COMPLETED

State Dependence of Prefrontal Transcranial Magnetic Stimulation

Conditions

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 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.

Official Title

State Dependence of Prefrontal Transcranial Magnetic Stimulation

Quick Facts

Study Start:2023-08-24
Study Completion:2025-11-17
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05962385

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 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age 18 - 65,
  2. * healthy controls
  1. * Diagnosed psychiatric disorder
  2. * Potential contraindications to EEG (e.g. visible scalp abrasions, non-removable hair extensions and/or hair styling that would impede proper EEG recording)
  3. * Potential contraindication to TMS (as identified by the TMS safety screener)
  4. * Any previous adverse reaction to TMS or MRI
  5. * Diagnosed epilepsy or previously experienced a seizure
  6. * Diagnosed neurological condition, such as stroke or tinnitus
  7. * Experienced a head trauma that was diagnosed as concussion
  8. * Current use of, or recent withdrawal from, medications that can increase the risk of seizure
  9. * Currently pregnant
  10. * Any metal in the head (excluding mouth)
  11. * Any implanted medical device

Contacts and Locations

Principal Investigator

Alik Widge
PRINCIPAL_INVESTIGATOR
University of Minnesota

Study Locations (Sites)

University of Minnesota
Minneapolis, Minnesota, 55455
United States

Collaborators and Investigators

Sponsor: University of Minnesota

  • Alik Widge, PRINCIPAL_INVESTIGATOR, University of Minnesota

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 Date2023-08-24
Study Completion Date2025-11-17

Study Record Updates

Study Start Date2023-08-24
Study Completion Date2025-11-17

Terms related to this study

Additional Relevant MeSH Terms

  • Healthy