Depression Return to Work Intervention (DRIVEN)

October 16, 2024 updated by: Inspiration at Work

Developing an App-based Behavioral Intervention to Help Depressed Individuals Return to Work

This study is a randomized controlled trial to test the effectiveness of a mobile app-based program aimed to help individuals with unemployment-related emotional distress return to work.

Study Overview

Detailed Description

This study will compare two different approaches to reducing unemployment-related emotional distress. Participants will be involved in the study for a total of 22 weeks. During the first 6 weeks, participants will complete activities relating to either the mobile-app based program or the self-guided job-seeking program. The study team will follow up with participants at 8 weeks after the program is completed and at 16 weeks after the program is completed. Participants will also be asked to complete questionnaires before starting the program, during the program, after they complete the program, and at the follow-up visits. The questionnaires will be about the participant's mood, job seeking behavior, and related emotional experiences.

Study Type

Interventional

Enrollment (Actual)

141

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

    • Illinois
      • Chicago, Illinois, United States, 60614
        • Inspiration at Work, Inc.

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • 18-65 years of age
  • Currently unemployed and actively searching for work
  • Prior to unemployment, were employed full-time (35 hours per week or more) for at least 1 year
  • Prior to unemployment, received an individual highest salary of $100,000 or less
  • Owns an iPhone or Android Phone
  • Willing and able to provide informed consent
  • Has a minimum depression score according to the PROMIS depression scale
  • Able to communicate in English (verbal and written)

Exclusion Criteria:

  • Current moderate or severe alcohol/substance use disorders
  • Current symptoms of mania or psychosis
  • Currently employed, retired, or a full or part-time student

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: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: Conventional Job-Search Program
6 weeks of self-guided job-seeking
Participants will receive weekly information about job-searching skills and resources from a study coordinator for six weeks.
Experimental: DRIVEN App-Based Program
6 weeks of job-seeking guided by the DRIVEN curriculum
Participants will complete the six-week DRIVEN program, which includes a smartphone application and job coaching.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Job Search Behavior (JSB) Scale
Time Frame: Baseline; Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
10-item scale to assess the frequency that a person performs certain job seeking behaviors within a week. Each item has 5 answer options (from 0 times to 6 or more times). A higher score indicates that someone performs more job seeking behaviors each week.
Baseline; Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Job Search Self Efficacy (JSSE) Scale
Time Frame: Baseline; Week 3 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
20-item scale to assess someone's confidence in performing job seeking behaviors and achieving job seeking outcomes. Each item has 5 answer options (from 1 to 5). Raw scores of items from each domain are averaged to produce a final domain score between 1 and 5. A higher score indicates that someone is more confident in performing a job seeking behavior or achieving a job seeking outcome, depending on the domain.
Baseline; Week 3 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
The Inventory of Depression and Anxiety Symptoms (IDAS) - Social Anxiety Subscale
Time Frame: Baseline; Week 3 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
6-item scale to assess social anxiety symptoms. Each item has 5 answer options (from 1 to 5). A higher score indicates a greater presence of that symptom within the past two weeks.
Baseline; Week 3 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Patient Reported Outcome Measures Information System (PROMIS) Depression Scale
Time Frame: Baseline; Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
8-item scale to assess depression. Each item has 5 answer options (from 1 to 5). Minimum score = 8; maximum score = 40. A higher score indicates a greater presence of depressive symptoms.
Baseline; Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Patient Reported Outcome Measures Information System (PROMIS) Positive Affect Scale
Time Frame: Baseline; Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
15-item scale to assess positive affect. Each item has 5 answer options (from 1 to 5). Minimum score = 15; maximum score = 75. A higher score indicates a greater presence of positive affect.
Baseline; Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Patient Reported Outcome Measures Information System (PROMIS) Meaning and Purpose Scale
Time Frame: Baseline; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
8-item scale to assess meaning and purpose in someone's life. Each item has 5 answer options (from 1 to 5). Minimum score = 8; maximum score = 40. A higher score indicates a greater sense of meaning and purpose.
Baseline; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Cognitive Behavioral Avoidance Scale (CBAS)
Time Frame: Baseline; Week 5 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
31-item scale to assess what strategies someone uses to deal with situations and problems, with strategies falling into the domains of behavioral-social, cognitive-nonsocial, cognitive-social, and behavioral-nonsocial. Each item has 5 answer options (from 1 to 5). Raw scores of items from each domain are summed to produce a final domain score. A higher score indicates a greater presence of that coping strategy in someone's life.
Baseline; Week 5 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Behavioral Activation for Depression Scale (BADS)
Time Frame: Baseline; Week 5 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
9-item scale to assess behavioral activation. Each item has 7 answer options (from 0 to 6). Minimum score = 0; maximum score = 54. A higher score indicates higher activation.
Baseline; Week 5 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Cognitive Flexibility Inventory (CFI)
Time Frame: Baseline; Week 5 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
20-item scale to assess cognitive flexibility. Each item has 7 answer options (from 1 to 7). Minimum score = 20; maximum score = 140. A higher score indicates more cognitive flexibility.
Baseline; Week 5 of program; Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Participant Global Impression of Change (PGIC)
Time Frame: Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
To assess participant's impression of change in their depression since the start of the intervention. This scale is 1-item. Minimum score = 1; maximum score = 5. A higher score indicates the best change since starting the intervention.
Week 6 of program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
System Usability Scale (SUS)
Time Frame: Week 1 of program; Week 6 of program
10-item measure to assess the usability of the program. Each item has 5 answer options (from 1 to 5). Minimum raw score = 0; maximum raw score = 40. Raw scores are multiplied by 2.5 to give a final score of 0 (representing the worst usability) to 100 (representing the best usability).
Week 1 of program; Week 6 of program
Job Status Questionnaire
Time Frame: Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)
Measure to assess whether or not someone obtained a job throughout the course of the study.
Each week of the program; Follow-up (8 weeks after program); Follow-up (16 weeks after program)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Alexandra R. Levit, Inspiration at Work
  • Principal Investigator: Stewart A. Shankman, PhD, Northwestern University, Department of Psychiatry and Behavioral Sciences
  • Principal Investigator: James W. Griffith, PhD, University of Chicago

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)

August 7, 2023

Primary Completion (Actual)

September 28, 2024

Study Completion (Actual)

September 28, 2024

Study Registration Dates

First Submitted

August 30, 2023

First Submitted That Met QC Criteria

August 30, 2023

First Posted (Actual)

September 7, 2023

Study Record Updates

Last Update Posted (Actual)

October 18, 2024

Last Update Submitted That Met QC Criteria

October 16, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • R42MH127971 (U.S. NIH Grant/Contract)

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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