A Randomized Controlled Trial of a Novel Community-based Primary and Secondary Cardiovascular Prevention Program

NCT00236210 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 422

Last updated 2009-08-04

No results posted yet for this study

Summary

VIP is a demonstration project with a goal to decrease modifiable risk factors for those with a higher risk of having a vascular event such as a heart attack or stroke or of developing vascular disease. Introduced as a study, VIP compares whether there is a significant reduction of modifiable vascular risk factors among patients who are involved in a personalized directed program versus those being provided standard care by their physician. Health care providers work collaboratively with the 'VIP Team' to improve the participants' vascular health.

Conditions

Interventions

BEHAVIORAL

Action Score

Improvement in a novel 100-point score summarizing cardiovascular risk.

BEHAVIORAL

VIP program

Risk assessment, lifestyle counselling, exercise program

Sponsors & Collaborators

  • Ontario Ministry of Health and Long Term Care

    collaborator OTHER_GOV
  • McMaster University

    collaborator OTHER
  • Coalition for the Acquisition of Sound Habits

    collaborator OTHER
  • Ministry of Northern Development and Mines Youth Internship Program

    collaborator UNKNOWN
  • Pfizer

    collaborator INDUSTRY
  • Group Health Centre

    lead OTHER

Principal Investigators

  • David Crookston, MD CCFP · Algoma District Medical Group and Group Health Centre

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-08-31
Primary Completion
2006-07-31
Completion
2006-07-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00236210 on ClinicalTrials.gov