf Motor Function Testbaseline, 1 weeks after baseline, 5 weeks after baseline, 6 weeks after baseline, 10 weeks after baselinean activity indicator, has 15 items for testing functional ability
Motor activity logbaseline, 1 weeks after baseline, 5 weeks after baseline, 6 weeks after baseline, 10 weeks after baselineAssesses the use of the paretic arm and hand during activities of daily living in hemiparetic stroke patients.
Action reach arm testbaseline, 1 weeks after baseline, 5 weeks after baseline, 6 weeks after baseline, 10 weeks after baselineto assess upper extremity performance (coordination, dexterity and functioning) in stroke recovery

Countries

South Korea

Contacts

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

Outcome results

None listed

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