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

Sponsor
Medical University of South Carolina (Other)
Overall Status
Terminated
CT.gov ID
NCT02892097
Collaborator
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
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Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Device: tDCS
  • Device: sham tDCS
  • Behavioral: Repetitive task-specific practice (RTP)
Phase 1

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
1 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Examining the Effects of Transcranial Direct Current Stimulation and Task-specific Practice on Cortical Modulation Among Individuals With Unilateral Spatial Neglect Post Stroke
Actual Study Start Date :
Jul 1, 2016
Actual Primary Completion Date :
Nov 7, 2017
Actual Study Completion Date :
Nov 7, 2017

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Parietal tDCS plus RTP

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

Device: 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.
Other Names:
  • noninvasive brain stimulation
  • transcranial direct current stimulation
  • Behavioral: Repetitive task-specific practice (RTP)
    Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.
    Other Names:
  • task practice
  • Active Comparator: 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)

    Device: 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.
    Other Names:
  • noninvasive brain stimulation
  • transcranial direct current stimulation
  • Behavioral: Repetitive task-specific practice (RTP)
    Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.
    Other Names:
  • task practice
  • Sham Comparator: Sham tDCS plus RTP

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

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

    Behavioral: Repetitive task-specific practice (RTP)
    Participants will practice using their paretic arm/hand to complete functional movements during each (3) 30 minute training session.
    Other Names:
  • task practice
  • Outcome Measures

    Primary Outcome Measures

    1. Change in excitability of fronto-parietal connectivity [Participants will be assessed at baseline and 30 minutes later (immediately following intervention session).]

      Excitability of fronto-parietal connectivity measured by paired pulse twin coil transcranial magnetic stimulation (TMS) test. In each session, the difference in excitability of fronto-parietal connectivity between pre and post stimulation will be measured.

    Secondary Outcome Measures

    1. Change in kinematics [Participants will be assessed at baseline and 1 hour later (immediately following intervention session).]

      A kinematic assessment will be conducted to assess changes in motor impairment.

    2. Change on Behavioral Inattention Test [Participants will be assessed at baseline and 1.5 hours later (immediately following intervention session).]

      A neglect assessment will be conducted to assess changes in attentional impairment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Medical University of South Carolina Charleston South Carolina United States 29425

    Sponsors and Collaborators

    • Medical University of South Carolina
    • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    Investigators

    • Principal Investigator: Emily Grattan, PhD, OTR/L, Medical University of South Carolina

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Medical University of South Carolina
    ClinicalTrials.gov Identifier:
    NCT02892097
    Other Study ID Numbers:
    • PRO00056688
    • P2CHD086844
    First Posted:
    Sep 8, 2016
    Last Update Posted:
    Sep 13, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by Medical University of South Carolina
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 13, 2021