A Trial of Two-Week Brain Stimulation for Teenagers With ADHD

Description

The objective of this clinical trial is to examine whether non-invasive brain stimulation can modulate dysfunctional brain dynamics underlying adolescent ADHD to subsequently improve clinical symptoms.

Conditions

ADHD

Study Overview

Study Details

Study overview

The objective of this clinical trial is to examine whether non-invasive brain stimulation can modulate dysfunctional brain dynamics underlying adolescent ADHD to subsequently improve clinical symptoms.

A Trial of Two-Week Brain Stimulation for Teenagers With ADHD

A Trial of Two-Week Brain Stimulation for Teenagers With ADHD

Condition
ADHD
Intervention / Treatment

-

Contacts and Locations

East Providence

E. P. Bradley Hospital, East Providence, Rhode Island, United States, 02915

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Ability to provide assent and have parent provide parental permission
  • 2. English fluency of the participant and the legal guardian/parent
  • 3. 12-18 years
  • 4. Parent rating on BRIEF-2 Working Memory: Greater than 1.0 SD above normative mean.
  • 5. IQ \> 80
  • 6. Clinical diagnosis of attention deficit hyperactivity disorder (ADHD): predominantly inattentive type, predominantly hyperactive/impulsive type, combined type, or unspecified type. Diagnostic criteria will be confirmed with NICHQ Vanderbilt Assessment Scales-Parent.
  • 7. Participants are allowed to continue clinical ADHD treatments. However, changes to ADHD treatments cannot be made during the entirety of study participation. Confirming a plan of treatment stability will occur as part of initial inclusion criteria. We will check on treatment stability at the start of each two-week phase with the participant and parent, and document accordingly. Changes to treatment will be reviewed by a physician and may result in study termination.
  • 1. Intracranial pathology from a known genetic disorder (e.g., NF1, tuberous sclerosis) or from acquired neurologic disease (e.g. stroke, tumor), cerebral palsy, history of severe head injury, or significant dysmorphology
  • 2. History of fainting spells of unknown or undetermined etiology that might constitute seizures
  • 3. History of seizures, diagnosis of epilepsy, or immediate (1st degree relative) family history epilepsy
  • 4. Any progressive (e.g., neurodegenerative) neurological disorder
  • 5. Chronic (particularly) uncontrolled medical conditions that may cause a medical emergency in case of a provoked seizure (cardiac malformation, cardiac dysrhythmia, asthma, etc.)
  • 6. Contraindicated metal implants in the head, brain or spinal cord (excluding dental implants, braces or fillings)
  • 7. Non-removable makeup or piercings
  • 8. Pacemaker
  • 9. Implanted medication pump
  • 10. Vagal nerve stimulator
  • 11. Deep brain stimulator
  • 12. TENS unit (unless removed completely for the study)
  • 13. Ventriculo-peritoneal shunt
  • 14. Signs of increased intracranial pressure
  • 15. Intracranial lesion (including incidental finding on MRI)
  • 16. History of head injury resulting in prolonged loss of consciousness
  • 17. Substance abuse or dependence within past six months (i.e., DSM-5 substance use disorder criteria)
  • 18. Chronic treatment with prescription medications that decrease cortical seizure threshold, not including psychostimulant medication if deemed to be medically safe as part of the medical review process.
  • 19. Active psychosis or mania
  • 20. Current suicidal intent
  • 21. Current pregnancy
  • 22. Significant visual, hearing or speech impairment
  • 23. Current wards of the state

Ages Eligible for Study

12 Years to 18 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Bradley Hospital,

Study Record Dates

2025-10-01