Mechanisms and Therapeutic Effects of the Relaxation Response in Elderly Hypertensive Patients
NCT ID: NCT00179543
Last Updated: 2006-09-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
122 participants
INTERVENTIONAL
2001-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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Relaxation response
Eligibility Criteria
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Inclusion Criteria
* currently taking at least 2 anti-hypertensive medications
* systolic blood pressure between 140-159 mmHg
* diastolic blood pressure less than 90 mmHg
* read and understand English
* access to a telephone
* ability to attend all study visits
Exclusion Criteria
* major medical illness
* previous experience with any RR eliciting technique
* current use of:beta-agonist bronchodilators, systemic corticosteroids, anti-convulsants/psychotics, immunosuppressants, cytotoxic therapy, anabolic steroids, antidepressants (other than SSRIs), dicyclomine, bile acid binding resins, or sympathomimetic medication
55 Years
ALL
No
Sponsors
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Centers for Disease Control and Prevention
FED
Beth Israel Deaconess Medical Center
OTHER
Principal Investigators
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Herbert Benson, MD
Role: PRINCIPAL_INVESTIGATOR
Beth Israel Deaconess Medical Center
Locations
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BIDMC
Boston, Massachusetts, United States
Countries
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Other Identifiers
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CDC grant: H75-CCH-123424
Identifier Type: -
Identifier Source: secondary_id
CDC grant: H75-CCH-119124
Identifier Type: -
Identifier Source: secondary_id
CDC grant: R01 DP00039
Identifier Type: -
Identifier Source: secondary_id
2001-P-001727
Identifier Type: -
Identifier Source: org_study_id