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A Self-guided App-Based Virtual Reality Cognitive Behavior Therapy for Anxiety Disorder in Children

Primary Purpose

Anxiety Disorders

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
0-anxiety
Sponsored by
Universidade Federal do Rio de Janeiro
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anxiety Disorders focused on measuring anxiety, virtual reality, app, self-guided, Cognitive behavior therapy

Eligibility Criteria

8 Years - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • individuals must be between 8-12 years old;
  • subjects must score above 25 on the SCARED questionnaire;
  • subjects must have access to a smart phone and internet;
  • individuals must be willing to participate in the research study and providing informed consent.

Exclusion Criteria:

  • children that present with symptoms of severe depression or suicidality as measured with KSADS-PL26;
  • children that have insufficient knowledge of the Portuguese language;
  • subjects that are under any current treatment for anxiety disorder or using psychotropic medication.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    0-anxiety

    wait-list condition

    Arm Description

    0-anxiety is based on the principles of VRT and CBT, which currently is the most researched and used treatment for anxiety disorders. The 0-anxiety intervention is an app-based intervention consisting of six modules that can be followed according to a user's own timing and without the intervention of a therapist.

    Outcomes

    Primary Outcome Measures

    Anxiety levels
    Screen for Child Anxiety Related Disorders (SCARED). A score above 25 indicates a significant level of anxiety. Higher scores mean worse anxiety levels.

    Secondary Outcome Measures

    Fear Survey Schedule for Children-Revised (FSSC-R)
    The FSSC-R is a widely used self-report measure of children and adolescents' fears. The instrument, a revision of Scherer and Nakamura's (1968) original Fear Survey Schedule for Children, contains 80 items that are each rated on a three-point scale (none, some, a lot). A total fearfulness score can be obtained, as can five subscale scores based on a factor analysis of the items. In addition, the number of intense fears can be indicated (i.e., the number of fears endorsed 'a lot'), as can the most prevalent fears for a given child/adolescent or group of children and adolescents (i.e., boys, preadolescents, school phobic youngsters, etc.). Higher scores mean worse fear levels.
    Spence Children's Anxiety Scale - Parent and Children version
    The scale is completed by a parent of an anxious child between the ages of 6 to 18. It provides an overall measure of anxiety together with scores on six sub-scales each tapping a specific aspect of child anxiety. - Panic attack and agoraphobia - Separation anxiety - Physical injury fears - Social phobia - Obsessive compulsive - Generalized anxiety disorder / overanxious disorder. This yields a maximum possible score of 114. Higher scores mean worse anxiety levels.

    Full Information

    First Posted
    April 25, 2021
    Last Updated
    April 27, 2021
    Sponsor
    Universidade Federal do Rio de Janeiro
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04868201
    Brief Title
    A Self-guided App-Based Virtual Reality Cognitive Behavior Therapy for Anxiety Disorder in Children
    Official Title
    A Self-guided App-Based Virtual Reality Cognitive Behavior Therapy for Anxiety Disorder in Children
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 1, 2021 (Anticipated)
    Primary Completion Date
    February 1, 2023 (Anticipated)
    Study Completion Date
    February 1, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Universidade Federal do Rio de Janeiro

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    To examine the efficacy of a fully self-guided app-based virtual reality cognitive behavior therapy (VR CBT) using low-cost (cardboard) virtual reality goggles compared with a wait-list control group and to determine its user friendliness. We hypothesize that children with GAD enrolled in the self-guided app will present lower scores of anxiety.
    Detailed Description
    A randomized controlled design will be carried out, in which the effectiveness and user- friendliness of an online app-based VR self-help treatment '0-anxiety' will be evaluated. Our primary objective is to determine the clinical effects (a reduction in anxiety symptoms at post-test [between the experimental condition and controls] of 0-anxiety, and whether effects are sustainable at follow-up [a reduction in anxiety symptoms between baseline and follow-up for those in the experimental condition]). Our secondary objective is to determine the user-friendliness of 0-anxiety. In this study, 230 children from the Brazilian population will be randomized over 2 conditions: the experimental condition (0-anxiety) and a waitlist condition. The duration of the intervention will be 3 weeks. Measures will be taken at baseline, directly after the intervention (3 weeks) and at 3 months (follow-up). All measures will be completed online. Therefore, the child will participate in the study in his/her natural environment. Subjects in the wait-list condition will receive the intervention after completion of the post-test. Randomization (block-randomization) will be performed by an independent researcher.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Anxiety Disorders
    Keywords
    anxiety, virtual reality, app, self-guided, Cognitive behavior therapy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Care ProviderOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    230 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    0-anxiety
    Arm Type
    Experimental
    Arm Description
    0-anxiety is based on the principles of VRT and CBT, which currently is the most researched and used treatment for anxiety disorders. The 0-anxiety intervention is an app-based intervention consisting of six modules that can be followed according to a user's own timing and without the intervention of a therapist.
    Arm Title
    wait-list condition
    Arm Type
    No Intervention
    Intervention Type
    Device
    Intervention Name(s)
    0-anxiety
    Intervention Description
    0-anxiety is a self-guided app-based utilizing virtual reality establish in cognitive behavior therapy treatment.
    Primary Outcome Measure Information:
    Title
    Anxiety levels
    Description
    Screen for Child Anxiety Related Disorders (SCARED). A score above 25 indicates a significant level of anxiety. Higher scores mean worse anxiety levels.
    Time Frame
    baseline and and 3 months after the completion of the intervention
    Secondary Outcome Measure Information:
    Title
    Fear Survey Schedule for Children-Revised (FSSC-R)
    Description
    The FSSC-R is a widely used self-report measure of children and adolescents' fears. The instrument, a revision of Scherer and Nakamura's (1968) original Fear Survey Schedule for Children, contains 80 items that are each rated on a three-point scale (none, some, a lot). A total fearfulness score can be obtained, as can five subscale scores based on a factor analysis of the items. In addition, the number of intense fears can be indicated (i.e., the number of fears endorsed 'a lot'), as can the most prevalent fears for a given child/adolescent or group of children and adolescents (i.e., boys, preadolescents, school phobic youngsters, etc.). Higher scores mean worse fear levels.
    Time Frame
    baseline, 3 weeks after the intervention, and 3 months after the completion of the intervention
    Title
    Spence Children's Anxiety Scale - Parent and Children version
    Description
    The scale is completed by a parent of an anxious child between the ages of 6 to 18. It provides an overall measure of anxiety together with scores on six sub-scales each tapping a specific aspect of child anxiety. - Panic attack and agoraphobia - Separation anxiety - Physical injury fears - Social phobia - Obsessive compulsive - Generalized anxiety disorder / overanxious disorder. This yields a maximum possible score of 114. Higher scores mean worse anxiety levels.
    Time Frame
    baseline, 3 weeks after the intervention, and 3 months after the completion of the intervention

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    8 Years
    Maximum Age & Unit of Time
    12 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: individuals must be between 8-12 years old; subjects must score above 25 on the SCARED questionnaire; subjects must have access to a smart phone and internet; individuals must be willing to participate in the research study and providing informed consent. Exclusion Criteria: children that present with symptoms of severe depression or suicidality as measured with KSADS-PL26; children that have insufficient knowledge of the Portuguese language; subjects that are under any current treatment for anxiety disorder or using psychotropic medication.

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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    A Self-guided App-Based Virtual Reality Cognitive Behavior Therapy for Anxiety Disorder in Children

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