Actively Recruiting

Phase Not Applicable
Age: 14Years - 21Years
All Genders
ID06873841

Can the Cognitive-Psychophysiological Treatment of Tics be Optimized Through Biofeedback in Adolescents and Emerging Adults With Tourette Syndrome? - A Randomized Clinical Trial

Led by Université du Québec a Montréal · Updated on 2025-07-08

150

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

Université du Québec a Montréal

Lead Sponsor

C

Ciusss de L'Est de l'Île de Montréal

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the effectiveness of a cognitive-psychophysiological (CoPs) therapy with or without biofeedback in treating tics in young people aged 14 to 21 with Tourette Syndrome. This study aims to determine if adding biofeedback to the CoPs therapy improves tic severity and overall clinical impressions more than CoPs therapy alone. The study also explores how psychosocial, neurocognitive, and biological factors may predict treatment improvements. Participants will undergo a pre-test phase involving two interviews lasting three hours each, assessing tic severity and related psychosocial, biological, and neurocognitive functions. Following this, participants will attend 10 to 12 weekly therapy sessions. One group will receive CoPs therapy alone, which includes six therapeutic steps such as awareness training and relapse prevention. Another group will receive the same CoPs therapy plus 25 minutes of electromyographic biofeedback exercises designed to help control muscle activity. Adolescents aged 14 to 17 receive a tailored treatment guide to support their understanding. Throughout the study, participants will be evaluated using multiple tests before treatment, immediately after, and at 3- and 6-month follow-ups. These tests measure tic severity, stress, depression, self-esteem, quality of life, and various cognitive functions. The main outcome is monitored by the Yale Global Tic Severity Scale (YGTSS) over about one year. This thorough assessment helps researchers understand the therapy's impact and track any changes in tic symptoms and related areas.

CONDITIONS

Brief Title

Cognitive-psychophysiological Treatment for Tics in Young People With Tourette's Syndrome With or Without Biofeedback

Who Can Participate

Age: 14Years - 21Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a diagnosis of Tourette Syndrome or experience bothersome tics
  • Be aged 14 to 21 years inclusive at the start of therapy
Not Eligible

You will not qualify if you...

  • Present a sensorimotor impairment
  • Have a diagnosis of intellectual disability with an IQ below 75
  • Alcohol or drug abuse
  • Have a neurological issue such as hemifacial spasms or Huntington's disease
  • Changed medication one month or less before therapy start and up to last measurement without informing research team
  • Receiving another treatment for tics simultaneously without informing research team

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - Up to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 10 to 12 weeks

Participants receive cognitive-psychophysiological therapy with or without biofeedback exercises, involving weekly sessions focused on tic management and behavioral restructuring.

Weekly visits for 10 to 12 weeks

Follow-up

Duration - 6 months after treatment completion

Participants are monitored through repeated assessments to evaluate the effects of treatment over time.

3 visits (at 3 months and 6 months post-treatment, plus post-treatment assessment)

Trial Site Locations

Total: 1 location

1

Centre intégré universitaire de santé et de services sociaux du Nord-de-l'Île-de-Montréal, Hôpital Rivières-des-Prairies

Montreal, Quebec, Canada, H1E 1A4

Actively Recruiting

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Research Team

J

Julie Leclerc, Psychology

A

Audrey-Ann Lachance

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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