- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01147328
Assessing the Impact of Health Information Exchange (HIE) on Healthcare Utilization (VHR)
August 17, 2018 updated by: Weill Medical College of Cornell University
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
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.
Study Type
Observational
Enrollment (Actual)
218766
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
Buffalo, New York, United States, 14225
- HealtheLink
-
New York, New York, United States, 10065
- Weill Medical College of Cornell University
-
Rochester, New York, United States, 14614
- Rochester RHIO
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adult patients with concurrent controls who have consented to have their clinical data viewed by their providers using the VHR portal provided by RHIOs.
Providers who are participating in the Regional Health Information Exchange (RHIO).
Description
Inclusion Criteria:
- Patients that are aged 18 and older who have consented during the year 2009 to allow their provider use of their VHR data and had at least one visit to a healthcare provider that is a VHR user within 6 months after they consented to allow their provider use of their VHR data. (Note: we only wish to include individuals who have had the opportunity for their data to be viewed using the VHR web portal). Providers who are participating in the Regional Health Information Exchange (RHIO).
Exclusion Criteria:
- Patients and providers who do not meet the above criteria
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
Patients who did not have their data accessed in the VHR by a provider within 6 months after they consented will be part of the control group
|
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.
|
2
Patients who had their data accessed in the VHR by a provider within 6 months after they consented will be part of the intervention group
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
VHR Usage
Time Frame: 1 year
|
Data from the VHR web portal database which records patient consent and provider usage of the web portal
|
1 year
|
Changes in Healthcare Utilization
Time Frame: 1 year
|
A retrospective set of claims data will be used to characterize healthcare utilization and describe the study population
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Chair: Lisa Kern, MD, MPH, Weill Medical College of Cornell University
- Study Chair: Yolanda Barron, MS, Weill Medical College of Cornell University
- Study Chair: Alison Edwards, MStat, Weill Medical College of Cornell University
- Study Chair: Ranjit Singh, MD, MA, MBA, Weill Medical College of Cornell University
- Study Chair: Renny Varghese, MPH, Weill Medical College of Cornell University
- Principal Investigator: Vaishali Patel, PhD, MPH, Weill Medical College of Cornell University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2011
Primary Completion (Actual)
August 1, 2016
Study Completion (Actual)
August 1, 2016
Study Registration Dates
First Submitted
June 16, 2010
First Submitted That Met QC Criteria
June 16, 2010
First Posted (Estimate)
June 22, 2010
Study Record Updates
Last Update Posted (Actual)
August 21, 2018
Last Update Submitted That Met QC Criteria
August 17, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 0708160258-08
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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