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NCT01800201 · ClinicalTrials.gov registry record · NA
Automated Hovering to Improve Medication Adherence Among Myocardial Infarction Patients (Heartstrong)
A NA study of Patients With Principal or Secondary Diagnosis Code of Intrntl Classification of Diseases, 9th Revision, (ICD-9-CM) 410 (Except When 5th Digit Was 2), sponsored by University of Pennsylvania.
- Completed
- Registry status
- NA
- Development phase
- 1,509
- Enrollment target
- 1
- Study location
NCT01800201 is a NA study of Patients With Principal or Secondary Diagnosis Code of Intrntl Classification of Diseases, 9th Revision, (ICD-9-CM) 410 (Except When 5th Digit Was 2) that has completed, run by University of Pennsylvania. The registered enrollment target is 1,509 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01800201, a NA study of Patients With Principal or Secondary Diagnosis Code of Intrntl Classification of Diseases, 9th Revision, (ICD-9-CM) 410 (Except When 5th Digit Was 2), has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,509 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this proposal is to test the implementation of an innovative approach to improving health and lowering cost for a high risk population of patients with acute myocardial infarction (AMI) immediately post-hospitalization. The investigators will implement a new service delivery approach that will provide a foundation for a payment system that rewards keeping high-risk patients healthy and that deploys technology and a health care workforce of the future to implement prevention, care coordination, care process re-engineering, team-based care, and the use of data to support new care delivery models. This program is focused on coronary artery disease (CAD), but we expect that a successful implementation of this model will demonstrate a sustainable pathway to the three-part aim not just for CAD, but for many other conditions whose outcomes are highly sensitive to post-discharge coordination. This proposal has three main principles: 1. Principles of behavioral economics that have been developed, refined, and tested over the past decade offer practical insights into health behaviors that were previously unavailable and are not reflected in existing care models. 2. New technology, typically wireless devices for pill bottles, and mobile telephones, make engagement with patients substantially easier and more immediate now than ever before. 3. While randomized clinical intervention trials provide exceptional confidence of comparative effectiveness in narrow interventions, they are slow and rigid and dont reflect the urgency that health care transformation currently requires. Principles of rapid cycle innovation are gaining acceptance as an alternative to or supplement of these traditional methods in supporting evidence for implementation success.
Conditions Studied
Interventions
- BEHAVIORAL Electronic Pill Bottle, Incentives, Social Influence
Study Locations (1)
Pennsylvania
- University of Pennsylvania - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,509 participants |
| Start Date | 2013-03 |
| Est. Completion | 2017-06 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01800201
The ClinicalTrials.gov registry entry for NCT01800201 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,509 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Patients With Principal or Secondary Diagnosis Code of Intrntl Classification of Diseases, 9th Revision, (ICD-9-CM) 410 (Except When 5th Digit Was 2) appearing as the primary indexed condition, and to 1 intervention - of which Electronic Pill Bottle, Incentives, Social Influence is the first listed.
NCT01800201 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01800201 about?
NCT01800201 is a clinical study titled "Automated Hovering to Improve Medication Adherence Among Myocardial Infarction Patients (Heartstrong)". The goal of this proposal is to test the implementation of an innovative approach to improving health and lowering cost for a high risk population of patients with acute myocardial infarction (AMI) immediately post-hospitalization. The investigators will implement a new service delivery approach tha...
What is the current status of trial NCT01800201?
This trial is currently completed. It is a NA study. The enrollment target is 1,509 participants. The study started on 2013-03. Estimated completion is 2017-06.
What conditions does trial NCT01800201 study?
This clinical trial studies the following conditions: Patients With Principal or Secondary Diagnosis Code of Intrntl Classification of Diseases, 9th Revision, (ICD-9-CM) 410 (Except When 5th Digit Was 2).
What interventions are being tested in trial NCT01800201?
The interventions under investigation include: Electronic Pill Bottle, Incentives, Social Influence (BEHAVIORAL).
Who is sponsoring clinical trial NCT01800201?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01800201 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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