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Neurofeedback for Tourette Syndrome

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Yale University

Status

Completed

Conditions

Chronic Tic Disorder
Tourette Syndrome

Treatments

Procedure: Sham feedback
Procedure: Neurofeedback

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01702077
R01MH095789 (U.S. NIH Grant/Contract)
0206017435

Details and patient eligibility

About

The aim of this study is to train patients with tic disorders to control activity in a region of their brain that has been associated with the urge to tic. Patients will be given direct feedback regarding activity in this brain area while they are undergoing functional magnetic resonance imaging (fMRI) scanning, and will try to learn to control activity in the region during these feedback sessions. In separate sessions, patients will be given sham feedback based on the brain patterns of a prior subject rather than their own brain patterns. Our primary hypothesis is that the biofeedback training will reduce their tic symptoms more than the sham feedback.

Enrollment

21 patients

Sex

All

Ages

11 to 19 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of Tourette Syndrome or Chronic Tic Disorder
  • currently active tics
  • aged 11-19
  • ability to execute most common tics without moving head while lying on back

Exclusion criteria

  • Blindness (because feedback is provided visually)
  • Lifetime diagnosis of pervasive developmental disorder, bipolar disorder, or psychotic disorder.
  • Presence of any serious psychiatric or psychosocial condition requiring initiation of new treatment or change in current treatment.
  • Neurological conditions affecting central nervous system, with the exception that predisposition to migraine will not be grounds for exclusion
  • Change in medication in the month prior to beginning the study
  • Unwillingness to keep medication stable over the course of the intervention
  • Full braces (but some retainers are OK)
  • Claustrophobia of a degree that they cannot comfortably be scanned
  • If common tics involve dramatic changes in breathing that could alter blood oxygenation measurements
  • Inability to keep head still while executing most common tics
  • Inability to keep head still in mock scanner
  • Inability or unwillingness to understand or follow the instructions
  • Pregnancy or possible pregnancy
  • Subjects may also be excluded after the first magnetic resonance scan if we are unable to localize a region of their supplementary motor area involved in tics - leaving us without a target area for biofeedback.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

21 participants in 2 patient groups

Neurofeedback first
Experimental group
Description:
Neurofeedback then sham feedback
Treatment:
Procedure: Neurofeedback
Procedure: Sham feedback
Sham first
Experimental group
Description:
Sham feedback then neurofeedback
Treatment:
Procedure: Neurofeedback
Procedure: Sham feedback

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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