N/A
N=151
Project Bridge: Peer Health Navigator Intervention
Schizophrenia · Depression · Medical Disorders · Serious Mental Illness
Bottom Line
View on ClinicalTrials.gov: NCT02022462 ↗Enrolled (actual)
151
Serious AEs
0.0%
Results posted
Feb 2024
Primary outcome: Primary: Changed Score on SF-12 Pain Items From Baseline to 6 Months and 12 Months — -.16; .11; .19; -.18 Changed mean z-score — p=.073
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Health Navigation (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Southern California
- Primary completion
- Sep 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Changed Score on SF-12 Pain Items From Baseline to 6 Months and 12 Months |
-.16; .11; .19; -.18 | .073 |
| PRIMARY Changed Health Screenings From Baseline to 6 Months and 12 Months |
.44; .45; .17; .06 | .983 |
| PRIMARY Changed Number of Health Complaints From Baseline to 6 and 12 Months |
-1.07; -1.35; .78; -.94 | .731 |
| PRIMARY Changed Scores on Health Care Efficacy Scale From Baseline to 6 Months and 12 Months |
.06; .02; .13; -.02 | .244 |
| PRIMARY Changed Score on Primary Care Provider Relationship From Baseline to 6 and 12 Months |
-0.32; .08; .05; -.17 | .019 sig |
| SECONDARY Changed Scores on Provider Level Stigma From Baseline in Comparison to 6 and 12 Months |
.06; -.12; -.06; .13 | .203 |
| SECONDARY Changed Scores of General Life Satisfaction From Baseline to 6 and 12 Months |
.11; .12; .01; .04 | .897 |
| SECONDARY Changed Scores on BASIS-24 From Baseline in Comparison to 6 and 12 Months |
-.23; -.15 | .433 |
| SECONDARY Changed Unhealthy Habits From Baseline to 6 and 12 Months |
.18; .04; .07; -.16 | .228 |
| SECONDARY Changed Scores of Internalized Stigma From Baseline to 6 and 12 Months |
.07; .06; .01; .02 | .894 |
| SECONDARY ChangedPrescribed Medications From Baseline to 6 and 12 Months |
-.05; .10; .24; -.04 | .530 |
| SECONDARY Changed Number of Health Diagnoses From Baseline to 6 and 12 Months |
.23; -.08; .02; -.34 | .036 sig |
| SECONDARY Changed Euroqual Health Score From Baseline to 6 and 12 Months |
3.70; 3.29; -6.43; 7.12 | .931 |
| SECONDARY Changed Euroqual Satisfaction With Provider Score From Baseline to 6 and 12 Months |
6.32; 2.71; -1.06; 7.12 | .576 |
| SECONDARY Changed Substance Use From Baseline to 6 and 12 Months |
-.08; -.13; .04; -.11 | .792 |
| SECONDARY Changed Score on Self Management Motivation |
.33; -.28; .29; .57 | .049 sig |
Summary
The mortality rate among people with Serious Mental Illness (SMI) is 2 to 3 times that of the general population, meaning that those with a serious mental illness die, on average, 25 years earlier than those without an SMI. These deaths are largely attributed to preventable medical conditions, many of which are more common in the SMI population.
The "Bridge" intervention is a peer navigator model that was developed to target factors that negatively impact healthcare access, utilization, and outcomes among individuals with serious mental illness (e.g., severe mood disorders and psychotic disorders). This intervention targets male and female, adult consumers across races/ethnicities and has been utilized by Pacific Clinics (Southern California's largest behavioral healthcare agency) and the Department of Mental Health of Los Angeles County to improve the health and quality of life for their consumers.
Investigators will test the comparative effectiveness of a peer navigator intervention (the Bridge) to treatment as usual. The Bridge navigator intervention is designed to teach SMI consumers the skills to engage health care providers and to overcome motivational deficits in order to improve their health and healthcare use. The specific aims of this application are:
1. To use randomized methods to examine the effectiveness of the Bridge intervention on the health care utilization, satisfaction with care, health status, and health care self-management for a sample of individuals with severe mental illness receiving public mental health services in the community;
2. To use randomized methods to examine the effectiveness of the Bridge intervention on psychological and social well-being for a sample of individuals with severe mental illness receiving public mental health services in the community.
151 participants in an Full Service Partnership (FSP) clinic operated by Pacific Clinics were recruited to participate in an approximately 24-month long study of Bridge navigation. Participants will be randomly assigned to either treatment as usual (waitlist) or immediate intervention with the Bridge.
Participants in both groups will complete three assessments (baseline, 6 months, 12 months) and statistically compared over time. Staff stakeholders (n = 20) will also be interviewed at baseline and every three months of the study in order to ensure that the intervention is being implemented appropriately.
Eligibility Criteria
Inclusion Criteria
- Client participants will have diagnoses of serious mental illness and be between the ages of 18-65. All participants must be able to complete assessments in English.
- Staff participants will be between the ages of 18-65 and must be currently employed at Pacific Clinics. All participants must be able to complete assessments in English.
- Medical providers who serve clients of Pacific Clinics will also be interviewed as stakeholders. They will be between the ages of 18-65 and must be employees of a medical provider serving Pacific Clinics' clients.
Exclusion Criteria
- Clients who are under the age of 18, over the age of 65, who are under conservatorship, cannot give informed consent themselves, or are not receiving mental health services through Pacific Clinics will not be eligible for participation.
- Staff participants must be currently employed at Pacific Clinics and have the capacity to give informed consent themselves.
- Medical providers must be serving Pacific Clinics' clients and have the capacity to give informed consent themselves.
Data sourced from ClinicalTrials.gov (NCT02022462). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.