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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04451941
Other study ID # NRC-2020-01-007
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date December 31, 2021

Study information

Verified date July 2020
Source National Rehabilitation Center, Seoul, Korea
Contact Joon-Ho Shin
Phone 82-2-901-1884
Email asfreelyas@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Determination of clinical effects of brain machine interface in chronic stroke patient without wrist extensor strength


Description:

The purpose of this study is to compare RecoveriX with individual EEG calibration and without individual EEG calibration to determine the clinical effect of brain machine interface in chronic stroke patient without wrist extensor strength


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 31, 2021
Est. primary completion date December 1, 2021
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

- Hemiplegic patients secondary to first cerebrovascular accidents

- Weak wrist extension

- Onset = 6 months

- Fugl-Meyer Assessment score = 19

- Cognitively intact enough to understand and follow the instructions from the investigator

Exclusion Criteria:

- Wrist extensor spasticity above or modified ashworth scale 2

- Severe upper extremity pain that could interfere with rehabilitation therapy

- Neurological disorders other than stroke that can cause motor deficits

- Uncontrolled severe medical conditions.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Experimental: RecoveriX with individual EEG calibration
RecoveriX applied FES according to individual brainwave by individual EEG calibration for 5 times a week for 4 weeks
RecoveriX without individual EEG calibration
RecoveriX applied FES according to the brainwave of other subjects regardless of the individual brainwave for 5 times a week for 4 weeks

Locations

Country Name City State
Korea, Republic of National Rehabilitation Center Seoul

Sponsors (1)

Lead Sponsor Collaborator
National Rehabilitation Center, Seoul, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fugl-Meyer Assessment - upper extremity Fugl-Meyer Assessment is indicator of the level of impairment of upper extremity, with higher scores indicating lower impairment.
Total scores range from 0 to 66, each item being scored on a 3-point scale (0, cannot perform; 1, partially performs; and 2, fully performs the task).
4 weeks after baseline
Secondary Box and block test Box and block test measures unilateral gross manual dexterity. Higher scores indicate better gross manual dexterity. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Jebsen hand function test Jebsen hand function test provides a standardized and objective evaluation of fine and gross motor hand function using simulated activities of daily living. Total score is the sum of time taken for each subtest, which are rounded to the nearest second. Shorter times indicate better performance. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary 9-hole peg test 9-hole peg test measures finger dexterity in patients with stroke. Scores are based on the time taken to complete the test activity, recorded in seconds. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Medical Research Council (MRC) scale of affected upper extremity The MRC is a standardized set of assessments that measure muscle strength and function.
The MRC scale of muscle strength uses a score of 0 to 5 to grade the power of a particular muscle group in relation to the movement of a single joint.
baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Joint position sense Joint position sense is tested by holding the most distal joint of a digit by its sides and moving it slightly up or down. First, demonstrate the test with the patient watching so they understand what is wanted then perform the test with their eyes closed. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Sensation of limb movement For the ability to sense a sharp object, the best screening test uses a safety pin or other sharp object to lightly prick the face, torso, and 4 limbs; the patient is asked whether the pinprick feels the same on both sides and whether the sensation is dull or sharp. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary active range of motion (AROM) of wrist flexion/extension active range of motion of wrist flexion and extension baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Modified Ashworth scale Modified Ashworth scale measures resistance during passive soft-tissue stretching.
Scores range from 0-4, with 5 choices. A score of 1 indicates no resistance, and 5 indicates rigidity.
baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Stroke impact scale Stroke impact scale evaluates how stroke has impacted your health and life. Each item is rated in a 5-point Likert scale in terms of the difficulty the patient has experienced in completing each item. Summative scores are generated for each domain, scores range from 0-100. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary electroencephalography (EEG) effective connectivity EEG effective connectivity describes the causal influences that neural units exert over another. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Stroke rehabilitation motivation scale Stroke rehabilitation motivation scale includes 28 items applicable to stroke rehabilitation, adapted from the Sports Motivation Scale. The response to each item is measured on a scale of 1 to 5. Higher score indicates higher rehabilitation motivation level for all items, except three reverse evaluation items (items #5, #12, and #23), for which a higher score indicates lower motivation level. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Intrinsic motivation inventory The Intrinsic Motivation Inventory assesses participants' interest/enjoyment, perceived competence, effort, value/usefulness, felt pressure and tension, and perceived choice while performing a given activity, thus yielding six subscale scores. A higher score will indicate more of the concept described in the subscale name. baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
Secondary Motor evoked potential action potential elicited by noninvasive stimulation of the motor cortex through the scalp baseline, 2 weeks after baseline, 4 weeks after baseline, 8 weeks after baseline
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