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Comparison of Two Programs to Improve Blood Pressure Treatment Adherence

NCT00123058 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 777

Last updated 2014-09-08

No results posted yet for this study

Summary

The purpose of this study is to improve adherence to blood pressure (BP) monitoring and medication compliance in individuals with high BP.

Conditions

Interventions

BEHAVIORAL

Nurse administered

Subjects received a nurse administered behavioral intervention via telephone every 8 weeks for 24 months.

DEVICE

BP Monitor

Subjects received a study provided home BP monitor and recorded home BP 3 times per week for 24 months.

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    collaborator NIH

  • Pfizer

    collaborator INDUSTRY

  • Duke University

    lead OTHER

Principal Investigators

  • Hayden B. Bosworth · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-06-30
Primary Completion
2005-12-31
Completion
2007-06-30

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00123058 on ClinicalTrials.gov