Community Integration, Patient Engagement
Conditions
Brief summary
This project will engage patients and health care teams to develop, implement, and rigorously evaluate a new lay health worker role (Community Resource Specialist, CRS) for primary care teams. The CRS will link patients and healthcare clinics with community resources.
Detailed description
Patients are served best when multiple organizations work together to meet healthcare needs. In the Chronic Care Model, community resources supplement productive interactions between patients and care teams. However, healthcare delivery systems and health research have given relatively little attention to the model's community features. This project engages patients in designing a primary care community liaison role (Community Resource Specialist, CRS) connecting patients to clinic and community resources that support chronic disease prevention and management. The CRS role will enhance primary care by better integrating community resources into patient care. The proposed design effort will: * develop tools and work processes that promote meaningful patient engagement in creating a CRS concept and role * integrate the CRS role into primary care teams * assess effects of this role on patient-centered outcomes. The patient engagement process will use principles from Lean, a quality improvement method, to engage all primary care stakeholders, particularly patients and clinical staff. The project will integrate community resources into the patient-centered medical home model of Group Health, a nonprofit healthcare system that provides coverage and care. The project will enhance patient resources and options for managing and preventing chronic illness and improve patient-centered outcomes. The project's specific aims are: * Aim 1: Develop, implement, and evaluate new methods to involve patients intensively in care design. The investigators will create processes and tools to select and train participants and facilitate their productive contributions to care design. The investigators will document the approach's benefits and challenges using qualitative and quantitative data. * Aim 2: Design and pilot a new CRS role for primary care teams. Robust engagement of patients in designing this new primary care team role will result in innovative, patient-centered solutions. The investigators will pilot this service at three clinics. The aim of the new service is to help patients more readily access the healthcare and community resources they need for preventing and treating chronic disease. The CRS also may help educate clinic staff about available community resources and increase the primary care team's use of holistic approaches to health. * Aim 3: Evaluate the design and efficacy of the CRS. The investigators will conduct both formative and outcome evaluations of the CRS role.
Interventions
CRS will work with patients to create goals, develop action plans and link to community resources to support goals
Sponsors
Study design
Eligibility
Inclusion criteria
* Enrolled at Group Health Cooperative, Seattle, Washington, in one of three pilot primary care clinics * Referred or self-referred to the CRS for connection to community resources to support health goals
Exclusion criteria
* Not enrolled at Group Health * Not enrolled in one of the pilot clinics
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Receiving a Resource for Community Services | 3 months | Number of patients who completed at least one visit with the CRS and were given a referral for at least one resource, service, or organization. This was assessed by abstraction and coding of CRS documentation in the medical record. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants Setting a Goal With Their CRS | 3 months | Number of patients who completed at least one visit with the CRS and set a specific action-based goal with their CRS. Patients could meet with the CRS and receive referrals to resources without setting specific action-based goals. This was assessed by abstraction and coding of CRS documentation in the medical record. |
Participant flow
Recruitment details
Enrollment period was 15 months, from July 2014 - December 2015.
Pre-assignment details
This was a single group observational study. All patients were considered enrolled who received care at one of 3 pilot clinics and were referred or self-referred to receive services from the Community Resource Specialist (CRS). They were considered complete if after referral they completed at least 1 phone or in-person CRS visit.
Participants by arm
| Arm | Count |
|---|---|
| Patients Presenting to Community Resource Specialist (CRS) Primary care patients who are referred or self-refer to the CRS for education and linkage to community resources that can help support health goals | 418 |
| Total | 418 |
Withdrawals & dropouts
| Period | Reason | FG000 |
|---|---|---|
| Overall Study | Referred: CRS unable to make contact | 62 |
| Overall Study | Referred: Declined service | 38 |
| Overall Study | Referred: unable to reach/resource sent | 104 |
Baseline characteristics
| Characteristic | Patients Presenting to Community Resource Specialist (CRS) |
|---|---|
| Age, Customized 19 - 34 | 38 participants |
| Age, Customized 35 - 64 | 165 participants |
| Age, Customized 65 or older | 145 participants |
| Age, Customized Less than or equal to 18 | 70 participants |
| Race/Ethnicity, Customized American Indian or Alaska Native | 12 participants |
| Race/Ethnicity, Customized Asian | 49 participants |
| Race/Ethnicity, Customized Black or African American | 83 participants |
| Race/Ethnicity, Customized Native Hawaiian or Other Pacific Islander | 11 participants |
| Race/Ethnicity, Customized Other | 20 participants |
| Race/Ethnicity, Customized Unknown | 15 participants |
| Race/Ethnicity, Customized White | 228 participants |
| Sex: Female, Male Female | 305 Participants |
| Sex: Female, Male Male | 113 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 0 / 418 |
| serious Total, serious adverse events | 0 / 418 |
Outcome results
Number of Participants Receiving a Resource for Community Services
Number of patients who completed at least one visit with the CRS and were given a referral for at least one resource, service, or organization. This was assessed by abstraction and coding of CRS documentation in the medical record.
Time frame: 3 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Patients Presenting to Community Liaison | Number of Participants Receiving a Resource for Community Services | 356 participants |
Number of Participants Setting a Goal With Their CRS
Number of patients who completed at least one visit with the CRS and set a specific action-based goal with their CRS. Patients could meet with the CRS and receive referrals to resources without setting specific action-based goals. This was assessed by abstraction and coding of CRS documentation in the medical record.
Time frame: 3 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Patients Presenting to Community Liaison | Number of Participants Setting a Goal With Their CRS | 162 participants |