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NCT00694239 Clinical Trial

Risk Assessment and Treat Compliance in Hypertension Education Trial

Hypertension Clinical Trial

— RATCHET  

Official title:
Evaluation of the Effect of Cardiovascular Risk Assessment in Treatment Compliance in Hypertension

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00694239
Other study ID # R-07-053
Secondary ID 13014E
Status Completed
Phase N/A
First received June 6, 2008
Last updated June 29, 2011
Start date May 2007
Est. completion date March 2011

Study information
Verified date June 2011
Source Lawson Health Research Institute
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The RATCHET study assesses if patient knowledge of estimated cardiovascular risk at current and recommended target blood pressure levels improves compliance in the management of hypertension.

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date March 2011
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 84 Years
Eligibility Inclusion Criteria:

- Essential hypertension (new diagnosis or established diagnosis) meeting criteria for pharmacologic therapy as defined by current guidelines

Exclusion Criteria:

- Lack of written informed consent

- Previous myocardial infarction

- Previous stroke

- Congestive heart failure

- Stage 3 or greater chronic kidney disease

- Pregnancy

- Usage of medication bubble/blister package

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Behavioral:
• Knowledge of Cardiovascular Risk Assessment
Knowledge of Cardiovascular Risk Assessment and risk reduction at target BP, reviewed every 3-6 months.

Locations
Country Name City State
Canada University of Western Ontario London Ontario

Sponsors (3)
Lead Sponsor Collaborator
Lawson Health Research Institute The Physicians' Services Incorporated Foundation, University of Western Ontario, Canada

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Medication Compliance 1 year No
Secondary Patient perception of cardiovascular risk 1 year No
Secondary Pilot Feasibility Study 1 year No
Secondary Blood Pressure 1 year No
Secondary Cholesterol Level 1 year No
Secondary Framingham Risk Score (stroke and coronary artery disease) 1 year No
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