- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04771338
Examining the Effects of a Job Entry Intervention (IMPRESSIVE)
January 15, 2024 updated by: Helen Genova, Kessler Foundation
The current study will examine the efficacy of a virtual reality (VR) intervention as well as a newly developed Kessler Foundation STRength IDentification and Expression tool (VR-STRIDE) with adolescents diagnosed with autism spectrum disorder.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The current study will examine the efficacy of a virtual reality (VR) intervention entitled "IMPRoving Expression of Skills and Strengths In Interviewing in a Virtual Environment" (IMPRESSIVE) which targets social competency skills needed for successful job interviewing.
Specifically, 2 VR tools are utilized in the IMPRESSIVE intervention.
The first tool is VR-Job Interview Training, a VR program which offers the opportunity for repeated practice with a virtual human interviewer.
Preliminary evidence suggests that the VRprogram is successful in adults with ASD and schizophrenia in improving interview abilities.
However, the efficacy of it has not been evaluated in adolescents with ASD.
This represents a significant void in our knowledge, as we do not know whether this program is effective for youth.
In addition to VR training, a newly developed tool is included in the currently proposed intervention: the Kessler Foundation STRength IDentification and Expression tool (VR-STRIDE).
KF-STRIDE is focused on improving the ability to express personal strengths during the job interview, a skill that is not taught with VR training.
The proposed IMPRESSIVE intervention, which combines the learning of 2 critical abilities (social skills and strength identification), has never been examined in individuals with ASD.
Thus, the current proposal will be the first to examine the efficacy of these 2 combined tools in this at-risk population.
Study Type
Interventional
Enrollment (Actual)
34
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New Jersey
-
East Hanover, New Jersey, United States, 07936
- Kessler Foundation
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
12 years to 14 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Diagnoses of ASD
- or am a typically developing adolescent
- Able to speak and read English fluently
Exclusion Criteria:
- History of stroke, traumatic brain injury, or any other neurological injury or disease
- History of significant psychiatric illness (bipolar, schizophrenia or psychosis)
- Uncontrolled seizures
- Any other unstable medical complications
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Treatment group
Job interview training protocol for 12 sessions
|
Treatment group will receive 12 sessions of job interview training protocol.
Other Names:
|
|
No Intervention: Control group
No participation in any intervention protocol
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mock Job Interview Change
Time Frame: 8 weeks
|
Mock Job Interview skills will be assessed by having blinded raters trained to assess job interviews scoring participants across a number of domains including expressing personal strengths and sounding professional.
This rating scheme has been used in previous research (Smith et al., 2014; 2015),
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Self-reported job interview skills
Time Frame: 8 weeks
|
Questionnaire to assess self-perceived skills
|
8 weeks
|
|
self-reported job interview anxiety
Time Frame: 8 weeks
|
Questionnaire to assess self-perceived anxiety
|
8 weeks
|
|
Employment readiness
Time Frame: 8 weeks
|
Questionnaire to assess self-perceived employment readiness
|
8 weeks
|
|
Job Search Behavior
Time Frame: 8 weeks
|
Questionnaire to assess self-perceived job search behaviors
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Helen Genova, PhD, Kessler Foundation
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 1, 2019
Primary Completion (Actual)
June 22, 2022
Study Completion (Actual)
July 26, 2023
Study Registration Dates
First Submitted
February 23, 2021
First Submitted That Met QC Criteria
February 23, 2021
First Posted (Actual)
February 25, 2021
Study Record Updates
Last Update Posted (Actual)
January 17, 2024
Last Update Submitted That Met QC Criteria
January 15, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R-1078-19
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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