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Blood Pressure Self Management for Hypertension & Prehypertension Using an Internet Enabled, Automated Self Management Program

Blood Pressure Self Management for Hypertension & Prehypertension Using an Internet Enabled, Automated Self Management Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00786162
Enrollment
404
Registered
2008-11-06
Start date
2007-04-30
Completion date
2008-12-31
Last updated
2012-03-15

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

Conditions

Blood Pressure

Brief summary

The specific aim of the study is to assess the impact of an Internet-enabled, automated, self-management program on blood pressure control of employees of a large local company.

Detailed description

We propose to conduct a randomized controlled trial of an Internet-enabled, automated self-management program. The study will be carried out through six local sites (offices) of a large employer. 3 sites will be intervention sites and 3 will be control sites. Subjects enrolled from the intervention sites will receive a blood pressure meter and access to an Internet site where they can view their readings, read educational material regarding hypertension management and receive personalized tips and feedback. Subjects enrolled from the control sites will have access to a blood pressure monitor located at their workplace but will only be provided with basic written information about hypertension at the start of the trial and will receive no feedback. The trial will run for 6 months from the time of enrollment and the primary outcome measure will be a change in systolic blood pressure.

Interventions

OTHERInternet-enabled automated self-management program

An internet platform to display blood pressure readings and provide subjects with automated messages and educational information about hypertension management.

OTHERBP cuff at workplace

Provided BP cuff for communal use at the worksite

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Full-time employees of EMC * Aged 30 to 65 years at time of enrollment * Any of the following * A diagnosis of hypertension as defined by one of the following * Taking an antihypertensive medication * Being told at least twice by a physician or other health professional that the subject has high blood pressure† * A BP \> 140/90 detected at screening by the research team on 2 separate occasions. * A diagnosis of prehypertension as defined by a systolic BP between 120-139 or a diastolic BP between 80-89 detected at screening by the research team on 2 separate occasions * Access to the Internet at work and / or at home

Exclusion criteria

* Inability to self-monitor blood pressure due to musculoskeletal or cognitive impairment * Known secondary cause of hypertension e.g. renal artery stenosis, Cushing's disease.

Design outcomes

Primary

MeasureTime frame
Change in systolic blood pressure.6 months

Secondary

MeasureTime frame
Assess whether the intervention increases the motivation and self-efficacy of patients managing blood pressure. Assess patient satisfaction with the intervention. Assess the impact of the intervention on healthcare utilization and expenditure6 months

Countries

United States

Outcome results

None listed

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