Despite knowledge regarding the importance of controlling patients' blood pressure (BP) only 30% of treated patients achieve BP goals. Our objective was to determine the effect of frequent self measurements of BP in the patients' natural environment as a mean to improve BP control. Our hypothesis was that frequent measurements of BP will reduce mean BP levels...
Date First Received: April 10, 2007
Last Updated: April 10, 2007
Verified by: Sheba Medical Center, April 2007
Clinical Trial Phase: Phase 3 | Start Date: December 2002
Overall Status: Completed
Estimated Enrollment: 150
Brief Summary
Official Title: “The Effect of Frequent Self Measurements of Blood Pressure on the Control of Hypertension”
Condition Keyword(s):
Intervention(s):
Despite knowledge regarding the importance of controlling patients' blood pressure (BP) only 30% of treated patients achieve BP goals. Our objective was to determine the effect of frequent self measurements of BP in the patients' natural environment as a mean to improve BP control. Our hypothesis was that frequent measurements of BP will reduce mean BP levels.
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Intervention(s) in this Clinical Trial
- Device: Portable blood pressure wrist manometer
Outcome Measures for this Clinical Trial
Primary Measures
- Meam blood pressure
Secondary Measures
- Satisfaction
- Quality of life
Criteria for Participation in this Clinical Trial
Inclusion Criteria:
- Signing an informed consent form
- Having a diagnosis of hypertension for more than one year according to patients'records.
- receiving at least one medication for hypertension
- A reasonable understanding of Hebrew
- An ambulatory state enabling regular visits to a primary physician in the community and self-measurement of hypertension using the electronic device
Exclusion Criteria:
- Lack of willingness to participate in the study.Known arrhythmia
- Malignant disease
- Poor understanding of Hebrew
Gender Eligibility for this Clinical Trial: Both
Minimum Age for this Clinical Trial: 18 Years
Maximum Age for this Clinical Trial: N/A
Are Healthy Volunteers Accepted for this Clinical Trial?: No
Clinical Trial Sponsor Information
Lead Sponsor: Sheba Medical Center
Overall Clinical Trial Officials and Contacts
Yasmin Maor, MD Principal Investigator Sheba Medical Center
Additional Information
Information obtained from ClinicalTrials.gov on August 28, 2008
Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00459017
Study ID Number: SHEBA -02-2773-YM-CTIL
ClinicalTrials.gov Identifier: NCT00459017
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration
Clinical Trials Authorship and Review
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