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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05962385
Other study ID # PSYCH-2023-32060
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date August 24, 2023
Est. completion date July 10, 2024

Study information

Verified date August 2023
Source University of Minnesota
Contact Aaron Mclnnes, PhD
Phone 612-300-7801
Email mcinn125@umn.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study will examine whether the benefits of brain stimulation on mental functioning can be enhanced if an individual is actively engaging the target brain networks while receiving brain stimulation. The study includes two separate sessions and people will complete either a cognitive task or a perceptual task while receiving transcranial magnetic stimulation. The study will measure change in brain function with EEG.


Recruitment information / eligibility

Status Recruiting
Enrollment 25
Est. completion date July 10, 2024
Est. primary completion date March 24, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Age 18 - 65, - healthy controls Exclusion Criteria: - Diagnosed psychiatric disorder - Potential contraindications to EEG (e.g. visible scalp abrasions, non-removable hair extensions and/or hair styling that would impede proper EEG recording) - Potential contraindication to TMS (as identified by the TMS safety screener) - Any previous adverse reaction to TMS or MRI - Diagnosed epilepsy or previously experienced a seizure - Diagnosed neurological condition, such as stroke or tinnitus - Experienced a head trauma that was diagnosed as concussion - Current use of, or recent withdrawal from, medications that can increase the risk of seizure - Currently pregnant - Any metal in the head (excluding mouth) - Any implanted medical device

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Brain state while receiving TMS
Brain state whilst receiving TMS - cognitive control or perceptual. Repeated measures design, so all participants receive the same procedures.

Locations

Country Name City State
United States University of Minnesota Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Theta-gamma cross frequency coupling A metric of brain function measured with EEG - the coupling of theta oscillation phase with gamma power. This will be measured immediately following the intervention (TMS stimulation). 0-500 ms after each TMS stimulus
Primary Cortical excitability TMS-evoked potentials will be measured with EEG to examine cortical excitability after TMS. This will be measured immediately following the intervention (TMS stimulation). 60-300 ms after each TMS stimulus
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