Board Game Project for Adolescents With Tourette Syndrome

Sponsor
National Taipei University of Nursing and Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05566236
Collaborator
Ministry of Science and Technology, Taiwan (Other), Chang Gung Children's Hospital (Other)
100
1
2
24
4.2

Study Details

Study Description

Brief Summary

The purpose of this research is to investigate the effectiveness of using an evidence-based board game scheme to improve the tics and interpersonal interactions of adolescents with Tourette syndrome.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: board game
N/A

Detailed Description

This study utilizes a randomized control study design. According to the situated learning theory and qualitative research findings, this study develops a board game scheme. This study enrolled adolescents with Tourette syndrome the age of 12 to 20 and their parents as the subjects. The implementation process of this study is to implement a board game workshop once for the experimental group so as to make sure that the subjects understood the rules of a board game. The subjects played the board game at least once at home every week. The 60 minutes parent-child co-learning board game was played for 4 consecutive weeks. On the contrary, the control group continued to receive health education instructions at the outpatient clinic. The research team employs both qualitative and quantitative methods to evaluate the effectiveness and experiences after the subjects underwent the learning scheme. The quantitative effectiveness indicators include self-reported severity of tics of adolescents, depression, positive mental health, and social adjustment. Moreover, this study performed qualitative interviews with parents to understand their parent-child interactive experiences after playing the board game. The researcher believes that this study can help improve the tics of adolescents with Tourette syndrome, as well as enhance their interpersonal interactions and relationships.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Study on the Effectiveness of an Evidence-based Board Game Project to Help Improve Tics and Interpersonal Interactions of Adolescents With Tourette Syndrome: Mixed Methods Research
Actual Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Sep 1, 2024
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

The participants played the board game at least once at home every week. In addition, the 60 minutes parent-child co-learning board game was played for 4 consecutive weeks.

Behavioral: board game
A board game was designed based on situated learning theory and the results of relevant studies. This board game contains a summary, answer booklet, and multiple card game tasks including situations of interpersonal interaction. The participants must discuss, share personal experiences, and find the answer together.
Other Names:
  • Non
  • No Intervention: Control group

    The control group continued to receive health education instructions at the outpatient clinic.

    Outcome Measures

    Primary Outcome Measures

    1. Yale Global Tic Severity Scale [Change from baseline tic severity at 1 month and 3 months]

      The Yale Global Tic Severity Scale will used in this research to evaluate adolescents' tic severity. The Yale Global Tic Severity Scale has a total score ranging from 0 to 100, with the high score indicating a higher tics severity.

    Secondary Outcome Measures

    1. Chinese Version Beck Youth Inventories (subscale-depression) [Change from baseline degree of depression at 1 month and 3 months]

      The Chinese Version Beck Youth Inventories (subscale-depression) will used in this research to evaluate adolescents' depression. The Chinese Version Beck Youth Inventories (subscale-depression) has a total score ranging from 20 to 80, with the high score indicating a higher depression.

    2. Social adjustment scale for adolescents with Tourette syndrome [Change from baseline degree of social adjustment at 1 month and 3 months.]

      The Social adjustment scale for adolescents with Tourette Syndrome will used in this study to evaluate adolescents' degree of self-adjustment in social interactions. The lowest and highest total scores were 17 and 68, respectively. A high score indicates favorable social adjustment.

    3. Positive Mental Health Scale [Change from baseline degree of positive mental health at 1 month and 3 months]

      TThe Positive Mental Health Scale will used in this study to evaluate adolescents' degree of positive mental health. The lowest and highest total scores were 25 and 125, respectively. A high score indicates favorable positive mental health.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years to 20 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. adolescents between the ages of 12 and 20 years were diagnosed with Tourette Syndrome by a pediatrician according to the DSM IV.

    2. ability to speak and understand Mandarin.

    3. adolescents and their parents were willing to participate and fill in consent forms.

    Exclusion Criteria:

    (1) Adolescents with Tourette Syndrome have mental illness and serious diseases.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Chang Gung hospital Taoyuan City Taiwan 333

    Sponsors and Collaborators

    • National Taipei University of Nursing and Health Sciences
    • Ministry of Science and Technology, Taiwan
    • Chang Gung Children's Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Mei-Yin Lee, Associate Professor, National Taipei University of Nursing and Health Sciences
    ClinicalTrials.gov Identifier:
    NCT05566236
    Other Study ID Numbers:
    • 201801998B0C501
    First Posted:
    Oct 4, 2022
    Last Update Posted:
    Oct 4, 2022
    Last Verified:
    Sep 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Mei-Yin Lee, Associate Professor, National Taipei University of Nursing and Health Sciences
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 4, 2022