Internet Assisted Career-Oriented Soft-skills Training (iCareer) for Transition Age Youth with Mental Health Conditions: a Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to evaluate the effectiveness of an internet- assisted Career-Oriented Work-Related Soft-skills Training (iCareer) intervention, infused with cognitive behavioral therapy, targeting individuals ages 16-24 with mental health conditions, to improve employment outcomes. The overall objective is to help transition-age youth (TAY) with psychiatric disabilities achieve optimal employment outcomes as part of successful transition to adulthood. Findings will have implications for enhancing and developing pre-employment services for TAY with psychiatric disabilities.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 16
Maximum Age: 24
Healthy Volunteers: t
View:

• Age between 16 and 24 years

• Must speak English fluently

• Receiving Individualized Education Program (IEP)/504 Plan or disability services within the past 24 months with primary disability types of psychiatric disability

• No hospitalizations or suicide attempts within the past 2 months

• Willing to provide informed consent (if younger than 18, parental consent) to participate in the study

• Interested in improving work-related social skills

Locations
United States
New Jersey
Rutgers Univeristy, Newark- Office of Disability Services
RECRUITING
Newark
Contact Information
Primary
Weili Lu, PhD
luwe1@shp.rutgers.edu
908-889-2453
Backup
Janice Oursler, PhD
ourslejd@shp.rutgers.edu
908-889-2462
Time Frame
Start Date: 2023-06-23
Estimated Completion Date: 2027-03-01
Participants
Target number of participants: 126
Treatments
Experimental: Treatment
Soft Skills Training Intervention via telehealth
No_intervention: Control
Treatment as Usual (TAU)
Related Therapeutic Areas
Sponsors
Leads: Rutgers, The State University of New Jersey

This content was sourced from clinicaltrials.gov