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Creating a Clinic-Community Liaison Role in Primary Care: Engaging Patients and Community in Health Care Innovation

Creating a Clinic-Community Liaison Role in Primary Care: Engaging Patients and Community in Health Care Innovation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02286193
Acronym
LINCC
Enrollment
418
Registered
2014-11-07
Start date
2013-03-31
Completion date
2016-03-31
Last updated
2017-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Community Integration, Patient Engagement

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

BEHAVIORALPatient clinical encounters with Community Resource Specialist (CRS)

CRS will work with patients to create goals, develop action plans and link to community resources to support goals

Sponsors

Patient-Centered Outcomes Research Institute
CollaboratorOTHER
Kaiser Permanente
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

MeasureTime frameDescription
Number of Participants Receiving a Resource for Community Services3 monthsNumber 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

MeasureTime frameDescription
Number of Participants Setting a Goal With Their CRS3 monthsNumber 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

ArmCount
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
Total418

Withdrawals & dropouts

PeriodReasonFG000
Overall StudyReferred: CRS unable to make contact62
Overall StudyReferred: Declined service38
Overall StudyReferred: unable to reach/resource sent104

Baseline characteristics

CharacteristicPatients 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 typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 418
serious
Total, serious adverse events
0 / 418

Outcome results

Primary

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

ArmMeasureValue (NUMBER)
Patients Presenting to Community LiaisonNumber of Participants Receiving a Resource for Community Services356 participants
Secondary

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

ArmMeasureValue (NUMBER)
Patients Presenting to Community LiaisonNumber of Participants Setting a Goal With Their CRS162 participants

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026