RECRUITING

Brain Stimulation Effects on Cognitive Task Performance

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 purpose of this study is to determine optimal task design parameters for the measurement of transcranial magnetic stimulation (TMS) effects on cognition.

Official Title

Brain Stimulation Effects on Cognitive Task Performance

Quick Facts

Study Start:2023-04-20
Study Completion:2025-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05556655

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. * Right-handed
  2. * Fluent in English
  1. * History of seizures or epilepsy
  2. * Family history of epilepsy
  3. * Significant medical or neurological diagnoses
  4. * History of common headache or migraine
  5. * History of common or recent syncope
  6. * History of moderate/severe, multiple mild, or past 12 months head injury
  7. * History of psychiatric, psychological, or neurodevelopmental disorder
  8. * History of alcohol or recreational drug abuse or dependence
  9. * Current visual or hearing difficulties that interfere with cognitive testing
  10. * History of cochlear implants
  11. * Current pregnancy
  12. * History of metal in the head or neck (except braces and fillings)
  13. * Current non-removable piercings in the neck or head
  14. * History of implanted neurostimulator
  15. * History of cardiac pacemaker or intracardiac lines
  16. * History of medication infusion device
  17. * Current use of medications that increase the excitability of the brain
  18. * History of problems with TMS or MRI procedures
  19. * History of EEG for suspected epilepsy
  20. * Alcohol or recreational drug use in the 48 hours prior to TMS
  21. * Inadequate sleep in the 48 hours prior to TMS
  22. * Headache or feeling faint in the 24 hours prior to TMS.

Contacts and Locations

Study Contact

Michael Thomas, PhD
CONTACT
(970) 491-6820
Michael.L.Thomas@colostate.edu

Study Locations (Sites)

Colorado State University Department of Psychology
Fort Collins, Colorado, 80523
United States

Collaborators and Investigators

Sponsor: Colorado State University

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 Date2023-04-20
Study Completion Date2025-01-01

Study Record Updates

Study Start Date2023-04-20
Study Completion Date2025-01-01

Terms related to this study

Keywords Provided by Researchers

  • Transcranial Magnetic Stimulation
  • TMS

Additional Relevant MeSH Terms

  • Cognitive Function