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Effects of PrTMS on Performance

NCT05353244 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2024-01-17

No results posted yet for this study

Summary

The purpose of this study is to assess the ability of a form of non-invasive brain stimulation called personalized repetitive transcranial magnetic stimulation, or PrTMS, to enhance cognitive performance and sleep quality from baseline metrics.

Conditions

  • Sleep Quality
  • Cognition Improvement

Interventions

DEVICE

PrTMS

Each participant will receive a personalized rTMS treatment based on their individual alpha frequency.

DEVICE

Sham

Using a sham coil that looks and sounds like an actual TMS coil, each participant will receive sham rTMS treatments.

Sponsors & Collaborators

  • West Virginia University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
42 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-12-04
Primary Completion
2023-12-04
Completion
2023-12-04
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05353244 on ClinicalTrials.gov