The Impact of a Virtual Magic Trick Training Program

Sponsor
University of Alabama at Birmingham (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05664841
Collaborator
(none)
60
1
2
22.1
2.7

Study Details

Study Description

Brief Summary

The proposed project will attempt to confirm the benefits of a structured magic trick training program (MTTP) experience in adolescents with unilateral cerebral palsy. Benefits of participating in a 6-week virtual MTTP will be evaluated using validated assessments to measure the extent to which adolescents use two hands in activities and improve in social-emotional competencies.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: magic trick training
Phase 2

Detailed Description

The proposed study will employ a RCT to test the two hypotheses. The design of the MTTP is based on the SELframework. The study will incorporate a 2 x 3 two-way factorial design with repeated measures at three time points.The two between-subject factor conditions will be participation in a MTTP versus a waitlist control condition that willbe evaluated at baseline, immediately post-program, and at 6-week follow-up (within-subject factor conditions). Sixty adolescents with UCP will be recruited for this study.

Aim 1. Evaluate the therapeutic benefits of a 6-week virtual MTTP on the extent of two-handed use tocomplete daily activities, social-emotional functioning, and emotional stress among adolescents with UCP.

Hypothesis #1: Adolescents with UCP who participate in a virtual MTTP will demonstrate increased use of two handsto perform daily activities, better social-emotional functioning, and a reduction in emotional stress compared to waitlistcontrols at the conclusion of a 6-week MTTP.

Hypothesis #2: The positive impact of the virtual MTTP on the participants' improved number of activities performedusing two hands, social-emotional functioning, and reduction in emotional stress will be maintained at 6-week follow-up.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized controlled trialRandomized controlled trial
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Impact of a Virtual Magic Trick Training Program on Social Emotional Functioning in Adolescents With Hemiparesis
Anticipated Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Feb 1, 2025
Anticipated Study Completion Date :
Feb 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: magic trick training

Participation in a 6 weekly virtual magic trick training camp with three lessons per week.

Behavioral: magic trick training
A typical session will begin with the magician demonstrating a magic trick then revealing the secret move of the trick.The participants will learn and practice each trick. With assistance from the magician, participants will develop an oralstory presentation for the trick. After participants master one trick, the magician will demonstrate and teach the next.

No Intervention: waitlist control

Participation in usual daily activities.

Outcome Measures

Primary Outcome Measures

  1. Children's HandExperience Questionnaire (CHEQ) [baseline]

    The CHEQ 2.0 evaluates the extent of participants in using their affected hand. Participants are asked to indicate how they normally perform 27 daily activities where two hands are usually required, i.e. did they typically use one hand, use two hands, or with help. Participants respond verbally to each of the 27 activity statements. The number of activities in which the participant used two hands is the outcome.

  2. Children's HandExperience Questionnaire (CHEQ) [at 6 week]

    The CHEQ 2.0 evaluates the extent of participants in using their affected hand. Participants are asked to indicate how they normally perform 27 daily activities where two hands are usually required, i.e. did they typically use one hand, use two hands, or with help. Participants respond verbally to each of the 27 activity statements. The number of activities in which the participant used two hands is the outcome.

  3. Children's HandExperience Questionnaire (CHEQ) [at 12 week]

    The CHEQ 2.0 evaluates the extent of participants in using their affected hand. Participants are asked to indicate how they normally perform 27 daily activities where two hands are usually required, i.e. did they typically use one hand, use two hands, or with help. Participants respond verbally to each of the 27 activity statements. The number of activities in which the participant used two hands is the outcome.

  4. Social Skills Improvement System (SSIS) [baseline]

    The Social Skills scale of the SSIS consists of seven subscales: Communication, Cooperation, Assertion, Responsibility, Empathy, Engagement, and Self-control. The social skills scale has 46 items rated on a 4-point Likert-type scale (0 = not true, 3 = very true) with higher scores representing better social skills.

  5. Social Skills Improvement System (SSIS) [at 6 week]

    The Social Skills scale of the SSIS consists of seven subscales: Communication, Cooperation, Assertion, Responsibility, Empathy, Engagement, and Self-control. The social skills scale has 46 items rated on a 4-point Likert-type scale (0 = not true, 3 = very true) with higher scores representing better social skills.

  6. Social Skills Improvement System (SSIS) [at 12 week]

    The Social Skills scale of the SSIS consists of seven subscales: Communication, Cooperation, Assertion, Responsibility, Empathy, Engagement, and Self-control. The social skills scale has 46 items rated on a 4-point Likert-type scale (0 = not true, 3 = very true) with higher scores representing better social skills.

  7. Strengths and Difficulties Questionnaire (SDQ) [baseline]

    SDQ (peer problem scale and prosocial scale) consists of 10 items rated on a 3-point Likert-type scale (not true=1 to certainly true=3), with higher scores indicating higher psychological problems. Some items require reverse scoring.

  8. Strengths and Difficulties Questionnaire (SDQ) [at 6 week]

    SDQ (peer problem scale and prosocial scale) consists of 10 items rated on a 3-point Likert-type scale (not true=1 to certainly true=3), with higher scores indicating higher psychological problems. Some items require reverse scoring.

  9. Strengths and Difficulties Questionnaire (SDQ) [at 12 week]

    SDQ (peer problem scale and prosocial scale) consists of 10 items rated on a 3-point Likert-type scale (not true=1 to certainly true=3), with higher scores indicating higher psychological problems. Some items require reverse scoring.

  10. Rosenberg Self Esteem Scale (RSES) [baseline]

    RSES consists of 10 items rated on a 4-point Likert-type scale, with higher scores indicate higher self-esteem.

  11. Rosenberg Self Esteem Scale (RSES) [at 6 week]

    RSES consists of 10 items rated on a 4-point Likert-type scale, with higher scores indicate higher self-esteem.

  12. Rosenberg Self Esteem Scale (RSES) [at 12 week]

    RSES consists of 10 items rated on a 4-point Likert-type scale, with higher scores indicate higher self-esteem.

  13. Dimensional Mastery Questionnaire (DMQ) [baseline]

    DMS consists of 41 items rated on a 5-point Likert-type scale (not like me/my child=1 to exactly like me/my child=5) with higher scores representing strong mastery motivation.

  14. Dimensional Mastery Questionnaire (DMQ) [at 6 week]

    DMS consists of 41 items rated on a 5-point Likert-type scale (not like me/my child=1 to exactly like me/my child=5) with higher scores representing strong mastery motivation.

  15. Dimensional Mastery Questionnaire (DMQ) [at 12 week]

    DMS consists of 41 items rated on a 5-point Likert-type scale (not like me/my child=1 to exactly like me/my child=5) with higher scores representing strong mastery motivation.

  16. Self-efficacy Questionnaire for Children [baseline]

    It consists of 16 items rated on a 5-point Likert-type scale (not at all=1 to very well=5) with higher scores indicating higher self-efficacy.

  17. Self-efficacy Questionnaire for Children [at 6 week]

    It consists of 16 items rated on a 5-point Likert-type scale (not at all=1 to very well=5) with higher scores indicating higher self-efficacy.

  18. Self-efficacy Questionnaire for Children [at 12 week]

    It consists of 16 items rated on a 5-point Likert-type scale (not at all=1 to very well=5) with higher scores indicating higher self-efficacy.

Secondary Outcome Measures

  1. Emotional stress [baseline]

    the amount of cortisol in participants' hair.

  2. Emotional stress [at 6 week]

    the amount of cortisol in participants' hair.

  3. Emotional stress [at 12 week]

    the amount of cortisol in participants' hair.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Confirmed diagnosis (with proof of evidence) of UCP;

  • Aged between 12 and 18 years (younger children may lack the inductive reasoning skills to learn magic tricks);

  • Functional ability of the affected hand between levels I and III of the Manual Activity Classification System;

  • Intact cognition as indicated by a score above the corresponding cut-off point of the child's age on the Mini-Mental Examination for Children; and

  • Access to internet and a computer or smartphone that can perform videoconferencing.

Exclusion Criteria:
  • Severe hearing or visual impairments that prevent online learning;

  • Previous participation in organized magic learning program or camp;

  • Current or planned participation in an intensive upper limb intervention and/or new spasticity management (e.g., starting/increasing muscle relaxants, Botox injections) during the study period; or

  • Current or planned participation in psychological therapy or a clinical trial during the study period that could affect the outcomes of the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Alabama at Birmingham Birmingham Alabama United States 35294

Sponsors and Collaborators

  • University of Alabama at Birmingham

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hon K. Yuen, PhD, Professor, University of Alabama at Birmingham
ClinicalTrials.gov Identifier:
NCT05664841
Other Study ID Numbers:
  • 1909503-38
First Posted:
Dec 27, 2022
Last Update Posted:
Jan 23, 2023
Last Verified:
Jan 1, 2023
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 23, 2023