Evaluating the Effects of EHRs, P4P and Medical Home Redesign in the Hudson Valley
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT00793065 |
Recruitment Status :
Completed
First Posted : November 19, 2008
Last Update Posted : February 23, 2017
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment |
---|---|
Quality of Health Care Electronic Health Records | Other: Electronic health record (EHR) Other: Medical Home redesign |
Study Type : | Observational |
Actual Enrollment : | 438 participants |
Observational Model: | Cohort |
Time Perspective: | Prospective |
Official Title: | Evaluating the Effects of EHRs, P4P and Medical Home Redesign in the Hudson Valley |
Actual Study Start Date : | January 2008 |
Actual Primary Completion Date : | December 2012 |
Actual Study Completion Date : | December 2012 |
Group/Cohort | Intervention/treatment |
---|---|
1
Physicians that are using paper-based medical charts and who are not receiving Medical Home redesign incentives.
|
|
2
Physicians that are using Electronic Health Records (EHRs) and who are not undergoing Medical Home redesign.
|
Other: Electronic health record (EHR)
Computer-based system that allows physicians to access and manage patient records electronically. |
3
Physicians that are using Electronic Health Records (EHRs) and undergoing Medical Home redesign.
|
Other: Electronic health record (EHR)
Computer-based system that allows physicians to access and manage patient records electronically. Other: Medical Home redesign Implementation of NCQA Level III Medical Home |
- health care quality (as determined by previously selected and approved quality indicators) [ Time Frame: 5 years ]
- health care utilization [ Time Frame: 5 years ]

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Primary care physicians working in the offices practices in the Hudson Valley, and who are members of the Taconic IPA.
Exclusion Criteria:
- Physicians who opt out from the study.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00793065
United States, New York | |
Weill Cornell Medical College | |
New York, New York, United States, 10021 |
Principal Investigator: | Lisa M Kern, MD, MPH | Weill Medical College of Cornell University | |
Principal Investigator: | Rainu Kaushal, MD, MPH | Weill Medical College of Cornell University |
Responsible Party: | Weill Medical College of Cornell University |
ClinicalTrials.gov Identifier: | NCT00793065 |
Other Study ID Numbers: |
0508190240 |
First Posted: | November 19, 2008 Key Record Dates |
Last Update Posted: | February 23, 2017 |
Last Verified: | February 2017 |
electronic health records health information technology physician incentives quality of health care |