Healthy Adults Clinical Trial
Official title:
Investigating Accelerated Learning in Healthy Subjects
Verified date | April 2021 |
Source | The University of Texas at Dallas |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to investigate whether it is possible to accelerate learning and improve associative memory performance in healthy subjects, by (1) applying transcranial Direct Current Stimulation (tDCS) during a verbal paired-associate learning task and by (2) optimizing the learning method with repeated retrieval practice.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 22, 2021 |
Est. primary completion date | April 22, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 35 Years |
Eligibility | Inclusion Criteria: - Age: 18-35 years - Native English Speaker Exclusion Criteria: - History of severe head injuries,epileptic insults, or heart disease - Severe psychiatric disorders and severe untreated medical problems. - Acquainted with the foreign language used in the learning task - Contraindications for tDCS (pregnant women, implanted devices) |
Country | Name | City | State |
---|---|---|---|
United States | The University of Texas of Dallas | Richardson | Texas |
Lead Sponsor | Collaborator |
---|---|
The University of Texas at Dallas |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Associative Memory assessed by a Verbal Paired-Associate memory test | Changes in performance in the Verbal Paired-Associate memory task is compared between the 4 groups (1. tDCS+verbal paired-associate learning task with repeated retrieval practice, 2. tDCS + verbal paired-associate learning task without repeated retrieval practice, 3. Sham tDCS+verbal paired-associate learning task with repeated retrieval practice, 4. Sham tDCS + verbal paired-associate learning task without repeated retrieval practice) to investigate the influence of tDCS and learning method on Associative Memory | baseline and 1 week after the tDCS |
Status | Clinical Trial | Phase | |
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