Using an Electronic Personal Health Record to Empower Patients With Hypertension
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Hypertension
- Sponsor
- Augusta University
- Enrollment
- 445
- Locations
- 1
- Primary Endpoint
- Systolic blood pressure
- Status
- Completed
- Last Updated
- 15 years ago
Overview
Brief Summary
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.
Investigators
Eligibility Criteria
Inclusion Criteria
- •hypertension
- •referral by physician
Exclusion Criteria
- •age over 80
- •no hypertension
- •too ill to participate
Outcomes
Primary Outcomes
Systolic blood pressure
Time Frame: 9 months
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
Secondary Outcomes
- patient activation(9 months)
- Patient satisfaction with care(9 months)
- adherence to guidelines(9 months)