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Clinical Trials/NCT00263393
NCT00263393
Completed
Phase 4

Evaluation of a Primary Health Care Intervention for the Prevention of Cardiovascular Disease in Rural Andhra Pradesh

The George Institute1 site in 1 country3,712 target enrollmentDecember 2005

Overview

Phase
Phase 4
Intervention
ASA, Atenolol, hydrochlorothiazide, ACE inhibitor, Statin
Conditions
Myocardial Infarction
Sponsor
The George Institute
Enrollment
3712
Locations
1
Primary Endpoint
The proportion of high-risk individuals that have been assessed for cardiovascular risk
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

This study will evaluate the effectiveness of a novel cardiovascular disease prevention program designed for delivery through existing primary health care services in rural villages in Andhra Pradesh.

The primary aim is to increase the number of high-risk individuals in the population that are appropriately managed with proven, low-cost preventive interventions. The corresponding null hypothesis is therefore that the prevention program will result in no change in the proportion of high-risk individuals identified and treated in villages assigned to intervention compared with those villages assigned to control.

Detailed Description

STUDY TYPE This project is a community intervention study that will use a large-scale, cluster-randomised design to compare the management of individuals at high cardiovascular risk in villages assigned to receive the cardiovascular prevention program (intervention) and villages assigned to continue usual practices (control). The definition of high-risk for treatment is based on an established history of previous vascular disease -heart attack or stroke- known hypertension or systolic blood pressure \> 160mmHg, or the presence of other risk factors such as smoking, high blood pressure, obesity, older age and family history which combined would result in a very high level of risk. INTERVENTION PROGRAM TO BE EVALUATED The program to be evaluated comprises: (1) simple strategies designed to facilitate the opportunistic identification of high-risk individuals, (2) clinical algorithms for the implementation of proven preventive interventions based on World Health Organisation recommendations (3) a health promotion campaign designed to aid self-identification and self-referral of high-risk people and (4) simple, structured education programs to assist patients to comply with their treatment. DATA COLLECTION Data to be collected will comprise an interviewer administered questionnaire with demographic details, basic medical history, cardiovascular risk factors, previous cardiovascular disease and any current treatments. This will be followed by a brief physical examination including measurement of blood pressure, heart rate, weight, height, waist and hip circumferences. Urine will be tested using a dipstick in all and all will have a fasting blood glucose assay. Fasting venous blood samples will be collected for assay of cholesterol, glucose and creatinine from a sample of 1,000.

Registry
clinicaltrials.gov
Start Date
December 2005
End Date
June 2009
Last Updated
7 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr Rohina Joshi

Research Fellow

The George Institute

Eligibility Criteria

Inclusion Criteria

  • Age 30 years and above
  • Personal history of heart attack or stroke
  • Presence of other cardiovascular risk factors such as smoking, overweight, diabetes

Exclusion Criteria

  • Mental disability
  • Not living in the Study area

Arms & Interventions

Algorithm-based care

An algorithm based approach to increase the identification of high-risk individuals in the community through encouraging opportunistic screening, and to increase the use of appropriate evidence based prevention strategies.

Intervention: ASA, Atenolol, hydrochlorothiazide, ACE inhibitor, Statin

Health-promotion

The health promotion arm has been designed to increase knowledge of the causes of cardiovascular disease and enhance use of preventive behaviours in the general population

Intervention: Health Promotion

Outcomes

Primary Outcomes

The proportion of high-risk individuals that have been assessed for cardiovascular risk

Time Frame: 12 months after intevention

The proportion of individuals with correct knowledge about the effects of behavioural determinants of the risk of cardiovascular disease

Time Frame: 12 months from intervention

Secondary Outcomes

  • The proportion of high risk individuals treated with two or more of the recommended drug therapies(12 months)
  • The knowledge, attitudes and practices of the population about preventable conditions and actions taken to prevent non-communicable disease(12 months from intervention)
  • The risk factor levels of the population identified as high risk.(12 months)

Study Sites (1)

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