Using an Electronic Personal Health Record to Empower Patients With Hypertension
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Purpose
Project Summary:
An electronic personal health record (ePHR) could maximize patient/clinician collaboration and consequently improve patient self-management and related health outcomes. The purpose of the proposed project is to examine the feasibility, acceptability, and impact of an ePHR that has been modified using a patient- and family-centered approach and incorporates the experiences, perspectives, and insights of patients and family members actually using the system. Comparison of patients with the ePHR intervention to a group of "care as usual" patients will be performed. The investigators Specific Aims are: (1) To improve the application of patient- and family-centered care elements in an existing ePHR, based on feedback from a pilot study of patients and their families. The modified ePHR will be tested in a pilot group of patients with hypertension and their families. (2) To implement and test the effectiveness of the modified ePHR with patients being treated for hypertension by a team of physicians, mid-level practitioners, nurse clinicians, and support staff in two ambulatory settings. Outcome measures will include patient activation and perception of care, quantifiable biological markers, patient-physician communication, and congruence of treatment with guidelines, particularly medication management; (3) To monitor the shift in provider and support staff awareness and incorporation of patient- and family-centered care as a result of implementation of the ePHR using questionnaires and focus groups. If successful, this ePHR could be implemented in additional locations in the Southeast.
| Condition | Intervention |
|---|---|
|
Hypertension |
Other: Electronic personal health record |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Factorial Assignment Masking: Single Blind (Investigator) |
| Official Title: | Using an Electronic Personal Health Record to Empower Patients With Hypertension |
- Systolic blood pressure [ Time Frame: 9 months ] [ Designated as safety issue: No ]2 seated measures taken using manual sphygmometer by trained research associate
- Diastolic blood pressure [ Time Frame: 9 months ]2 seated measures taken using manual sphygmometer by trained research associate
- patient activation [ Time Frame: 9 months ] [ Designated as safety issue: No ]Patients complete the validated paper-and-pencil Patient Activation Measure (PAM) developed by Judy Hibbard. The instrument assesses the degree to which a patient is "activated," that is the degree to which they are an active agent in their own health care, e.g. ask questions of their health care provider.
- Patient satisfaction with care [ Time Frame: 9 months ] [ Designated as safety issue: No ]Consumer Assessment of Health care--group and clinician survey Patient assessment of chronic care Post study interviews
- adherence to guidelines [ Time Frame: 9 months ] [ Designated as safety issue: No ]chart audit of patient care
| Enrollment: | 445 |
| Study Start Date: | September 2007 |
| Study Completion Date: | July 2010 |
| Primary Completion Date: | July 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Received personal health record
received personal health record access
|
Other: Electronic personal health record |
|
No Intervention: No personal health record
did not receive personal health record
|
Eligibility| Ages Eligible for Study: | 21 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- age 21
- hypertension
- referral by physician
Exclusion Criteria:
- age over 80
- no hypertension
- too ill to participate
Contacts and Locations| United States, Georgia | |
| Georgia Health Sciences University | |
| Augusta, Georgia, United States, 30912 | |
| Principal Investigator: | Peggy J Wagner, PhD | Georgia Regents University |
More Information
No publications provided by Georgia Regents University
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Peggy J Wagner, Georgia Health Sciences University |
| ClinicalTrials.gov Identifier: | NCT01317537 History of Changes |
| Other Study ID Numbers: | HS017234 |
| Study First Received: | March 2, 2011 |
| Last Updated: | March 16, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Georgia Regents University:
|
personal health records |
Additional relevant MeSH terms:
|
Hypertension Vascular Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on June 18, 2013