Home Blood Pressure Monitoring Project

Not Applicable

Completed

• Conditions: Hypertension
• Interventions: Behavioral: Home Blood Pressure Monitoring

• Registration Number: NCT01162759
• Lead Sponsor: Kaiser Permanente

Brief Summary

The goal of this project is to improve hypertension control at Kaiser Permanente Colorado (KPCO) by implementing a population-based multi-factorial intervention that uses home BP monitors that can download BP readings to KPCO's health records via internet, interactive voice response (IVR) technology, and multidisciplinary care team. Participants will be randomized to either the home blood pressure monitoring group receiving the multi-factorial intervention or the usual care group who will be receiving Kaiser standard of care. We will determine the proportion of patients in each group who achieve their target BP goals at 6 months, according to national clinical practice guidelines. The study hypothesis is that a higher proportion of patients with uncontrolled hypertension in the home blood pressure monitoring (HBPM) group will achieve their target blood pressure compared to those in the usual care (UC) group.

Detailed Description

STUDY OBJECTIVES:

Primary:

• To determine the proportion of patients in each group who achieve their target BP goals at 6 months, according to national clinical practice guidelines

Secondary:

The following parameters will be evaluated between groups:

* Change in BP measures between baseline and at 6 months

* Proportion of patients who are receiving antihypertensive treatments in accordance to national clinical practice guidelines

* Adherence to hypertensive medication regimen during the 6-month follow-up period

* Patient satisfaction with the care model.

Study Timeline

• Study Start: 2008-07
• Primary Completion: 2010-07
• Study Completion: 2010-07
• Study First Submitted: 2010-07-13
• Study First Submitted QC: 2010-07-13
• Study First Posted: 2010-07-15
• Status Verified: 2012-04
• Last Update Submitted: 2012-04-04
• Last Update Posted: 2012-04-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 348

Inclusion Criteria

• Age 18 to 85 years At least 1 diagnosis for hypertension,

  • Receive primary care from one of the participating clinics,
  • The two most recent BPs documented within that last 24 months are elevated (SBP>140 and/or DBP>90)
  • Receiving < 3 antihypertensive medications, and
  • Have access to a computer with a USB port.

Exclusion Criteria

• Pregnant, or breast-feeding,
• Patients on dialysis or being followed by nephrology,
• Patients with coronary artery disease, given these patients are already followed by the Clinical Pharmacy Cardiac Risk Service (CPCRS),
• On KPCO "Do Not Call" or deceased list,
• PCP does not give permission to include patient in the study,
• BP is at or below target at the baseline study visit,
• Not English-speaking.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Home Blood Pressure Monitoring Group	Home Blood Pressure Monitoring	Intervention group

Primary Outcome Measures

Name	Time	Method
BP at 6 months	6 months

Trial Locations

Locations (1)

Kaiser Permanente Colorado, Institute of Health Research; 🇺🇸 Denver, Colorado, United States