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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04980963
Other study ID # 20-069
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2020
Est. completion date June 30, 2024

Study information

Verified date July 2021
Source Kent State University
Contact Mykal Leslie, PhD
Phone 3306725798
Email mleslie8@kent.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will fill important knowledge gaps in the availability of best practices that use innovative methods to integrate the cognitive and vocational needs of students with Autism Spectrum Disorder (ASD) who will be transitioning from 2- and 4-year postsecondary education to employment. Best practices exist from the assistive technology (AT) field to help people compensate for cognitive impairments, and from the vocational rehabilitation (VR) field to enhance employment outcomes for individuals with disabilities. However, these practices have not been integrated to provide needed supports and services to improve the employment outcomes of students with ASD. The study's goal is to expand the availability of innovative practices by testing the efficacy of a technology-driven, long-term, and resource-rich individualized support program that merges assistive technology for cognition and vocational rehabilitation practices. The end products will include technology application guidelines, training and procedural manuals, and resource information that rehabilitation professionals and students with ADS can utilize to enhance technology and mentoring proficiency, academic success, self-determination, and long-term career success for students with ASD. The knowledge to be gained from this research will have a beneficial impact on students with ASD, rehabilitation professionals, higher education personnel, case managers, and employers who work with people with ASD. There is strong potential for the students to develop skills that will help them succeed in learning as well as employment settings. The ultimate benefit of research activities for the target population will be seen in the improved capacity for postsecondary students with ADS to utilize state-of-the-art technology to accommodate disability-related limitations, address career readiness, and to prepare for and obtain employment after graduation. Because the risks to subjects are no greater than those associated with everyday life and because the study staff will refer students who are in psychological distress or medical emergency situations to appropriate resources in the community, the minimal risks of this study justify the considerable benefits that this study will yield. Not only will the study benefit participating students, it stands to make important contributions to the knowledge bases in the fields of assistive technology and rehabilitation.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date June 30, 2024
Est. primary completion date June 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Must be a post-secondary student enrolled in degree programs at two-year and four-year colleges or universities within a 60-mile radius of Kent, Ohio - Must have a clinical diagnosis of Autism Spectrum Disorder Exclusion Criteria: - No other exclusion criteria will be applied

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Cognitive Support Technology (CST)
Cognitive Support Technology (CST) products and strategies are used to help people with disabilities compensate for or accommodate cognitive limitations (including those related to interpersonal communication and social cognition) that present difficulties for them in the performance of desired social roles, especially education and employment. CSTs may be mainstream everyday technologies such as tablet computers or they may be specialized devices designed for specific goals such as step-by-step instruction in the performance of a particular task (Scherer, 2012).

Locations

Country Name City State
United States Kent State University Kent Ohio

Sponsors (2)

Lead Sponsor Collaborator
Kent State University Virginia Commonwealth University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Grade Point Average (GPA) Participant GPA Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Current academic standing Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Post-Secondary Enrollment Status % of participants still enrolled in a postsecondary program Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Satisfaction with current living status and transportation access Measured using single item 5-point Likert question on questionnaire Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Satisfaction with Social Support Measured using single item 5-point Likert question on questionnaire Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Current Employment Status Three items on questionnaire including dichotomous employment question (e.g., are you employed?), if yes, number of hours employed and weekly earnings. Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary % of Participants Receiving Disability Benefits Whether participants receive SSDI and/or SSI benefits or not Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Depression Symptoms Measured using Beck Depression Inventory- II (BDI-II) Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Overall Health Status Measured using RAND 36-item Health Survey Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Perceived Stress Measured using Perceived Stress Scale- 10 Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Acceptance of Disability Measured using the Acceptance of Disability Scale- Short Form Baseline (enrollment in study), 6 months, and 1 year (study completion)
Secondary Quality of Life (QoL) Measured using the Qualify of Life Scale Baseline (enrollment in study), 6 months, and 1 year (study completion)
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