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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01781689
Other study ID # VGHKS102-086
Secondary ID VGHKS12-CT7-07
Status Completed
Phase N/A
First received
Last updated
Start date October 2012
Est. completion date August 1, 2019

Study information

Verified date October 2023
Source Kaohsiung Veterans General Hospital.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Stroke is the most common cause of motor function impairment. However, the functional impairment is not totally irreversible. Several mechanisms may involved in both the cortical and motor function recovery after onset of stroke, and most of them are related to changes of cortical perfusion and metabolism. Motor function recovery after stroke (especially middle cerebral artery territory lesion) frequently follow stereotypic pattern (brunnström stage). This study is designed to investigate the relationship between motor cortex oxygenation/metabolism and motor function recovery after stroke. To seek if there is similar stereotypic pattern of motor cortex oxygenation/metabolism change during the recover stage after stroke.


Description:

Participants receive evaluations (1/week for 3 months period) of - motor function (Include: MMSE, brunnström stage, Fugl-Meyer Assessment of Physical Performance, Box and Block Test of Manual Dexterity, Functional Independence Measure) - cortical perfusion detection during performing limb movements (using NIRS) Then use path analysis to investigate the relationship between motor cortex oxygenation/metabolism and motor function recovery after stroke.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date August 1, 2019
Est. primary completion date July 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 80 Years
Eligibility Inclusion Criteria: - Ischemic stroke(unilateral, onset within 7 days, without previous stroke history) - Vital sign stable - Upper extremity motor function impairment(brunnström stage I~III) Exclusion Criteria: - with pacemakers - Seizure history - Serious dysrhythmias - Poor cognition function(MMSE<13)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Functional Electric Stimulation
apply to the hemiplegia affected limbs, helping movement
Other:
Rehabilitation programs
include occupational therapy and physical therapy

Locations

Country Name City State
Taiwan Kaohsiung Veterans General Hospital Kaohsiung

Sponsors (1)

Lead Sponsor Collaborator
Kaohsiung Veterans General Hospital.

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Other Activity of daily living function assess Activity of daily living function weekly for 3 months weekly changes within 3 months
Primary Cortical activation Using Near-infrared spectroscopy to measure cortical activation changes weekly for 3 months weekly changes within 3 months
Secondary motor function assess motor function every week for 3 months weekly changes within 3 months
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