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A Study in the Use of Home Blood Pressure Monitoring and Telephone Follow-up to Control Blood Pressure

A Structured Program for Hypertension Control in Community Clinics: A Randomized Trial

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00662753
Enrollment
111
Registered
2008-04-21
Start date
2008-04-30
Completion date
2015-06-30
Last updated
2016-02-25

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

Conditions

Hypertension

Keywords

hypertension, home blood pressure monitoring, nurse telephone follow up, medically underserved populations

Brief summary

The purpose of this study is to determine if the use of home blood pressure monitors plus nurse telephone monitoring is more effective than the use of blood pressure monitors alone in improving control of high blood pressure in an urban medical clinic.

Detailed description

Participants will all have home blood pressure monitors, education session on controlling their blood pressure and will be randomized to recieve 6 months of intensive telephonic on a set monitoring schedule or no telephonic follow up. Phone calls will be weekly for 4 weeks, then every 2 weeks for 8 weeks then monthly for 3 months.

Interventions

Participants will receive a home blood pressure monitor and be taught how to use it. They will have an education session to review treatment goals, medications, diet and exercise. They will be asked to see their primary care provider at least every 3 months and the research nurse at 3, 6 and 12 months.

OTHERmonitor & phone call

Participants will receive all of the same interventions of the home monitoring group plus they will receive scheduled telephone follow up by the research nurse

Sponsors

George Washington University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* diagnosed with essential hypertension * systolic blood pressure \>140 mm Hg (130 if diabetic) OR diastolic blood pressure \> 90 mm Hg (80 if diabetic)on at least 2 clinic visits prior to randomization * BP at time of screening is \> than systolic 140 (130 if diabetic) or diastolic 90 (80 if diabetic) * patient is prescribed at least 1 antihypertensive medication * Patient is fluent in English * Patient is easily accessible by telephone

Exclusion criteria

* persons with stage 4 or 5 chronic kidney disease or end stage renal disease on dialysis * Patients with a terminal illness * Patients with severe dementia or serious mental illness * Inability to preform self blood pressure monitoring * Patient lacks a functioning home phone or personal cellular phone * Pregnant or planning to get pregnant * Arm circumference exceeds the allowable limit on the largest home BP monitor cuff

Design outcomes

Primary

MeasureTime frame
Blood Pressureat 6 mo and 12 mo after randomization

Secondary

MeasureTime frame
Compliance with use of home blood pressure monitor6 and 12 months post randomization
Number and type of antihypertensives prescribed12 months post randomization
Patient satisfaction and Quality of Life6 and 12 months post randomization
Blood pressure measured at home6 and 12 months post randomization
Number of primary care provider visits12 months post randomization
Number and quality of adverse events3, 6, and 12 months post randomization
cost analysis12 months post randomization
Primary care provider satisfaction with intervention6 mo post randomization of a provider's first patient to enroll in the trial

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026