- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03885401
Enhanced Care Planning for Patients With Multiple Chronic Conditions
June 27, 2025 updated by: Virginia Commonwealth University
Enhanced Care Planning and Clinical-Community Linkages to Comprehensively Address the Basic Needs of Patients With Multiple Chronic Conditions
Patients with multiple chronic conditions (MCC) have a range of needs that extend beyond traditional medical care, including behavioral, mental health, and social needs.
While primary care does its best to address these needs, few practices can undertake a systematic approach without broader health system and coordinated community support.
Fortunately, communities and health systems are investing in new models of care to address these needs.
New tools are emerging that allow for enhanced care planning to identify and prioritize patients' needs based on their values, preferences, social, and clinical context.
Additionally, support systems to promote partnerships between patients and clinical and community care teams are emerging.
Building on work occurring as part of the Richmond Accountable Health Community, the investigators propose to (a) evaluate the implementation of an enhanced care planning approach, paired with community-clinical linkages support to address health behavior, mental health, and social needs; (b) determine within a randomized controlled trial the benefit of this approach compared to usual care; and (c) assess which person, family, community, and system contextual factors that influence MCC.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
The number of patients in the United States with multiple chronic conditions (MCC) is growing.
Many patients with poorly controlled MCC also have unhealthy behaviors, mental health challenges, and unmet social needs.
Medical management of MCC may have limited benefit if patients are struggling to address these basic life needs.
Health systems and communities increasingly recognize the need to address these issues and are experimenting with and investing in new models for connecting patients with needed services.
Yet primary care clinicians, whose regular contact with patients makes them more familiar with patients' needs, are often not included in these systems.
Responding to the Special Emphasis Notice NOT-HS-16-013, Optimizing Care for People Living with MCC through the Development of Enhanced Care Planning, the investigators propose a clinician-level randomized controlled trial to study how primary care clinicians can participate in these community and hospital solutions and whether doing so is effective in controlling MCC.
This study will build on the Centers for Medicare and Medicaid Services (CMS)-funded Accountable Health Community (AHC) in Richmond, Virginia.
Sixty clinicians in the Virginia Ambulatory Care Outcomes Research Network (ACORN) will be matched by age and sex and randomized to usual care (control condition) or enhanced care planning with clinical-community linkage support (intervention).
From the electronic health record (EHR), clinicians will identify all patients with MCC, including cardiovascular disease or risks, diabetes, obesity, or depression.
A baseline assessment will be mailed to 50 randomly selected patients; 10 respondents per clinician (600 patients total) with uncontrolled MCC will be randomly selected, with over-sampling of minorities.
The intervention includes two components.
First, an enhanced care planning tool called My Own Health Report (MOHR) will screen patients for health behavior, mental health, and social needs.
Clinical navigator support will help patients prioritize needs, create care plans based on preferences, and write a personal narrative to guide the care team.
Patients will update care plans quarterly.
Second, community-clinical linkage support will include community resource registries, personnel to span settings (clinical navigators, community health workers), and care team coordination tools (sharing MOHR content, secure messaging, and virtual visits).
The investigators will compare patient-level intervention and control outcomes to assess improvements in MCC outcomes (primary outcome) and self-reported PROMIS-29 measures (physical health, mental health, social wellbeing) six months and two years post-enrollment.
the investigators will also conduct a mixed-methods, multilevel assessment of person-, family-, community-, and system-level contextual influences on implementation and effectiveness.
Data sources will include EHR and MOHR data, chart reviews, patient surveys, field notes, and semi-structured interviews of patients, clinicians, and community stakeholders.
If effective, this study will help inform efforts by primary care clinicians to participate in the growing number of AHC-like systems as a strategy to better control MCC.
Study Type
Interventional
Enrollment (Actual)
457
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
-
-
Virginia
-
Richmond, Virginia, United States, 23219
- Virginia Commonwealth University
-
-
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 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Two or more chronic conditions
- At least one uncontrolled condition
- Completes baseline survey
Exclusion Criteria:
- Participating in Richmond Accountable Health Community study
- Clinician excludes patients
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: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Enhanced care planning
The intervention consists of two components - enhanced care planning and clinical-community linkages.
The enhanced care plan is created using MOHR (https://myownhealthreport.org).
MOHR screens patients for unhealthy behaviors, mental health needs, and social needs.
Patients identify the needs they would like to address and create a care plan, which they update quarterly.
A clinical navigator and community health worker (CHW) help patients address their care plans using clinical-community linkages, which has four components.
First, clinicians and clinical navigators have a resource registry identifying community programs and support - No Wrong Door (NWD) and https://navigator.aafp.org/.
Second, MOHR shares information (care plans, patient narrative, and patient progress) across clinical and community team members.
Third, MOHR supports messaging and video visits for team members and patients.
Finally, MOHR sends care team members quarterly patient progress updates.
|
The intervention includes (1) screening for unhealthy behaviors, mental health needs, and social needs, (2) creation of a care plan, (3) quarterly updates to the plan, (4) a clinical navigator and community health worker to support accomplishing the care plan, (5) registry of community resources and programs, and (6) messaging and video-visit system for team members.
|
|
No Intervention: Usual medical care
Clinicians randomized to the control condition will continue to provide "usual care."
This includes current non-systematic assessment of health behaviors, mental health needs, and social needs.
Neither clinicians nor patients will be eligible to receive CHW support or have access to NWD.
Clinicians may refer some control patients to community programs as part of their current usual care.
Control clinicians will be blinded as to which patients are included in the study.
At the end of the study, the investigators will share with control clinicians our lessons learned, access to MOHR, and lists of useful community resources.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Enhanced care plan creation (implementation outcome)
Time Frame: Within 6 months of enrollment
|
This outcome reports the percent of intervention patients who complete the creation of an enhanced care plan (numerator = intervention patients who create an enhanced care plan / denominator = all enrolled intervention patients).
|
Within 6 months of enrollment
|
|
Health behavior, mental health, and social needs
Time Frame: Within 6 months of enrollment
|
This outcome will measure the number of health behavior, mental health, and social needs that patients have who complete an enhanced care plan.
This is a frequency count of each specific need based on the health risk assessment output.
|
Within 6 months of enrollment
|
|
Referral to and connection to community resources (implementation outcome)
Time Frame: Over 2 years after enrollment
|
This outcome will measure which community resources intervention patients are referred to for assistance with addressing health behaviors, mental health, and social needs.
This is a frequency count of the number of intervention patients referred to each potential community resource.
|
Over 2 years after enrollment
|
|
Effectiveness - chronic condition control
Time Frame: 6 months after creating a care plan
|
Percent of patients with an uncontrolled chronic condition for intervention patients versus usual care
|
6 months after creating a care plan
|
|
Maintenance - chronic condition control
Time Frame: 2 years after creating a care plan
|
Percent of patients with an uncontrolled chronic condition for intervention patients versus usual care
|
2 years after creating a care plan
|
|
Effectiveness - quality of life: Patient Reported Outcomes Measurement Information System (PROMIS-29)
Time Frame: 6 months after creating a care plan
|
Pre-post change in eight Patient Reported Outcomes Measurement Information System (PROMIS-29) domains for intervention patients versus usual care.
Norm-based scores will be calculated for each domain on the PROMIS measures, so that a score of 50 represents the mean or average of the reference population.
A score of 60 means that the person is one standard deviation above the reference population.
Higher scores means that the patient is reporting greater symptoms.
Scores will be calculated using the Healthmeasures Scoring Service (http://www.healthmeasures.net/score-and-interpret/calculate-scores).
|
6 months after creating a care plan
|
|
Maintenance - quality of life: eight PROMIS-29 domains
Time Frame: 2 years after creating a care plan
|
Pre-post change in eight PROMIS-29 domains for intervention patients versus usual care
|
2 years after creating a care plan
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Alex H Krist, MD MPH, Virginia Commonwealth University
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)
September 20, 2020
Primary Completion (Actual)
January 13, 2025
Study Completion (Actual)
January 13, 2025
Study Registration Dates
First Submitted
March 9, 2019
First Submitted That Met QC Criteria
March 19, 2019
First Posted (Actual)
March 21, 2019
Study Record Updates
Last Update Posted (Actual)
July 2, 2025
Last Update Submitted That Met QC Criteria
June 27, 2025
Last Verified
June 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HM20015553
- 1R01HS026223-01A1 (U.S. AHRQ Grant/Contract)
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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