Viewing Study NCT00853619



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Last Modification Date: 2024-10-26 @ 10:02 AM
Study NCT ID: NCT00853619
Status: UNKNOWN
Last Update Posted: 2012-02-29
First Post: 2009-02-26

Brief Title: Clinical Decision Support Consortium
Sponsor: Brigham and Womens Hospital
Organization: Brigham and Womens Hospital

Study Overview

Official Title: Clinical Decision Support Consortium for AHRQ CDS Research
Status: UNKNOWN
Status Verified Date: 2012-02
Last Known Status: ENROLLING_BY_INVITATION
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CDSC
Brief Summary: The goal of the Clinical Decision Support CDS Consortium research study is to assess define demonstrate and evaluate best practices for knowledge management KM and CDS in healthcare information technology across multiple ambulatory care settings and electronic health records EHR technology platforms

There are seven specific research objectives focusing on two practical areas of implementation for clinical decision support services a healthcare maintenance and preventive care screening and b two chronic disease conditions Coronary Artery Disease CAD and Adult-onset Diabetes Mellitus AODM The research objectives are 1 Knowledge management lifecycle 2 Knowledge specification 3 Knowledge portal and repository 4 CDS knowledge content and public web services 5 CDS Dashboard 6Evaluation and 7 Dissemination
Detailed Description: Investigators and developers of electronic health records from both academe and industry have come together to form the Clinical Decision Support CDS Consortium Members of the CDS Consortium are intimately involved in creating and providing CDS tools and services in electronic health records used in both academic settings as well as community-based physician office practices These investigators share a common interest and goal of enhancing the wide-spread adoption of CDS tools and services to improve the delivery of healthcare both domestically and world-wide

Our approach to the project is iterative and cyclical we will begin with a survey of the knowledge management lifecycle and supporting infrastructure such as knowledge management systems terminology services and data standards at the participating clinical sites We will then work together to define best practices for translating knowledge into a multi-layered array of human readable knowledge artifacts and public web services At each point in this process we will conduct careful evaluation documenting lessons learned from each site The ultimate work products will fall into three main categories

First tangible actionable knowledge artifacts such as the shareable human-readable and computable forms of clinical practice guidelines CPGs under study public web-services for CDS demonstrations and a CDS Knowledge Portal and Repository to facilitate widespread adoption of these artifacts

Second detailed guidance and recommendations based on what we learn from our combined efforts for external parties such as the Certification Commission for Health Information Technology CCHIT the Health Information Technology Standards Panel HITSP and the clinical practice guideline developer community

Third a set of knowledge and best practices such as methods for the knowledge management lifecycle development of both human readable knowledge artifacts and machine-interpretable knowledge and management of decision-support related organizational change We will share this knowledge through a variety of channels such as presentations and academic papers

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None