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OpenTrials
Completed

NCT Number: NCT01317537

Using an Electronic Personal Health Record to Empower Patients With Hypertension

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.

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Georgia Health Sciences University

Augusta, Georgia, 30912, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age 21
  • hypertension
  • referral by physician

Exclusion criteria

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

Treatment and study plan

Electronic personal health record

Other

Primary outcomes

  1. Systolic blood pressure

    Time frame: 9 months

    2 seated measures taken using manual sphygmometer by trained research associate

  2. Diastolic blood pressure

    Time frame: 9 months

    2 seated measures taken using manual sphygmometer by trained research associate

Secondary outcomes

  1. patient activation

    Time frame: 9 months

    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.

  2. Patient satisfaction with care

    Time frame: 9 months

    Consumer Assessment of Health care--group and clinician survey Patient assessment of chronic care Post study interviews

  3. adherence to guidelines

    Time frame: 9 months

    chart audit of patient care

Sponsors and collaborators

Lead sponsor

Augusta University

Other

Collaborators

  • Agency for Healthcare Research and Quality (AHRQ)
  • Cerner Corporation
  • The Institute for Patient- and Family-Centered Care

Registry information

Important dates

Study start
2007
Primary completion
2010
Study completion
2010
First posted
Mar 17, 2011
Registry last updated
Mar 17, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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