WORKWELL: Cognitive Behavioral Therapy to Improve Work and Wellness in Veterans With Mental Illness

Sponsor
VA Office of Research and Development (U.S. Fed)
Overall Status
Recruiting
CT.gov ID
NCT04504903
Collaborator
(none)
278
3
2
44.9
92.7
2.1

Study Details

Study Description

Brief Summary

Vocational instability in Veterans with serious mental illness (SMI) is pervasive, costly, and harmful. Over 75% of Veterans with SMI are unemployed, resulting in economic difficulties and trouble meeting basic needs. Overall, among adults with depression, work dysfunction results in a 36 to 51 billion dollar loss annually. Unemployed Veterans with SMI also suffer major health consequences, including a more severe course of illness and poor recovery over time, leading to increased inpatient and emergency service use. The WORKWELL study will synergistically address these deficits in health, recovery, and work functioning by testing the Cognitive Behavioral Therapy for Work Success (CBTw) intervention. Using a pragmatic design, this project will address work as a major social determinant of health and close the health disparity gap among people with SMI. Further, through promotion of work and healthy thinking, CBTw holds promise to reduce risk of suicide among vulnerable veterans with SMI.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Behavioral Therapy For Work Success (CBTw)
  • Behavioral: Psychoeducation
N/A

Detailed Description

Project background: Work is a major social determinant of health. In people with serious mental illness (SMI), work is associated with better wellbeing, physical and mental health, quality of life, and may prevent the onset of disability. Among Veterans with SMI, work is a protective factor against suicide.

Most veterans with SMI are unemployed and suffer substantially worse health and recovery across key domains. Despite quality VHA vocational services, such as supported employment (SE), two-thirds or more of Veterans who receive these services experience work dysfunction. A probable explanation lies in unsolved cognitive and behavioral barriers, such as low work-related self-efficacy, ineffective coping skills, little hope that work is attainable, poor work motivation and sense of self.

The Cognitive Behavioral Therapy for Work Success (CBTw) intervention was designed to target these problems and augment VHA SE services to synergistically improve work, as well as health and recovery, in Veterans with SMI. In an open trial pilot, CBTw was associated with significant increases in hours worked and wages earned and the majority of CBTw participants became steady workers. Veterans also experienced improvements in symptoms, recovery, and quality of life.

Project goals: Using Hybrid 1 RCT design, this project will test the effects of CBTw on competitive work and health and recovery outcomes over a 9-month study period at 3 VA SE programs. Informed by the RE-AIM framework, an implementation evaluation will examine the success of using SE staff to deliver CBTw, barriers and facilitators to implementation, and strategies utilized.

Relevance to priorities: This project has high implementation potential and is responsive to the VHA priority regarding Health Equity, as it will address work functioning, an under studied social determinant of health. WORKWELL also holds promise to improve health and recovery outcomes among Veterans with SMI, another HSR&D area of emphasis. Lastly, this study is consistent with the goal of finding novel strategies toward suicide prevention among vulnerable Veteran groups, including those with SMI.

Objectives: Aim 1: Test the effects of CBTw + SE compared to a control of psychoeducation + SE on work. Hypotheses: Participants in the CBTw+ SE arm will work significantly more total weeks in competitive jobs (primary study outcome) and will be more likely to become steady workers.

Aim 2: Test the effects of CBTw + SE on health and recovery. Hypotheses: Participants in the CBTw + SE arm will have greater improvements on subjective recovery and health-related quality of life, and decreases in symptoms, suicidal ideation, and inpatient service utilization.

Aim 3: Guided by the RE-AIM implementation science framework, conduct an evaluation of the implementation of CBTw, including examination of the feasibility of using SE staff to deliver CBTw, and related barriers and facilitators. The objective is to spur future wide scale CBTw implementation.

Project Methods: WORKWELL is a pragmatic, Hybrid 1 design RCT. CBTw will be tested at 3 SE sites-Roudebush VA Medical Center, the Edward J. Hines VA Medical Center, and the VA St. Louis Health Care System. 276 unemployed Veterans with SMI will be randomly assigned to receive CBTw plus SE or a control of psychoeducation plus SE. Outcomes including total weeks worked in competitive jobs (primary), achievement of steady work, symptoms, recovery, health related quality of life, suicidal ideation, and service utilization will be assessed at posttreatment (12 weeks), 6 months (primary endpoint), and 9 months (to examine sustained effects). CBTw implementation planning, training, and consultation will be provided. CBTw implementation (fidelity), barriers and facilitators to implementation, and other RE-AIM elements will be examined using mixed methods.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
278 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Unemployed participants with serious mental illness will be randomized to receive group-based cognitive behavioral therapy geared toward improving competitive work outcomes or a time and format matched psychoeducation interventionUnemployed participants with serious mental illness will be randomized to receive group-based cognitive behavioral therapy geared toward improving competitive work outcomes or a time and format matched psychoeducation intervention
Masking:
Single (Outcomes Assessor)
Masking Description:
Research personnel conducting outcomes assessments will be blinded to condition assignment
Primary Purpose:
Treatment
Official Title:
Work as a Determinant of Health: A Pragmatic Trial of Enhanced Cognitive Behavioral Therapy to Bolster Competitive Work and Wellness in Veterans With Serious Mental Illness (WORKWELL)
Actual Study Start Date :
Jan 1, 2021
Anticipated Primary Completion Date :
Sep 30, 2024
Anticipated Study Completion Date :
Sep 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cognitive Behavioral Therapy For Work Success (CBTw)

Veterans will participate in 12 weekly group sessions to discuss thoughts, feelings, and behaviors that promote work success in the community

Behavioral: Cognitive Behavioral Therapy For Work Success (CBTw)
Veterans will go to 12 weekly group sessions and will learn healthy thinking about work, positive behavioral coping related to work, and will form a work success plan based on their work goals.

Active Comparator: Psychoeducation

Veterans in the control group will participate in 12 weekly group sessions in which they will learn more about their mental health conditions.

Behavioral: Psychoeducation
Veterans will go to 12 weekly group sessions and will learn more information about their mental health conditions. Psychoeducation modules are from the Illness Management and Recovery program.

Outcome Measures

Primary Outcome Measures

  1. Total weeks worked in competitive jobs change [baseline to 6 months]

    Outcome measure will be mean number of weeks worked in competitive jobs. The primary endpoint is 6 months (primary comparison will be baseline to 6 months). Competitive jobs are regular jobs open to all that pay at least minimum wage. More total weeks worked in competitive jobs is indicative of a positive outcome.

Secondary Outcome Measures

  1. Achievement of steady competitive work change [baseline to 9 months]

    Outcome measure of steady competitive work is defined as working at least 50% of the study period as assessed at the 9 month follow up period. Achievement of steady competitive work is a positive outcome.

  2. Cross-Cutting Symptom Measure (CCSM) change [baseline to 6 months]

    Outcome measure is a 23-item, Likert response (scored on a 0 to 4 scale), self-rated instrument that assesses 13 domains of psychiatric symptoms(e.g., depression, anxiety, psychosis, mania, sleep problems, self-harm, substance use, etc.) with higher scores indicating more severe total symptoms. Total scores range from 0 to 92.

  3. 12-item Short Form Survey (SF-12) change [baseline to 6 months]

    The SF-12 outcome measure will assess health-related quality of life and is comprised of the Physical Component Summary (PCS) and Mental Component Summary (MCS). Total scores range from 0 to 100 with higher scores indicating higher health-related quality of life.

  4. Scale for Suicidal Ideation change [baseline to 6 months]

    Outcome measure is a 21-item interviewer rated measure of a continuum of suicidal ideation, including thoughts, attitudes, plans, and behaviors. Total scores range from 0 to 42 with higher scores indicating more suicidal ideation.

  5. Recovery Assessment Scale change [baseline to 6 months]

    Outcome measure is a 41 item self report survey that will assess subjective recovery attitudes. Total scores range from 41 to 164 with higher scores indicating higher levels of subjective recovery.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Unemployment, defined as no current participation in a competitive job

  • A competitive work goal, which denotes a goal of a regular job in the community that pays at least minimum wage

  • Presence of a serious mental illness including one or more of the following conditions:

  • major depression

  • bipolar disorders

  • schizophrenia

  • schizoaffective disorder

  • posttraumatic stress disorder (PTSD)

  • Currently enrolled in and receiving VA vocational rehabilitation services

Exclusion Criteria:
  • Previous participation in cognitive behavioral therapy intervention geared toward work

  • Presence of a severe medical or cognitive impairment that will prevent participation in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Edward Hines Jr. VA Hospital, Hines, IL Hines Illinois United States 60141-5000
2 Richard L. Roudebush VA Medical Center, Indianapolis, IN Indianapolis Indiana United States 46202-2884
3 St. Louis VA Medical Center John Cochran Division, St. Louis, MO Saint Louis Missouri United States 63106

Sponsors and Collaborators

  • VA Office of Research and Development

Investigators

  • Principal Investigator: Marina Elizabeth Kukla, PhD MS BS, Richard L. Roudebush VA Medical Center, Indianapolis, IN
  • Principal Investigator: Jay Mendell, MS, St. Louis VA Medical Center John Cochran Division, St. Louis, MO
  • Principal Investigator: Kenneth C Weber, MEd, Edward Hines Jr. VA Hospital, Hines, IL

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
VA Office of Research and Development
ClinicalTrials.gov Identifier:
NCT04504903
Other Study ID Numbers:
  • IIR 19-176
First Posted:
Aug 7, 2020
Last Update Posted:
Jan 14, 2022
Last Verified:
Dec 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by VA Office of Research and Development
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 14, 2022