RECRUITING

Exploring Neurophysiological Markers of Brain Health

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Conditions

Healthy LifestyleHealth-Related Behavior

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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 combination of transcranial magnetic stimulation (TMS) and electroencephalography (EEG) has been suggested as a promising brain imaging tool for identifying biomarkers of brain health. In this pilot study, study investigators will explore the neurophysiological metrics of brain health with a non-invasive brain imaging technique, alongside behavioral and fMRI metrics collected through another study (NCT04869111).

Official Title

Exploring Markers of Brain Health With EEG and TMS: A Pilot Study

Quick Facts

Study Start:2025-05-01
Study Completion:2027-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06731452

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:22 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Must be an active brain imaging participant in The BrainHealth Project (NCT04869111)
  2. * Minimum age of 22
  3. * Fluent in English
  4. * Able to read \& hear information over a computer
  5. * Must pass an MRI safety screener to assess the presence of contraindicators for MRI compatibility (i.e., non-removable metal within/on the body, claustrophobia, pregnancy, non-correctable vision problems, head trauma, and CNS disease)or other standard requirements as determined by the Imaging Center.
  6. * Must pass a modified TMS Adult Safety Screen
  7. * Meet all criteria for study as determined by the study physician
  1. * A diagnosis of a neurodegenerative disease
  2. * A history of stroke, concussion, or brain injury that currently hinders them from functioning at their prior level
  3. * A diagnosis of autism spectrum disorder that currently hinders them from functioning independently.
  4. * Metallic brain implants or fragments (like a shunt, pacemaker, clips, coils, bullet fragments, cochlear implants)
  5. * Magnetically activated implants or electronically implanted devices
  6. * Medication pumps
  7. * Personal or family history of epilepsy, seizure(s), seizure disorder.
  8. * History of, or risk factors for syncope (fainting)
  9. * Report significant cognitive challenges
  10. * Report untreated health issues (like substance abuse, hypertension, hypo- or hyper-thyroidism)
  11. * Have claustrophobia

Contacts and Locations

Study Contact

Erin Venza, MS
CONTACT
972-883-3208
erin.venza@utdallas.edu

Principal Investigator

Sandra Chapman, PhD
PRINCIPAL_INVESTIGATOR
University of Texas at Dallas

Study Locations (Sites)

Center for BrainHealth at The University of Texas at Dallas
Dallas, Texas, 75235
United States

Collaborators and Investigators

Sponsor: The University of Texas at Dallas

  • Sandra Chapman, PhD, PRINCIPAL_INVESTIGATOR, University of Texas at Dallas

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 Date2025-05-01
Study Completion Date2027-05-31

Study Record Updates

Study Start Date2025-05-01
Study Completion Date2027-05-31

Terms related to this study

Additional Relevant MeSH Terms

  • Healthy Lifestyle
  • Health-Related Behavior