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Clinical Trials/NCT01503073
NCT01503073
Suspended
Not Applicable

Noninvasive Brain Stimulation for Stroke Improvement

University Hospital of Mont-Godinne1 site in 1 country200 target enrollmentJanuary 2008
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
University Hospital of Mont-Godinne
Enrollment
200
Locations
1
Primary Endpoint
change in function before/after tDCS
Status
Suspended
Last Updated
2 years ago

Overview

Brief Summary

Noninvasive brain stimulations will be used in acute and chronic stroke patients to improve a variety of functions.

Detailed Description

Noninvasive brain stimulations (NIBS) will be used in acute and chronic stroke patients to improve a variety of functions such as motor functions, cognitive functions, ... NIBS will be applied in a placebo-controlled, double-blind, randomised fashion. Behavioural data will be collected before and after NIBS, as well as brain functional imaging data.

Registry
clinicaltrials.gov
Start Date
January 2008
End Date
December 2030
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University Hospital of Mont-Godinne
Responsible Party
Principal Investigator
Principal Investigator

Pr Yves Vandermeeren, MD, PhD

Professor, MD, PhD

University Hospital of Mont-Godinne

Eligibility Criteria

Inclusion Criteria

  • stroke with at least slight deficit

Exclusion Criteria

  • contraindication to tDCS and/or to fMRI
  • presence of metal in the head
  • unability to understand / complete behavioural tasks
  • chronic intake of alcohol or recreative drugs
  • major health condition
  • presence of pacemaker
  • pregnancy

Outcomes

Primary Outcomes

change in function before/after tDCS

Time Frame: Before intervention, immediately after intervention, 10-20-30-40-50-60 min after intervention; long-term after intervention : 1-2-3-4 weeks, 2-3-4-5-6-7-8-9-10-11-12 months

any brain function impaired by stroke

Secondary Outcomes

  • change in neuroimaging and neurophysiological before/after tDCS(Before intervention, immediately after intervention, 10-20-30-40-50-60 min after intervention; long-term after intervention : 1-2-3-4 weeks, 2-3-4-5-6-7-8-9-10-11-12 months)

Study Sites (1)

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