- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01544699
Impact of Non-invasive Brain Stimulation on Motor Recuperation
January 9, 2024 updated by: Pr Yves Vandermeeren, MD, PhD, University Hospital of Mont-Godinne
tDCS (transcranial direct current stimulation) will be used in chronic stroke patients to improve a variety of functions with superior or inferior limb.
Study Overview
Detailed 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.
Study Type
Interventional
Enrollment (Estimated)
200
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Namur,
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Yvoir,, Namur,, Belgium
- Department of Neurology, CHU Mont-Godinne
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Real stimulation
real tDCS (well, that's the way it is I am not gonna change it)
|
tdcs (ELDITH, Neuroconn, Ilmenau, Germany) transcranial direct current stimulation
|
|
Sham Comparator: Sham
sham tDCS
|
tdcs (ELDITH, Neuroconn, Ilmenau, Germany) transcranial direct current stimulation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change in motor function before/after tDCS
Time Frame: 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
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2012
Primary Completion (Estimated)
December 1, 2025
Study Completion (Estimated)
January 1, 2030
Study Registration Dates
First Submitted
February 10, 2012
First Submitted That Met QC Criteria
March 5, 2012
First Posted (Estimated)
March 6, 2012
Study Record Updates
Last Update Posted (Actual)
January 10, 2024
Last Update Submitted That Met QC Criteria
January 9, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- B039201212957(2)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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