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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04578080
Other study ID # SI284/2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 1, 2020
Est. completion date June 1, 2022

Study information

Verified date June 2022
Source Mahidol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aims to investigate the effects of anodal tDCS combined with conventional physical therapy for 5 consecutive sessions on motor functions and brain activity in acute stroke patients at immediate and 1-month follow-up.


Description:

Stroke or cerebrovascular accident is a leading cause of disabilities. Physical therapy is a standard treatment to help motor recovery after stroke. However, disabilities remained in some stroke patients despite intensive training. After stroke, there are changes of cortical excitability and brain activity in both hemispheres. Lesioned hemisphere decreases cortical excitability and increases number of low-frequency brain activity, while the non-lesioned hemisphere increases cortical excitability and increases number of high-frequency brain activity. Transcranial direct current stimulation (tDCS) is a technique which delivers weak direct current through scalp and can be used as an adjunctive treatment. Anodal tDCS can increase cortical excitability and amount of high-frequency brain activity. Increased amount of high-frequency brain activity in the lesioned hemisphere can indicate better recovery of stroke. Meta-analysis has reported the benefits of anodal tDCS for motor recovery in stroke patients. However, only few studies have investigated tDCS effects in acute phase of stroke which is a crucial time for enhancing motor recovery. This study aims to investigate the effects of anodal- and cathodal tDCS combined with conventional physical therapy for 5 consecutive sessions on motor functions and brain activity in acute stroke patients at immediate and 1-month follow-up. Participants will be randomly assigned into 2 groups (sham-, and anodal tDCS). Participants in the anodal group will receive 1.5 mA tDCS for 20 minutes before physical therapy programs for 5 consecutive sessions, while the sham group will receive sham tDCS with physical therapy. Brain activity by electroencephalography and motor performances by Fugl-Meyer Assessment and Wolf Motor Function Test will be evaluated at baseline, post-intervention (day 5), and follow-up at 1 month. We hypothesize that anodal tDCS combined with physical therapy for 5 consecutive days can immediately increase number of high-frequency brain activity and improve motor functions and this effect will last for a month compared to the sham group.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 1, 2022
Est. primary completion date June 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: 1. Age between 18-75 years old 2. First-ever acute ischemic stroke of anterior circulation system (anterior cerebral artery or middle cerebral artery territory) 3. Stroke onset from 2-10 days 4. Having a stable medical condition 5. Alert of consciousness 6. Able to follow commands 7. Modified Rankin Scale (mRS) = 4 Exclusion Criteria: 1. Hemorrhagic stroke 2. Recurrent stroke 3. Presence of other neurological disorders such as unilateral neglect 4. Presence of metal implantation, intracranial shunt, cochlear implantation or cardiac pacemakers 5. Presence of opened wound or infectious wound around scalp 6. History of epilepsy or any neurological antecedent or unstable condition which can lead to seizure 7. Body Mass Index (BMI) > 30 kg/m2 8. Received hormonal treatment 9. Ischemic heart disease and peripheral vascular ischemia 10. Last stage of kidney disease and liver disease

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Transcranial direct current stimulation
Anodal or Sham tDCS will be applied in 1.5 mA, 20 mins before conventional physical therapy for 5 days. All experiments will be performed in random order for each subject.

Locations

Country Name City State
Thailand Siriraj Hospital Bangkok Noi Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Mahidol University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Other Wolf Motor Function Test Two sub-items (lift a can and lift a pencil) will be evaluated in all participants. 5 minutes
Primary Electroencephalography Brain activity will be recorded during eyes open (5 minutes) follow by eyes close (5 minutes). 10 minutes
Secondary Fugl-Meyer Assessment The gold standard and widely used tool to assess sensorimotor in stroke. The item from upper limb and lower limb section will be used. The items are rated on a 3-point ordinal scale as follows: 0 = unable to perform; 1 = partial ability to perform; and 2 = near normal ability to perform. 20 minutes
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