Transcranial Direct Current Stimulation (tDCS) and Task-Specific Practice for Post-stroke Neglect

NCT ID: NCT02892097

Last Updated: 2021-09-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE1

Total Enrollment

1 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-31

Study Completion Date

2017-11-07

Brief Summary

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The purpose of this study is to test the effects of three different rehabilitation training sessions that combine non-invasive brain stimulation (transcranial direct current stimulation, tDCS) with arm rehabilitation training (repetitive task-specific practice, RTP) for individuals with unilateral spatial neglect following stroke. This study is designed to determine the effects of tDCS + RTP on the excitability in the brain, attention to the affected side, and arm movement ability.

Detailed Description

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Unilateral neglect (neglect) is common after stroke and is characterized by an inattention to one side of the body or environment. There is growing evidence that disconnections to fronto-parietal neural networks in the lesioned hemisphere not only cause neglect, but also cause these same networks to be hyperexcited in the non-lesioned hemisphere. Individuals with neglect typically experience motor impairments also since the regions of the brain that control attention also control movement.

Transcranial direct current stimulation (tDCS) when paired with repetitive task-specific practice (RTP) has the potential to modulate cortical activity (fronto-parietal networks) and facilitate motor and attentional recovery for individuals with neglect since tDCS can modulate the excitability of targeted cortical regions. tDCS is a form on non-invasive brain stimulation and RTP is the gold standard post-stroke motor recovery intervention.

It is particularly important investigators examine the effect of RTP + tDCS on cortical modulation in order to understand the underlying mechanism of the intervention and determine whether RTP+ tDCS (parietal or primary motor cortex \[M1\]) promotes greater neural modulation than RTP alone. Traditionally, electrodes are placed on M1 to facilitate motor recovery and on the parietal lobe to facilitate attentional recovery, however this intervention is designed to target each of these impairments (motor, attention) and enhance cortical modulation of fronto-parietal networks. Therefore, investigators must also determine the optimal electrode montage and placement for pairing tDCS with RTP for individuals with neglect.

The purpose of the proposed pilot project is to examine the effects of transcranial direct current stimulation (tDCS) paired with repetitive task-specific practice (RTP) on modulation of fronto-parietal network connectivity (measured by transcranial magnetic stimulation \[TMS\]), motor impairment (measured with kinematic assessment), and attentional impairment (measured with Behavioral Inattention Test) among individuals with unilateral neglect and hemiparesis post stroke. This three day cross-over design study will examine the optimal electrode placement and montage using 3 conditions: (1) tDCS to parietal lobe + RTP (2) tDCS to primary motor cortex + RTP (3) sham tDCS + RTP.

Conditions

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Stroke Hemispatial Neglect

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Parietal tDCS plus RTP

Single session of bilateral parietal tDCS (2.0 mA for 30 minutes) paired with repetitive task-specific practice (RTP).

Group Type ACTIVE_COMPARATOR

tDCS

Intervention Type DEVICE

tDCS is a form of noninvasive brain stimulation. Electrodes are placed on the scalp (parietal or primary motor cortex) and deliver a low level of direct current (2mA). tDCS will be delivered for 30 minutes in conjunction with repetitive task-specific practice for the arm/hand.

Repetitive task-specific practice (RTP)

Intervention Type BEHAVIORAL

Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.

Primary motor cortex tDCS plus RTP

Single session of bilateral primary motor cortex tDCS (2.0 mA for 30 minutes) paired with repetitive task-specific practice (RTP)

Group Type ACTIVE_COMPARATOR

tDCS

Intervention Type DEVICE

tDCS is a form of noninvasive brain stimulation. Electrodes are placed on the scalp (parietal or primary motor cortex) and deliver a low level of direct current (2mA). tDCS will be delivered for 30 minutes in conjunction with repetitive task-specific practice for the arm/hand.

Repetitive task-specific practice (RTP)

Intervention Type BEHAVIORAL

Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.

Sham tDCS plus RTP

Single session of sham tDCS (for 30 minutes) paired with repetitive task-specific practice (RTP)

Group Type SHAM_COMPARATOR

sham tDCS

Intervention Type DEVICE

Sham tDCS will be delivered for 30 minutes in conjunction with repetitive task-specific practice for the arm/hand.

Repetitive task-specific practice (RTP)

Intervention Type BEHAVIORAL

Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.

Interventions

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tDCS

tDCS is a form of noninvasive brain stimulation. Electrodes are placed on the scalp (parietal or primary motor cortex) and deliver a low level of direct current (2mA). tDCS will be delivered for 30 minutes in conjunction with repetitive task-specific practice for the arm/hand.

Intervention Type DEVICE

sham tDCS

Sham tDCS will be delivered for 30 minutes in conjunction with repetitive task-specific practice for the arm/hand.

Intervention Type DEVICE

Repetitive task-specific practice (RTP)

Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.

Intervention Type BEHAVIORAL

Other Intervention Names

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noninvasive brain stimulation transcranial direct current stimulation task practice

Eligibility Criteria

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Inclusion Criteria

* Unilateral hemispheric ischemic stroke or hemorrhagic subcortical stroke ≥3 months post stroke (lesion type and location to be confirmed with MRI)
* Neglect (Virtual Reality Lateralized Attention Test score \<18)
* Upper extremity Fugl-Meyer score between 20-56/60
* Inducible motor evoked potential (MEP) of the abductor pollicis brevis (APB) on the affected side using transcranial magnetic stimulation (TMS)
* ≥18 years old

Exclusion Criteria

* History of cortical hemorrhagic stroke
* Severe spasticity (Modified Ashworth Scale score ≥3) in paretic upper extremity
* Severe aphasia limiting participant's ability to follow 2 step directions
* History of seizures
* History of brain tumor
* History of skull defect
* Hardware in skull or spine (e.g. coils, clips)
* Implantable medical device (e.g. pacemaker)
* Metal in body that is not compatible with MRI
* Pregnant (women of child bearing age will be asked if they are pregnant or could possibly be pregnant)
* Unable to travel to Upper Extremity Motor Function Laboratory at the Center for Rehabilitation Research in Neurological Conditions
* Currently enrolled in another study using transcranial direct current stimulation (tDCS) or transcranial magnetic stimulation (TMS)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

Sponsor Role collaborator

Medical University of South Carolina

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Emily Grattan, PhD, OTR/L

Role: PRINCIPAL_INVESTIGATOR

Medical University of South Carolina

Locations

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Medical University of South Carolina

Charleston, South Carolina, United States

Site Status

Countries

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United States

Other Identifiers

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P2CHD086844

Identifier Type: NIH

Identifier Source: secondary_id

View Link

PRO00056688

Identifier Type: -

Identifier Source: org_study_id

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