- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06026280
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
Status
Completed
Conditions
Intervention / Treatment
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.
Sponsor
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
Keywords
Additional Relevant MeSH Terms
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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