Diabetes Mellitus, Type 2
Conditions
Keywords
THRIVE-DM, Community-based organizations, Triage
Brief summary
The goal of this study is to develop, implement, and evaluate a patient-centered triage and referral model designed to improve health outcomes for individuals with uncontrolled type 2 diabetes mellitus (T2DM) and unmet health-related social needs. The intervention builds on the existing THRIVE infrastructure at Boston Medical Center (BMC), which includes screening for social needs and a resource referral guide. It integrates medical and social care by embedding a data-driven triage tool within the EPIC electronic health record system, engaging community health workers trained in population health, and initiating closed-loop EPIC integrated referrals to community-based organizations. This study will use a hybrid type 3 effectiveness-implementation trial design to evaluate the implementation of the THRIVE-DM intervention at the clinic level. Preliminary effectiveness will be assessed by comparing THRIVE-DM to usual care in its ability to increase patient connections to community-based organizations and improve clinical outcomes. Using a stratified randomization approach, the investigators will compare referral closure rates, receipt of social services, hemoglobin A1C levels, and patterns of health service utilization between patients enrolled in THRIVE-DM and those receiving standard care
Interventions
OTHERTHRIVE-DM
Low-SS and High-SS will be referred by the CHW to appropriate community-based organizations through the THRIVE Directory. High-SS participants will also receive additional support from a patient navigator (PN), who will follow up to facilitate service connection and address barriers to engagement. CHWs and PNs will coordinate care to ensure services are aligned with the patient's assessed needs.
OTHERStandard of care
Standard of care may include support from the primary care team, health related social needs (HRSN) screening via the THRIVE screener, printed resource guides, and referrals to community-based organizations initiated at the discretion of clinic staff using the THRIVE Directory.
Sponsors
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Boston Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Intervention model description
Eligible participants will be categorized into low social services need (Low-SS) and high social services need (High-SS) and then randomized into intervention or control arms using block randomization in REDCap.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Diagnosis: Must have a diagnosis of Type 2 Diabetes Mellitus (T2DM), confirmed by a current diagnosis in the medical record or at least two billing codes in the last two years, or an HbA1c level ≥6.5% in the last two years. * Uncontrolled T2DM: Must have an HbA1c ≥9% at the time of screening. * Health-Related Social Needs: Must have been screened for health related social needs (HRSNs) during a General Internal Medicine (GIM) visit in the last 3 months and screened positive for at least one HRSN.
Exclusion criteria
* Patients enrolled in Complex Care Management (CCM). * Patients receiving hospice care. * Patients who are deceased * Patients with Type 1 Diabetes Mellitus (T1DM).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants that connect to Community-Based Organizations | 3 months, 6 months, 3 months post intervention | Connection to Community-Based Organizations will be assessed through several sources and documented in REDCap |
| Number of participants that are helped by Community-Based Organizations | 3 months, 6 months, 12 months post intervention | Data will be collected from participant interviews |
| Changes in HbA1c | 3 months, 6 months, 12 months post intervention | HbA1c data will be extracted from the EPIC electronic health record (EHR). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of participants hospitalized | 3 months, 6 months, 12 months post intervention | Data will be obtained from the EHR. |
| Number of participants that had an emergency department visit | 3 months, 6 months, 12 months post intervention | Data will be obtained from the EHR. |
Countries
United States
Contacts
Primary ContactMichael Fischer, MD
Backup ContactUma Khemraj, MS
Outcome results
None listed