Brief COVID-19 Intervention for People With Serious Mental Illness and Co-Morbid Medical Conditions
Study Details
Study Description
Brief Summary
The study will enroll 600 people with serious mental illness who receive services at Centerstone in KY or TN and will compare two different evidence-based self-management interventions: Integrated Illness Management and Recovery (I-IMR), a program developed by the study team at Dartmouth that trains people with serious mental illness on physical and mental health self-management, and the Stanford Chronic Disease Self-Management Program (CDSMP), a program largely focused on physical health self-management that has been used widely in the general population. In addition, PCORI is funding an evaluation of a COVID-related intervention that will begin in the Fall 2020.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Detailed Description
The proposed study will be the first to compare two commonly used but substantially different, evidence-based self-management interventions. Integrated Illness Management and Recovery (I-IMR), is an individually-tailored, 16-session, integrated program combining both physical and mental health self-management specifically developed for people with SMI. In contrast, the Stanford Chronic Disease Self-Management Program (CDSMP) is a group-based, 6-session, chronic disease self-management program largely focused on physical health self-management alone. I-IMR is delivered by community mental health providers or by community outreach workers, while CDSMP is co-delivered by two peers or by a health professional and a peer. Both programs have been widely recommended, disseminated, and used. The proposed parent study will randomize people with serious mental illness to I-IMR (n=300) and CDSMP (n=300).
Our COVID-related Enhancement will involve enrolling 150 participants from the parent project to an evaluation of an additional I-IMR module compared to usual care during the pandemic. The I-IMR module will be delivered by trained interventionists in 3 calls over 3 weeks to n=75 I-IMR participants. The I-IMR participants and CDSMP participants will continue to receive Usual Care, consisting of generic support calls from clinicians at the study sites. Baseline, and 6, 9, and 12 week assessments will evaluate the effectiveness of the COVID-19 module that will be added to I-IMR.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Integrated Illness Management and Recovery (I-IMR) PLUS COVID-19 ENHANCEMENT: In addition to the primary intervention (Integrated Illness Management and Recovery), participants received 3 additional COVID-19 related educational/skills training sessions provided individually, remotely by I-IMR Specialists. |
Behavioral: Integrated Illness Management and Recovery
Education and skills training groups on illness management of chronic medical and psychiatric illness. Subsample of 75 will also receive COVID-specific Integrated Illness Management and Recovery module.
|
Experimental: Stanford Chronic Disease Self-Management Program (CDSMP) ONLY: No additional COVID-19 intervention was provided to this group. These participants only received the primary disease management intervention (CDSMP) |
Behavioral: Chronic Disease Self-Management Program
Education and skills training groups on illness management of chronic conditions
|
Outcome Measures
Primary Outcome Measures
- Knowledge and Behaviors for Preventing Catching and Spreading COVID-19 Scale [Change from Baseline to 12 weeks]
Change in score on this measure, which was developed as part of the study plan because no suitable scale existed to assess knowledge and safety behaviors for COVID-19. Scores range from 0-100%, with higher scores indicating greater knowledge and enactment of safety behaviors.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Serious Mental Illness (diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder, or chronic depression with moderate impairment in functioning) receiving services at Centerstone(KY and TN)
-
Diagnosis of a chronic medical condition increasing risk of early mortality from cardiovascular or respiratory disease (e.g., diabetes, hyperlipidemia, hypertension, COPD, heart failure, tobacco dependence, obesity), and at least 1 ER visit or hospitalization within the past year or judgment by the treatment team of substantial need for illness self-management training.
Exclusion Criteria:
-
Consumers who do not speak English
-
Consumers with either no, or a well-controlled medical condition will not be included
-
Individuals residing in a nursing home or other institution
-
Evidence of significant cognitive impairment as indicated by a Mini Mental Status Examination score <24, will be excluded
Eligibility for the COVID -related substudy is dependent on enrollment and participation in the parent project (NCT03966872).
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Seven Counties Services | Louisville | Kentucky | United States | 40220 |
2 | Centerstone | Nashville | Tennessee | United States | 37228 |
Sponsors and Collaborators
- Dartmouth-Hitchcock Medical Center
- Patient-Centered Outcomes Research Institute
Investigators
- Principal Investigator: Sarah Pratt, PhD, Dartmouth-Hitchcock Medical Center
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- STUDY00031245