Online Mindfulness-based Tic Reduction (Phase Two)

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Brief Title

Online Mindfulness-based Tic Reduction (Phase Two)

Official Title

Online Mindfulness-based Tic Reduction: Development and Testing (Phase Two)

Brief Summary

      Tourette Syndrome (TS) and Persistent Tic Disorder (PTD) are chronic and potentially
      disabling neurobiological conditions. Although a range of pharmacological and psychosocial
      treatments exists, a significant number of individuals either do not respond to the current
      treatments or find them unacceptable. Thus, it is essential that researchers continue to
      develop and test novel treatment approaches.

      In this randomized controlled trial the investigators will compare two different online
      group-based interventions for tics: a mindfulness-based program (Mindfulness-based
      Intervention for Tics (MBIT), and a psychoeducational and supportive therapy program (Tic
      Information and Coping Strategies (TICS)). The purpose of this study is to determine which
      intervention is more helpful for adults with a tic disorder.

Study Type

Interventional

Primary Outcome

Change in Yale Global Tic Severity Scale (YGTSS) Total Tic Severity Score

Secondary Outcome

 Clinical Global Impressions Scale

Condition

Tourette Syndrome

Intervention

Mindfulness-based Intervention for Tics

Study Arms / Comparison Groups

 Mindfulness-based Intervention for Tics
Description:  8-week group-based mindfulness-based program

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status

Behavioral

Estimated Enrollment

37

Start Date

November 9, 2018

Completion Date

December 2, 2020

Primary Completion Date

December 2, 2020

Eligibility Criteria

        Inclusion Criteria:

          1. be 18 years of age or older,

          2. possess a primary diagnosis of Tourette Syndrome or Persistent Tic Disorder,

          3. be fluent in English

          4. reside in the United States,

          5. either not be taking any tic suppressant medication or other psychotropic medication
             or be at a stable dose for 8 weeks prior to the baseline assessment and throughout the
             study

        Exclusion Criteria:

          1. be receiving concurrent psychotherapy for the duration of the study

          2. have prior extensive experience with mindfulness and/or meditation and

          3. have another medical or psychological condition that would prevent the individual from
             fully engaging in the study or require a higher level of care (e.g., suicidality).

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Hannah Reese, Ph.D., ,

Location Countries

United States

Location Countries

United States

Administrative Informations

NCT ID

NCT03771235

Organization ID

2018-30

Responsible Party

Principal Investigator

Study Sponsor

Bowdoin College

Collaborators

 Massachusetts General Hospital

Study Sponsor

Hannah Reese, Ph.D., Principal Investigator, Assistant Professor

Verification Date

January 2021