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Clinical Trials/NCT02393651
NCT02393651
Unknown
Not Applicable

Late LTP-like Plasticity Effects of tDCS in Subacute Stroke Patients

Erasmus Medical Center1 site in 1 country48 target enrollmentMarch 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
Erasmus Medical Center
Enrollment
48
Locations
1
Primary Endpoint
Change from baseline in Upper Extremity Fugl Meyer Assessment
Last Updated
7 years ago

Overview

Brief Summary

Rationale: About 80% of stroke patients suffer motor impairments, but current therapies have limited effects on motor recovery. Therefore, investigating new potential therapeutic approaches is crucial. Transcranial Direct Current Stimulation (tDCS) is a form of non-invasive electrical stimulation where a weak current is applied through electrodes over the scalp. This stimulation is known to (1) induce changes in neuronal excitability -which can last up to one day with late LTP-like plasticity protocols in a polarity and site-specific manner, and (2) facilitate motor learning and stroke recovery. So far, several pilot studies have reported beneficial results from tDCS in both subacute and chronic stroke patients, but it's still unclear how tDCS should be repeated over multiple days to optimally enhance recovery and training effects. Using a late LTP-like plasticity protocol could increase effectiveness of standard clinical care rehabilitation sessions and thus enhance the effects of rehabilitation. Therefore, the investigators want to investigate how late LTP-like plasticity tDCS affects rehabilitation in subacute stroke patients. The outcome of this study can provide important guidelines on effective motor therapy during stroke rehabilitation.

Objective: Identify the effect of late LTP-like plasticity on motor rehabilitation during the subacute phase after stroke.

Study design: Double-blinded, randomized between-subjects trials. Study population: Subacute stroke patients. Main study parameters/endpoints: The primary outcome measure is the upper limb motor function during the subacute phase after stroke.

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
May 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rick van der Vliet

MSc

Erasmus Medical Center

Eligibility Criteria

Inclusion Criteria

  • Subacute stroke (within 1-4 weeks post stroke)
  • Acute hemiparesis (Fugl-Meyer Stage \< IV) with single thromboembolic non-hemorrhagic infarction documented by a neurologist
  • Aged 18-79

Exclusion Criteria

  • Absence of voluntary movement (Fugl-Meyer Stage \< III)
  • Head injury or the presence of intracranial metal or intracranial lesions
  • History of cranial irradiation
  • History of epilepsy
  • Presence of a pacemaker
  • Taking anticonvulsant or neuroleptic medication
  • Substance abuse
  • Inability to understand instructions

Outcomes

Primary Outcomes

Change from baseline in Upper Extremity Fugl Meyer Assessment

Time Frame: Baseline, 1 week, 2 weeks, 4 weeks and 12 weeks

Secondary Outcomes

  • ARAT(Baseline, 1 week, 2 weeks, 4 weeks and 12 weeks)
  • Hand grip strength(Baseline, 1 week, 2 weeks, 4 weeks and 12 weeks)
  • 10-meter walk test(Baseline; 1 week, 2 weeks, 4 weeks and 12 weeks)
  • EuroQol-5D(12 weeks)
  • Barthel Index(Baseline; 1 week, 2 weeks, 4 weeks and 12 weeks)
  • HADS(Baseline; 4 weeks and 12 weeks)
  • MoCA(Baseline; 4 weeks and 12 weeks)
  • Wong-Baker FACES Pain Rating Scale(Every stimulation session)

Study Sites (1)

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