- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05066906
Videogame-based Tool for Job Search and Executive Function Improvement in Adults With ASD
Assessing Videogame-Based Tool for Job Search and Executive Function Improvement in Adults With Autism Spectrum Disorder
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- IQ above 60
- Diagnosis of ASD as confirmed by qualified clinician (including Dr. Fung), and if necessary the administration of Autism Diagnostic Interview-Revised (ADI-R) and/or Autism Diagnostic Observation Schedule-Generic (ADOS-G)
- Age 18 to 55
- Adults who are physically healthy
- able to travel to work independently
Exclusion Criteria:
- DSM-5 diagnosis of other severe psychiatric disorder such as schizophrenia
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Device Feasibility
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Use of Identifor and Companion+referral to employment agencies
This group will use the Identifor tool and Companion app for a period of 6 months.
They will also receive standard referral to employment agencies.
|
Identifor pinpoints what players excel at by using objective metrics and quantifiable data to collect information relevant to employment, including Multiple Intelligence, Executive Function, and personality themes. Companion is a 24/7 personalized aide for teens and adults iwth special needs that uses and artificial intelligence avatar to have back-and-forth conversations with users in a meaningful way to support the user in different domains of their everyday lives including public transit, managing personal schedules, and money management.
Standard referral to employment agencies based on an individual's background, skillset, and preferences
|
|
Active Comparator: Referral to employment agencies
This group will not use the Identifor tool and Companion app.
They will only receive standard referral to employment agencies.
|
Standard referral to employment agencies based on an individual's background, skillset, and preferences
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Rate of securing internship, part-time, or full-time positions
Time Frame: 6 months after initiation of referral
|
Percentage of participants securing internship, part-time, or full-time positions
|
6 months after initiation of referral
|
|
Level of satisfaction
Time Frame: 3 months after initiation of referral
|
The level of participant satisfaction will be determined from a Likert scale ("Very satisfied", "Somewhat satisfied", "Neither satisfied nor dissatisfied", "Somewhat dissatisfied", and "Very dissatisfied").
|
3 months after initiation of referral
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavior Rating Inventory of Executive Function for Adults (BRIEF-A)
Time Frame: 6 months after initiation of referral
|
measure of executive function for adults
|
6 months after initiation of referral
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Lawrence Fung, MD,PhD, Stanford University
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB-52313
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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