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NCT01544699 Clinical Trial

Impact of Non-invasive Brain Stimulation on Motor Recuperation

Stroke Clinical Trial

Official title:
Impact of Non-invasive Brain Stimulation on Motor Recuperation

Clinical Trial Details — Status: Suspended

Administrative data
NCT number NCT01544699
Other study ID # B039201212957(2)
Secondary ID
Status Suspended
Phase N/A
First received
Last updated
Start date January 2012
Est. completion date January 2030

Study information
Verified date January 2024
Source University Hospital of Mont-Godinne
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

tDCS (transcranial direct current stimulation) will be used in chronic stroke patients to improve a variety of functions with superior or inferior limb.

Description:

tDCS will be used in chronic stroke patients to improve a variety of functions such as motor functions with superior or inferior limb. tDCS will be applied in a placebo-controlled, double-blind, randomised fashion. Behavioural data will be collected before and after tDCS, as well as brain functional imaging data.

Recruitment information / eligibility
Status Suspended
Enrollment 200
Est. completion date January 2030
Est. primary completion date December 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - stroke with at least slight deficit in superior or inferior limb Exclusion Criteria: - epilepsy - contraindication to tDCS and/or to fMRI - presence of metal in the head - inability to understand/complete behavioural tasks - chronic intake of alcohol or recreative drugs - major health condition - presence of pacemaker - pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• tDCS (ELDITH)
tdcs (ELDITH, Neuroconn, Ilmenau, Germany) transcranial direct current stimulation

Locations
Country Name City State
Belgium Department of Neurology, CHU Mont-Godinne Yvoir, Namur,

Sponsors (1)
Lead Sponsor Collaborator
University Hospital of Mont-Godinne

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary change in motor function before/after tDCS Motor performance improvement with inferior or superior limb Baseline (>6 months after stroke), immediately after intervention (30min of tDCS), 10-20-30-40-50-60 min after intervention; long-term after intervention : 1-2-3-4 weeks
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