Clinical Trials Directory

Trials / Completed

CompletedNCT01787175

VA Integrated Medication Manager

Veterans Affairs Integrated Medication Manager

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
58 (actual)
Sponsor
University of Utah · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to advance the science of healthcare informatics and to improve medication management through the development of a new approach to the electronic medical record called the Integrated Medication Manager (IMM).

Detailed description

In an attempt to address problems patient non-compliance with quality goals barriers to access and integration of health information that impede achievement of treatment goals, the VA is developing a new approach to the electronic medical record. The VA is moving away from the paper-chart metaphor and towards an integrated representation of the patient's status and care process across time. One of the first steps in the development phase has been to explicitly relate patient conditions, therapies, and goals in the domain of pharmacotherapy. This is called Integrated Medication Management and draws on Hollnagel's Contextual Control Model. Providers will be able to plan care and create orders directly in the context of these explicit relationships. This application will be implemented nationwide through a web interface embedded within the existing Computerized Patient Record System (CPRS), the graphical user interface to VA Information Systems (VistA). Aim 1: Identify cognitive components of providers' therapeutic decision making in the field. Aim 2. Refine and evaluate the Integrated Medication Manager using simulation studies. * Aim 2.a. Refine interfaces and logic of the Integrated Medication Manager. * Aim 2.b. Compare the performance of the Integrated Medication Manager and usual CPRS. All hypotheses (below) test the use of IMM versus usual electronic medical record (EMR). * Speed of decision-making will be faster. * Accuracy of data interpretation (clinical assessment) will be higher. * Appropriateness of therapeutic plans will be higher. * Efficiency of gathering information will be higher. * Common ground measures will be higher. * Appropriateness of therapeutic plans will be higher when relevant data is outside the usual time horizon. * Appropriateness of therapeutic plans will be higher when complex associations among patient therapies and goals exist. * Appropriateness of therapeutic plans will be no lower when relevant data is not captured by the displays of the IMM. * Appropriateness of therapeutic plans will be higher when highly salient data is not germane to the most important problem. * Appropriateness of therapeutic plans will be higher when cognitive load is high due to interruptions.

Conditions

Interventions

TypeNameDescription
OTHERIntegrated Medication ManagerA theory based electronic health record. Half of the provider participants were assigned the IMM to use. The other half were assigned the VA's CPRS EHR to use for the simulation. Providers were randomly assigned to a EHR to use.

Timeline

Start date
2007-10-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2013-02-08
Last updated
2016-06-23
Results posted
2016-06-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01787175. Inclusion in this directory is not an endorsement.