- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02812303
Implementation of a Population Health Chronic Disease Management Program
Implementation of a Population Health Chronic Disease Management Program in a Primary Care Network
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Massachusetts
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Boston, Massachusetts, United States, 02114
- Massachusetts General Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Diabetes mellitus (type 1 or type 2), or cardiovascular disease (including coronary artery disease, peripheral vascular disease, and cerebrovascular disease), or hypertension
- Breast cancer: women 50-74 years of age
- Cervical cancer: women 21-64 years of age
- Colorectal cancer: men or women 52-75 years of age
Exclusion Criteria:
- Patients not connected with a specific network physician or practice
- Patients who switched between PHC and non-PHC practices during the follow-up period
- Breast: bilateral mastectomy
- Cervical: total hysterectomy Colorectal: total colectomy
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Population Health Coordinator Support
8 practices received the support of central population health coordinators (PHCs). PHCs utilized a population health management (PHM) information technology (IT) tool and performed administrative tasks including appointment scheduling, ordering overdue laboratory testing, chart reviews, and obtaining outside tests/labs. In addition, PHCs regularly met with physicians to review those patients who required clinical intervention to develop an action plan. The network did not have sufficient resources to implement a PHC in all of the 18 network practices. So PHCs were allocated by responses from the practice leader, baseline quality scores, size of the practice, nature of the practice (health center vs not), and location of the practice. These decisions were made in a way that sought to equitably distribute available PHC resources within the practice network as a way to get network buy-in and maximize the impact of the program, both for practices with and without PHCs. |
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No Population Health Coordinator Support
Ten practices without PHC support were provided training on how to use the PHM IT tool.
The staff in these practices remained primarily responsible for managing administrative tasks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Difference in differences in Low density lipoprotein (LDL) goal achievement over the follow-up period comparing PHC to non-PHC practices
Time Frame: 6 months
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Among patients with diabetes and cardiovascular disease
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6 months
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Difference in differences in Hemoglobin A1c (HbA1c) goal achievement over the follow-up period comparing PHC and non-PHC practices
Time Frame: 6 months
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Among patients with diabetes
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6 months
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Difference in differences in Blood pressure (BP) goal achievement over the follow-up period comparing PHC and non-PHC practices
Time Frame: 6 months
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Among patients with diabetes and hypertension
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6 months
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Difference in differences in proportion of patients completing breast cancer screening over the follow-up period comparing PHC and non-PHC practices
Time Frame: 6 months
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6 months
|
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Difference in differences in proportion of patients completing cervical cancer screening over the follow-up period comparing PHC and non-PHC practices
Time Frame: 6 months
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6 months
|
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Difference in differences in proportion of patients completing colorectal cancer screening over the follow-up period comparing PHC and non-PHC practices
Time Frame: 6 months
|
6 months
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2009P002079
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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