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Does Access to an EHR Patient Portal Influence Chronic Disease Outcomes?
This study is currently recruiting participants.
Verified by Robert Wood Johnson Foundation, September 2006
Sponsors and Collaborators: Robert Wood Johnson Foundation
New York University School of Medicine
Information provided by: Robert Wood Johnson Foundation
ClinicalTrials.gov Identifier: NCT00147706
  Purpose

The purpose of this study is to determine if patients with congestive heart failure, diabetes or secondary cardiovascular diseases, who access HealthMedia's online tailored behavior change programs on the electronic health record patient portal have better clinical and behavioral change outcomes.


Condition Intervention
Congestive Heart Failure
Diabetes
Cardiovascular Disease
Procedure: Tailored Healthmedia programs on EHR Patient Portal

MedlinePlus related topics: Coping with Chronic Illness Diabetes Heart Failure
U.S. FDA Resources
Study Type: Interventional
Study Design: Educational/Counseling/Training, Randomized, Single Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: Does Access to an EHR Patient Portal Influence Chronic Disease Outcomes? A Randomised Trial Assessing Clinical and Behavioural Change Outcomes in Patients With CHF, Diabetes, or Secondary CVD

Further study details as provided by Robert Wood Johnson Foundation:

Primary Outcome Measures:
  • knowledge, behavior change, relevant clinical measures

Estimated Enrollment: 6000
Study Start Date: September 2004
Estimated Study Completion Date: February 2007
Detailed Description:

The specific aims of the study are to determine if e-portal interventions influence:

  • Measures of patient activation, patient self-management, treatment adherence, patient satisfaction with care, and disease specific knowledge.
  • Process measures relevant to appropriate care for CVD, CHF, and DM.
  • Clinical markers of cardiovascular or diabetes morbidity and risk.

These aims will be evaluated in one-year prospective study. Patients who use the portal will be randomized to control (i.e., access to routine portal-related information) and intervention groups (i.e., targeted and periodic messages designed to capture data relevant to self-management; to improve knowledge of their specific disease, tests, and risks; to devise time-dependent goals; and to motivate self-efficacy). Outcomes including activation, satisfaction, and adherence will be measured by telephone interview prior to and one year after intervention, and by lab and clinical measures and data available from the EHR. We will also evaluate potential selection issues among those who sign on to the e-portal by administering the same baseline interview to a matched (by disease and by age) random sample of patients who do not sign on to the e-portal.

Patients with chronic diseases are likely to experience particular benefit from online e-health resources as they have greater information needs and participate in self-management.(Camer, 2000) Unlike traditional office visits, online interactions eliminate the need to travel, are always available and give the patient access to a broad range of information, helping them actively participate in their own care.(Brown, 1999) There is growing evidence that patient education and engagement using e-health applications results in improved patient outcomes in the care of chronic illnesses, improved patient-physician communication, and reduction of anxiety for caregivers.(Brennan et al., 2001; Bronson et al., 1986; Bronson & O'Meara, 1986; Ross et al., 2003a, 2003b) We anticipate demonstrating clinically meaningful improvements in chronic disease health status, using evidence-based science delivered in behaviorally-validated ways.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adult age 18 years or older
  • Have medical records in the Geisinger Electronic Health Record
  • Have congestive heart failure and/or Diabetes and/or cardiovascular disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00147706

Contacts
Contact: Walter F Stewart, PhD 570-214-9391 wfstewart@geisinger.edu
Contact: Zahra S Daar, MS 570-214-9621 zsdaar@geisinger.edu

Locations
United States, Pennsylvania
Center for Health Research & Rural Advocacy. Geisinger Clinic Recruiting
Danville, Pennsylvania, United States, 17822-2602
Contact: Walter F Stewart, PhD     570-214-9391     wfstewart@geisinger.edu    
Contact: Zahra S Daar, MS     570-214-9621     zsdaar@geisinger.edu    
Principal Investigator: Walter F Stewart, PhD            
Sub-Investigator: Nirav R Shah, MD. MPH            
Sponsors and Collaborators
Robert Wood Johnson Foundation
New York University School of Medicine
Investigators
Principal Investigator: Walter F Stewart, PhD Geisinger Health Systems
Study Chair: Nirav R Shah, MD. MPH New York University School of Medicine
  More Information

Study ID Numbers: 051761
Study First Received: September 2, 2005
Last Updated: September 6, 2006
ClinicalTrials.gov Identifier: NCT00147706  
Health Authority: United States: Institutional Review Board

Keywords provided by Robert Wood Johnson Foundation:
Electronic Health Record
Patient Portal
Chronic Diseases

Study placed in the following topic categories:
Heart Failure
Heart Diseases
Diabetes Mellitus
Neoplasm Metastasis
Chronic Disease

Additional relevant MeSH terms:
Disease Attributes
Pathologic Processes
Cardiovascular Diseases

ClinicalTrials.gov processed this record on January 16, 2009