- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03919084
THRIVE+ Pharmacy Liaison-Patient Navigation Intervention (THRIVE+)
March 16, 2021 updated by: Boston Medical Center
A Pharmacy Liaison-Patient Navigation Intervention to Reduce Inpatient and Emergency Department Utilization Among Primary Care Patients in a Medicaid Accountable Care Organization: A Pragmatic Trial
This is a pragmatic comparative effectiveness trial (n=364) to compare two screening and referral program models to address health-related social needs (HRSN) among the intermediate risk population of Boston Accountable Care Organization (BACO), a Medicaid ACO.
The first study arm is THRIVE-Basic, the low-touch usual care model already implemented in all primary care clinics at Boston Medical Center (BMC) where patients are screened for HRSN and receive a printed paper resource referral guide.
The second study arm is THRIVE+, which enhances the THRIVE-Basic model by engaging a pharmacy liaison-patient navigator to provide targeted navigation services and motivational interviewing to ensure connection to hospital- and community-based resources.
The patient navigators will also interface directly with a partner community organization, Action for Boston Community Development (ABCD), to further help connect patients receiving THRIVE+ to community resources for HRSN.
All patients in our study will receive pharmacy services via an existing Pharmacy Care Program.
Patients in study arm 1 will be connected to a pharmacy liaison, which is standard clinical practice for intermediate risk ACO members in the BMC General Internal Medicine clinics.
Patients in study arm 2 will receive systematic screening for and addressing of HRSN (THRIVE+) via a pharmacy liaison-patient navigator (a pharmacy technician trained as a patient navigator to deploy both pharmacy services and the THRIVE+ intervention), thereby avoiding duplication of services and multiple touches.
Assignment to the study arms will be linked to existing Pharmacy Care Program enrollment activities and will be based on medical record number.
The investigators' rationale for the study is that if patients' HRSN are addressed, patients will be better positioned to manage chronic conditions, adhere to preventive care plans, and less likely to use the emergency department (a conduit to inpatient care) for ambulatory care-sensitive conditions.
The effectiveness of these two models will be compared with respect to alleviating HRSN and reducing acute health care utilization over a 12-month follow-up period.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
364
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02118
- Boston Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 64 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Identified as within the 3rd to 10th percentile for healthcare utilization and cost among Boston Accountable Care Organization (BACO) Medicaid ACO membership at the time of enrollment in the clinical program; and
- Attend a primary care visit with a primary care provider (PCP-nurse practitioner or physician) in General Internal Medicine at Boston University Medical Center.
Exclusion Criteria:
-Patients who are receiving services from the BACO complex care management program.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: THRIVE-Basic
Screening-and-referral usual care model
|
The THRIVE screening tool includes questions to identify eight potentially unmet health-related social needs associated with health outcomes and healthcare utilization: housing and food insecurity, inability to afford medications, need for transportation, trouble paying for heat and electricity, need for employment or education, and difficulty taking care of children or other family members.
The survey is written at a 3rd grade reading level, is available in multiple languages, and requires less than five minutes to complete.
The paper screener consists of two parts: part one screens patients for health-related social needs in the eight domains.
Part two asks patients to indicate the resources they want help accessing across the eight domains.
Patients who request resources in one or more domains receive paper guides that describe available hospital and community resources to address the specific domain(s) indicated.
Other Names:
Pharmacy services provided by a pharmacy liaison include assessing gaps in obtaining refills, identifying barriers to medication adherence, reviewing the patient's engagement in medical care, and developing an action plan with the patient.
Action plans focus on strategies to increase medication adherence and engagement in care.
The pharmacy liaison will also link the patient to a clinical pharmacist, when appropriate, and will assist the patient with prescription management.
After the initial intake is completed, the pharmacy liaison will call patients monthly (or meet with them prior to or following scheduled appointments) over a twelve-month period to confirm medication adherence and address any new barriers to medication adherence and engagement in medical care.
The pharmacy liaison in the control arm does not systematically initiate screening for health-related social needs.
|
|
Experimental: THRIVE+
Enhanced screening-and-referral with motivational interviewing and patient navigation services
|
The THRIVE screening tool includes questions to identify eight potentially unmet health-related social needs associated with health outcomes and healthcare utilization: housing and food insecurity, inability to afford medications, need for transportation, trouble paying for heat and electricity, need for employment or education, and difficulty taking care of children or other family members.
The survey is written at a 3rd grade reading level, is available in multiple languages, and requires less than five minutes to complete.
The paper screener consists of two parts: part one screens patients for health-related social needs in the eight domains.
Part two asks patients to indicate the resources they want help accessing across the eight domains.
Patients who request resources in one or more domains receive paper guides that describe available hospital and community resources to address the specific domain(s) indicated.
Other Names:
Pharmacy services provided by a pharmacy liaison include assessing gaps in obtaining refills, identifying barriers to medication adherence, reviewing the patient's engagement in medical care, and developing an action plan with the patient.
Action plans focus on strategies to increase medication adherence and engagement in care.
The pharmacy liaison will also link the patient to a clinical pharmacist, when appropriate, and will assist the patient with prescription management.
After the initial intake is completed, the pharmacy liaison will call patients monthly (or meet with them prior to or following scheduled appointments) over a twelve-month period to confirm medication adherence and address any new barriers to medication adherence and engagement in medical care.
The pharmacy liaison in the control arm does not systematically initiate screening for health-related social needs.
In traditional patient navigation programs, a lay person from the community guides individuals through the healthcare system to receive appropriate services.
For the present study, the research team will train pharmacy liaisons (pharmacy technicians or pharmacy interns with at least a high school degree and four years of pharmacy experience) to provide patient navigation services, in addition to providing medication adherence support and assistance resolving barriers to accessing medication.
In an effort to avoid duplication of services the patient navigation intervention will be delivered via a pharmacy liaison trained in patient navigation, thereby decreasing multiple intervention providers and increasing the potential for sustainability should the intervention prove effective.
Motivational interviewing is a counseling method that encourages patient-centered discussions.
Motivational interviewing will be delivered by the intervention arm pharmacy liaison-patient navigators to identify the patient's unmet needs and encourage the patient to adopt behavior change that will promote engagement with resources and services to mitigate or alleviate HRSN.
The pharmacy liaison-patient navigator will partner with a community organization, Action for Boston Community Development (ABCD).
ABCD will help connect patients receiving THRIVE+ to community resources including childcare, food, heating, and housing.
The pharmacy liaison-patient navigator will interface directly with ABCD to coordinate receipt of resources for their patients.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Acute healthcare utilization composite measure
Time Frame: 12 months
|
Measure includes all-cause hospital admissions and all-cause emergency department visits.
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of all-cause emergency department visits
Time Frame: 12 months
|
Total number of all-cause emergency department visits.
|
12 months
|
|
Number of 30-day emergency department revisits
Time Frame: 12 months
|
Total number of all-cause emergency department revisits within thirty (30) days of initial emergency department visit.
|
12 months
|
|
Emergency department revisits rate
Time Frame: 12 months
|
Total number of all-cause emergency department revisits within thirty (30) days of initial emergency department visit divided by total number of all-cause emergency department visits.
|
12 months
|
|
Number of all-cause hospital discharges
Time Frame: 12 months
|
Total number of all-cause discharges from inpatient status
|
12 months
|
|
Number of 30-day hospital readmissions
Time Frame: 12 months
|
Total number of all-cause discharges from inpatient status that had a subsequent admission within thirty (30) days of the initial discharge.
|
12 months
|
|
30-day inpatient readmission rate
Time Frame: 12 months
|
Total number of all-cause discharges from inpatient status that had a subsequent admission within thirty (30) days of the initial discharge divided by total number of all-cause discharges from inpatient status.
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Karen Lasser, MD MPH, Boston Medical Center
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 28, 2019
Primary Completion (Actual)
March 5, 2021
Study Completion (Actual)
March 5, 2021
Study Registration Dates
First Submitted
April 15, 2019
First Submitted That Met QC Criteria
April 15, 2019
First Posted (Actual)
April 18, 2019
Study Record Updates
Last Update Posted (Actual)
March 18, 2021
Last Update Submitted That Met QC Criteria
March 16, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-38000
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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