RECRUITING

Cognitive Enhancement Through Model-based and Individualized Neurostimulation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to learn about the effects of transcranial electric stimulation on attentional control and brain dynamics in healthy adults. The main questions are: Does stimulation affect how subjects exert attentional control? Do mathematical models predict brain activity changes in response to stimulation? Participants will have electroencephalography (EEG) brain data recorded while: They sit relaxed They receive stimulation, while relaxed They receive stimulation while completing computerized tasks to measure cognitive abilities ("cognitive tasks") They receive sham (ineffective) stimulation during cognitive tasks

Official Title

Cognitive Enhancement Through Model-based and Individualized Neurostimulation

Quick Facts

Study Start:2024-02-13
Study Completion:2024-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06235970

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Healthy younger adults (ages 18 to 45). Community-living men, women or non-binary, aged 18-45
  1. * Taking psychotropic medication or medication with cognitive side effects
  2. * Medical disorder that affects cognitive or motor function
  3. * Past/present head injury associated with loss of consciousness or neurological sequelae
  4. * Prior occurrence of seizure of any origin
  5. * Skin conditions affecting the scalp
  6. * Scalp tattoos
  7. * Rashes, sores or open wounds on scalp or face

Contacts and Locations

Study Contact

Todd Braver, PhD
CONTACT
3149354153
tbraver@wustl.edu
Carol Cox
CONTACT
3147152714
ccox@wustl.edu

Study Locations (Sites)

Washington University
Saint Louis, Missouri, 63130
United States

Collaborators and Investigators

Sponsor: Washington University School of Medicine

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-13
Study Completion Date2024-12-31

Study Record Updates

Study Start Date2024-02-13
Study Completion Date2024-12-31

Terms related to this study

Keywords Provided by Researchers

  • tES, EEG

Additional Relevant MeSH Terms

  • Transcranial Electrical Stimulation (tES)