Investigating HD-tDCS in Improving Word Finding and Memory Retrieval in Individuals With MCI
NCT ID: NCT03446508
Last Updated: 2022-02-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
NA
INTERVENTIONAL
2017-11-18
2022-01-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
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Active frontal
Active HD-tDCS
Active frontal
1\) active HD-tDCS will be administered
Active parietal
Active HD-tDCS
Active parietal
2\) active HD-tDCS will be administered
Sham control
Sham HD-tDCS
Sham
3\) sham HD-tDCS - no current
Interventions
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Active frontal
1\) active HD-tDCS will be administered
Active parietal
2\) active HD-tDCS will be administered
Sham
3\) sham HD-tDCS - no current
Eligibility Criteria
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Inclusion Criteria
2. Capable of understanding and signing an informed consent
3. Experiencing severe memory problems
Exclusion Criteria
2. Pace maker / defibrillator
3. Pregnancy
40 Years
90 Years
ALL
No
Sponsors
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The University of Texas at Dallas
OTHER
Responsible Party
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Sven Vanneste
Associate professor
Principal Investigators
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Sven Vanneste, PhD
Role: PRINCIPAL_INVESTIGATOR
The University of Texas at Dallas
Locations
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University of Texas at Dallas
Richardson, Texas, United States
Countries
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Other Identifiers
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18-21
Identifier Type: -
Identifier Source: org_study_id
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