Clinical Trials Directory

Trials / Completed

CompletedNCT01147328

Assessing the Impact of Health Information Exchange (HIE) on Healthcare Utilization

Status
Completed
Phase
Study type
Observational
Enrollment
218,766 (actual)
Sponsor
Weill Medical College of Cornell University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to assess usage of the virtual health record (VHR), and determine the effects of this technology on healthcare utilization.

Detailed description

National efforts are underway to support the implementation of technology that enables providers to electronically access and view community-wide clinical information for their patients, which has the potential to improve quality of care and reduce health care costs by providing timely and complete health information at the point of care. However, few empirical studies have been conducted to evaluate the economic effects of this technology. Along with other stakeholders, New York State is funding regional health information organizations (RHIOs) to deploy a virtual health record (VHR), which is technology that enables providers to electronically access community-wide clinical data for patients who have consented to have their clinical data accessed via a web portal. RHIOs bring together multiple stakeholders, including physician practices, hospitals, pharmacies, and laboratories, for the purpose of exchanging clinical information electronically across communities. The investigators will conduct a multi-RHIO retrospective pre-post, cohort study of adult patients who have consented to have their clinical data viewed by their providers using the VHR portal. Examining the effects of electronically accessing clinical data on healthcare utilization across multiple settings and communities can help inform the national health IT initiative that is underway and allow assessment of the economic value of these technologies.

Conditions

Interventions

TypeNameDescription
OTHERVirtual Health Record (VHR)Technology that enables providers to electronically access community-wide clinical data for patients who have consented to have their clinical data accessed via a web portal.

Timeline

Start date
2011-06-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2010-06-22
Last updated
2018-08-21

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01147328. Inclusion in this directory is not an endorsement.