Virtual Health Record (VHR)
OtherTechnology 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.
NCT Number: NCT01147328
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.
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Notify Me18 year and older
All sexes
Observational
HealtheLink, Buffalo, New York, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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.
Time frame: 1 year
Data from the VHR web portal database which records patient consent and provider usage of the web portal
Time frame: 1 year
A retrospective set of claims data will be used to characterize healthcare utilization and describe the study population
Weill Medical College of Cornell University
Other
Acronym: VHR
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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