- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05492435
CEEG Changes After Tdcs and Dual-task Training
Changes in EEG Microestates After Combined Treatment od Tdcs and Dual-task Training in Stroke Patients: a Cross-roads, Sham-controlled,Double-blind Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: LETICIA MARIA
- Phone Number: 81 993684588
- Email: leticiamaria.fisio@gmail.com
Study Locations
-
-
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João Pessoa, Brazil
- Recruiting
- Aging and Neuroscience Studies Laboratory
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Contact:
- Suellen Andrade
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Individuals diagnosed with stroke for more than 6 months;
Proven by means of magnetic resonance imaging or computed tomography;
Individuals aged 18 and over;
Both sexes;
Patients with mild to moderate degree of injury severity (NIHHS < 17 points)
Exclusion Criteria:
- Individuals who are unable to communicate verbally;
Use of drugs that modulate the activity of the Central Nervous System;
Carriers of implanted metallic or electronic devices; cardiac pacemaker;
Habitual use of drugs or alcohol;
Report of history of epilepsy; gestation; people with traumatic brain injury or tumors.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: m1 stimulation + dual task training
participants will receive real current over the primary motor area (M1)
|
tDCS can regulate cortical excitability by influencing membrane polarity, where anodic current increases excitability and cathodic current reduces excitability.
Therefore, in post-stroke patients when the anode is applied to the cerebral hemisphere ipsilesional to the lesion or the cathode to the contralesional hemisphere, the balance between the interhemispheres tends to be restored.
|
|
Experimental: stimulation in M1 and DLPF + dual task training
participants will receive real current over the M1 and over the dorsolateral prefrontal area (DLPFC)
|
tDCS can regulate cortical excitability by influencing membrane polarity, where anodic current increases excitability and cathodic current reduces excitability.
Therefore, in post-stroke patients when the anode is applied to the cerebral hemisphere ipsilesional to the lesion or the cathode to the contralesional hemisphere, the balance between the interhemispheres tends to be restored.
|
|
Sham Comparator: sham stimulation + dual task training
Participants will receive simulated stimulation
|
tDCS can regulate cortical excitability by influencing membrane polarity, where anodic current increases excitability and cathodic current reduces excitability.
Therefore, in post-stroke patients when the anode is applied to the cerebral hemisphere ipsilesional to the lesion or the cathode to the contralesional hemisphere, the balance between the interhemispheres tends to be restored.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in EEG microstates in each stimulation condition
Time Frame: immediately after the sessions
|
Microstate analysis was performed using the EEGLAB microstate plugin developed by Thomas Koenig (Koenig, 2021).
First, at the individual level, we compute global field power (GFP) across all channels and microstate segmentation using the modified k-means clustering algorithm method to isolate map topographies.
Polarity was ignored during microstate analysis.
After obtaining the microstate segmentation of each participant, we calculated an average of the microstate segmentation of each group as models.
The successive original individual EEG series were then divided into four classic microstate maps (they are labeled as four classes A, B, C and D, which are left-right direction (type A), left-right direction (type B), anteroposterior direction (type C) and frontocentral maximum (type D)).
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immediately after the sessions
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cognitive function - trail test (TMT) A and B
Time Frame: immediately after the sessions
|
TMT consists of connecting letters in the order they appear in the alphabet (A tracks); or letters to numbers, also following the sequence in which they appear in the alphabet, for example, 1-A-2-B and so on (B tracks), with the possibility of evaluating the cognitive components of planning, organization, attention, perseverance and memory.
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immediately after the sessions
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Cognitive function - clock drawing test
Time Frame: immediately after the sessions
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Currently, the RDT is widely used, it is simple to apply and quick to perform, which assesses several cognitive dimensions, such as memory, motor function, executive function and verbal comprehension.
Regarding its score, the Shulman scale scores 5 points in total and a cut-off point equal to 3. The Mendez scale scores up to 20 points for the perfect design of the watch, with a cut-off point equal to 18 points.
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immediately after the sessions
|
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Cognitive function - verbal fluency test (VF).
Time Frame: immediately after the sessions
|
The VF test assesses several domains such as working memory, language, organizational skills and sequencing.
In this test, the patient is asked to speak the largest number of words (within each required category).
In the VF test, responses are scored, but repetitions are not considered.
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immediately after the sessions
|
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motor function
Time Frame: immediately after the sessions
|
The Timed Up and Go Test (TUG) test will be used
|
immediately after the sessions
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Suellen Andrade, Dra, Federal University of Paraíba
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- microstates_stroke
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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