Neurofeedback From the Supplementary Motor Area for Tourette Syndrome

Description

This is a clinical trial where adolescents aged 10-16 years old with Tourette Syndrome (or chronic tic disorder) are randomized to receive either real-time functional magnetic resonance imaging (fMRI) neurofeedback targeting the supplementary motor area (for the experimental intervention) or real-time fMRI neurofeedback (NF) from a control region (for the control intervention).

Conditions

Tourette Syndrome in Adolescence

Study Overview

Study Details

Study overview

This is a clinical trial where adolescents aged 10-16 years old with Tourette Syndrome (or chronic tic disorder) are randomized to receive either real-time functional magnetic resonance imaging (fMRI) neurofeedback targeting the supplementary motor area (for the experimental intervention) or real-time fMRI neurofeedback (NF) from a control region (for the control intervention).

Neurofeedback From the Supplementary Motor Area for Tourette Syndrome

Neurofeedback From the Supplementary Motor Area for Tourette Syndrome

Condition
Tourette Syndrome in Adolescence
Intervention / Treatment

-

Contacts and Locations

New Haven

Yale University School of Medicine, New Haven, Connecticut, United States, 06520

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

  • * Boys and girls, 10 to 16 years of age
  • * A current diagnosis of Tourette Syndrome (TS) or chronic tic disorder (CTD), with active tics that can be executed without head movement, and a YGTSS score of at least 13 (for TS participants) or at least 12 (for CTD participants)
  • * Currently stable medication treatment and no planned changes in medication for the duration of the study.
  • * Family residence within 2 hours of Yale Medical Center with ability and willingness to attend assessment and fMRI visits.
  • * Children and their parents are expected to be able to speak and understand spoken English in order to participate in a clinical assessment of TS and related psychopathology.
  • * Subjects will be free of: 1) metal medical implants or braces, 2) pregnancy, and will have 3) a body weight of less than 250 lbs. and 4) no claustrophobia.
  • * Intelligence quotient below 80
  • * Current diagnosis of autism spectrum disorder, bipolar or psychotic disorder or current suicidality
  • * Significant medical condition such as heart disease, hypertension, liver or renal failure, pulmonary disease, seizure disorder
  • * Recently initiated psychotherapy. Participation in the study will not be allowed within 8 weeks of the initiation of psychotherapy. Ongoing, concurrent psychotherapy (that was initiated at least 8 weeks previously) for the child will be allowed, but parents will be asked not to initiate any new psychotherapy for the child during the study
  • * Subjects may also be excluded after the first MR scan if we are unable to localize the two regions in their brain that are used as targets for the active and control neurofeedback conditions.

Ages Eligible for Study

10 Years to 16 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Yale University,

Michelle Hampson, PhD, PRINCIPAL_INVESTIGATOR, Yale University

Study Record Dates

2027-01-20