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Using an Electronic Personal Health Record to Empower Patients With Hypertension

Using an Electronic Personal Health Record to Empower Patients With Hypertension

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01317537
Enrollment
445
Registered
2011-03-17
Start date
2007-09-30
Completion date
2010-07-31
Last updated
2011-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

personal health records

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.

Interventions

OTHERElectronic personal health record

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
Cerner Corporation
CollaboratorUNKNOWN
The Institute for Patient- and Family-Centered Care
CollaboratorOTHER
Augusta University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
21 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* age 21 * hypertension * referral by physician

Exclusion criteria

* age over 80 * no hypertension * too ill to participate

Design outcomes

Primary

MeasureTime frameDescription
Systolic blood pressure9 months2 seated measures taken using manual sphygmometer by trained research associate
Diastolic blood pressure9 months2 seated measures taken using manual sphygmometer by trained research associate

Secondary

MeasureTime frameDescription
patient activation9 monthsPatients 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 care9 monthsConsumer Assessment of Health care--group and clinician survey Patient assessment of chronic care Post study interviews
adherence to guidelines9 monthschart audit of patient care

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026