Modifying (Phase I) and Evaluating (Phase II) Virtual Reality Job Interview Training for Youth in Transition
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT03514134 |
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Recruitment Status :
Active, not recruiting
First Posted : May 2, 2018
Last Update Posted : January 6, 2022
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Autism Spectrum Disorder | Behavioral: Virtual Reality Job Interview Training Behavioral: Services as Usual | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 71 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Single (Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Modifying (Phase I) and Evaluating (Phase II) Virtual Reality Job Interview Training for Youth |
| Actual Study Start Date : | October 1, 2018 |
| Actual Primary Completion Date : | May 20, 2021 |
| Estimated Study Completion Date : | July 1, 2022 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Services as usual + Virtual Reality Job Interview Training
In addition to the services as usual comparator, participants will participate in Virtual Reality Job Interview Training.
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Behavioral: Virtual Reality Job Interview Training
Students will engage in didactic training related to strategies to perform well during a job interview as well as repeated practice with a virtual hiring manager. Throughout and after completion of the virtual interviews, participants will receive feedback on their performance. Behavioral: Services as Usual Study participants will be receiving their community-based or school-based services as usual that may include but is not limited to vocational skill training, daily living skill training, and social skill training. |
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Active Comparator: Services as Usual
Study participants will be receiving their community-based or school-based services as usual that may include but is not limited to vocational skill training, daily living skill training, and social skill training.
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Behavioral: Services as Usual
Study participants will be receiving their community-based or school-based services as usual that may include but is not limited to vocational skill training, daily living skill training, and social skill training. |
- Change in Job Interview Skills [ Time Frame: Collected at Pre-Test and Post-Test visits (within approximately 1 month of active treatment) ]Performance on 2 Mock Job Interviews
- Change in Job Interview Self-Efficacy [ Time Frame: Collected at Pre-Test and Post-Test visits (within approximately 1 month of active treatment) and 6 month follow-up ]9 item self-report
- Change in Job Interview Motivation [ Time Frame: Collected at Pre-Test and Post-Test visits (within approximately 1 month of active treatment) and 6 month follow-up ]7 item self-report
- Change in Job Interview Anxiety [ Time Frame: Collected at Pre-Test and Post-Test visits (within approximately 1 month of active treatment) and 6 month follow-up ]15 item self-report
- Change in Employment Outcomes [ Time Frame: Collected at pre-test and at 6 months after completing Post-Test Visit ]Obtained a part-time or full-time community-based job; time to employment
- Change in Depressive Symptoms [ Time Frame: Collected at Pre-Test and Post-Test visits (within approximately 1 month of active treatment) and 6 month follow-up ]mental health assessment
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 16 Years to 21 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Diagnosis of autism based on school records or the social responsiveness scale version 2
- at least a 4th grade reading level
- Currently enrolled in transition services and/or presents with an individualized educational plan
Exclusion Criteria:
- Unwilling to be videorecorded during primary outcome mock interviews
- Parents unwilling to provide informed consent
- unwillingness to provide minor assent
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03514134
| United States, Michigan | |
| University of Michigan | |
| Ann Arbor, Michigan, United States, 48109-1106 | |
| Principal Investigator: | Matthew Smith, PhD | University of Michigan |
| Responsible Party: | Matthew Smith, Associate Professor, University of Michigan |
| ClinicalTrials.gov Identifier: | NCT03514134 |
| Other Study ID Numbers: |
HUM00129575 |
| First Posted: | May 2, 2018 Key Record Dates |
| Last Update Posted: | January 6, 2022 |
| Last Verified: | January 2022 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Autism Spectrum Disorder Child Development Disorders, Pervasive Neurodevelopmental Disorders Mental Disorders |

