The Healthy Options Feasibility Study
The Effectiveness of CVD Risk Profiles When Used by Allied Health Care Providers (HCP) Within a "Groupe de Médecine de Famille": The Healthy Options Feasibility Study.
1 other identifier
interventional
50
1 country
1
Brief Summary
The investigators hypothesize that having health care providers other than physicians within a "Groupe de Médecine de Famille" conduct cardiovascular risk assessments and teach lifestyle interventions to primary prevention patients will increase the likelihood that patients will adopt and maintain healthy lifestyles. These objectives will be supported by providing subjects with a cardiovascular risk profile estimating the subject's risk of cardiovascular disease and teaching them how to use the resources related to lifestyle changes available on the www.myhealthcheckup.com Web site.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable obesity
Started Jun 2008
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2008
CompletedFirst Submitted
Initial submission to the registry
September 3, 2008
CompletedFirst Posted
Study publicly available on registry
September 4, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
October 1, 2009
CompletedJanuary 14, 2014
January 1, 2014
10 months
September 3, 2008
January 10, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Feasibility of using health care providers other than physicians within a GMF to conduct a CV risk assessment and intervention on primary prevention patients
10 months
Secondary Outcomes (4)
Patient's CV risk factors and overall CV risk
16 weeks
Subject's adherence with lifestyle changes and prescribed medications
16 weeks
Satisfaction of the nurse
10 months
Satisfaction of the patient
16 weeks
Study Arms (1)
A
EXPERIMENTALBehavioral
Interventions
Eligibility Criteria
You may qualify if:
- Male or female subjects 30-79 years of age without known cardiovascular disease but with one or more risk factors such as obesity, a sedentary lifestyle, dyslipidemia, hypertension, cigarette smoking, or diabetes
- Have provided informed consent
- Recent (past 6 months) fasting lipid profile results in the medical charts
You may not qualify if:
- Unable or unlikely to follow and/or complete study or evidence of uncooperative attitude
- Subject is not literate in either French or English
- Subject does not have easy and regular access to the Internet
- Exercise or weight loss are contra-indicated for medical reasons
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- McGill Universitylead
- Pfizercollaborator
Study Sites (1)
McGill Cardiovascular Health Improvement Program
Montreal, Quebec, H3Z 2A7, Canada
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Steven Grover, MD
McGill Cardiovascualr Health Improvement Program
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Medical Director McGill Comprehensive Health Improvement Program
Study Record Dates
First Submitted
September 3, 2008
First Posted
September 4, 2008
Study Start
June 1, 2008
Primary Completion
April 1, 2009
Study Completion
October 1, 2009
Last Updated
January 14, 2014
Record last verified: 2014-01