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Family Heart Health Program: Randomized, Controlled Trial (FHHP-RCT)

Primary Purpose

Coronary Heart Disease

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
12-week risk reduction program, managed by a Heart Health Educator
Sponsored by
Ottawa Heart Institute Research Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Coronary Heart Disease focused on measuring family risk, behavior modification, lifestyle change, prevention of CHD, health care costs

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Spouse, offspring or sibling of patient hospitalized at UOHI within the past 5 years for:

    1. Acute coronary syndrome (ACS);
    2. Elective percutaneous coronary intervention (PCI); or
    3. Bypass surgery (CABG);
  • Willing to provide informed consent;
  • At least one of the following modifiable risk factors:

    1. Current smoker;
    2. Systolic blood pressure ≥ 140 and or Diastolic BP ≥ 90 and/or currently on medication to treat high blood pressure;
    3. Total cholesterol/HDL-cholesterol ratio ≥ 5.0 and/or on antilipemic medication;
    4. Abdominal obesity (for men, waist circumference > 102 cm; for women, waist circumference > 88cm);
    5. Physical Inactivity [<150 min mod, 5-7 d/week or <100 min vig, 4-7 d/week]
  • Geographically available for assessment, intervention and follow-up.

Exclusion Criteria:

  1. Unable to understand English or French;
  2. History of diabetes mellitus or any atherosclerotic disease;
  3. Fasting glucose ≥ 7.0 mmol/L at screening;
  4. Presence of life threatening illness (e.g., known or suspected cancer or other disease with a life expectancy of less than five years);
  5. Chronic kidney disease and/or undergoing dialysis;
  6. Active liver disease;
  7. Pregnant or planning to become pregnant within the next year;
  8. Cognitive impairment;
  9. Other family member already participating in study.

Sites / Locations

  • University of Ottawa Heart Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

1

2

Arm Description

Family Heart Health Program

Usual Care

Outcomes

Primary Outcome Measures

TC/HDL ratio

Secondary Outcome Measures

Secondary outcomes of interest will include the modifiable components comprising the Framingham score (smoking status, systolic BP, total cholesterol, HDL- and LDL-cholesterol)
Use of risk reducing medications, use of health care resources, smoking status, leisure time exercise, dietary patterns, and body composition

Full Information

First Posted
November 1, 2007
Last Updated
February 24, 2022
Sponsor
Ottawa Heart Institute Research Corporation
Collaborators
Heart and Stroke Foundation of Canada
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1. Study Identification

Unique Protocol Identification Number
NCT00552591
Brief Title
Family Heart Health Program: Randomized, Controlled Trial
Acronym
FHHP-RCT
Official Title
Family Heart Health Program: Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Heart Institute Research Corporation
Collaborators
Heart and Stroke Foundation of Canada

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: Family members (spouses, siblings, offspring) of patients with coronary heart disease (CHD) may themselves be at increased risk for developing CHD for genetic, biochemical and/or behavioural reasons. Targeted approaches aimed at family members of those with established CHD may be a cost-effective way to identify high-risk persons and link them to effective risk factor modification. During pilot testing we found 29% of family members of patients recently hospitalized at our institution had ≥ 3 CHD risk factors. Encouragingly, they indicated high levels of "readiness" to change underlying risk behaviours such as cigarette smoking and physical inactivity. We have developed a 12-week family heart health program featuring a personal plan for achieving risk factor goals and weekly contact with a heart health educator. This intervention needs to be fully tested. Research Aims: In this study, we will: Compare the effects of a targeted family heart health (FHH) screening, counselling and follow-up program versus usual care (UC) for reducing participants total cholesterol/high density lipoprotein (TC/HDL) ratio 52 weeks after program entry, in family members of patients recently hospitalized with CHD; Compare the effects of the FHH program versus UC on modifiable components comprising the Framingham score, including: smoking status; systolic blood pressure; total cholesterol; and high density lipoprotein cholesterol; Compare the effects of the FHH program versus UC on: lifestyle-related factors (dietary patterns, leisure time exercise, body composition); medication use (anti-lipemic medications, anti-hypertensive medications, pharmacotherapies for smoking cessation); and use of healthcare resources (physician visits, hospitalization days, number of laboratory and diagnostic tests and procedures).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease
Keywords
family risk, behavior modification, lifestyle change, prevention of CHD, health care costs

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
426 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Family Heart Health Program
Arm Title
2
Arm Type
No Intervention
Arm Description
Usual Care
Intervention Type
Behavioral
Intervention Name(s)
12-week risk reduction program, managed by a Heart Health Educator
Intervention Description
The educator and participant will negotiate a personal plan for achieving the goals through lifestyle change (i.e. smoking cessation, increased exercise, improved nutrition) and, if necessary, pharmacotherapy coordinated by the participant's personal physician. Educational modules have been developed to address specific lifestyle issues including smoking cessation, healthy eating, exercise, and weight management, and will be provided to participants as required. A summary of the risk factor profile and personal plan will be incorporated into a report for the participant's personal physician as well. Participants will also receive telephone-based motivational counseling sessions for 12 weeks to address specific lifestyle issues.
Primary Outcome Measure Information:
Title
TC/HDL ratio
Time Frame
one year
Secondary Outcome Measure Information:
Title
Secondary outcomes of interest will include the modifiable components comprising the Framingham score (smoking status, systolic BP, total cholesterol, HDL- and LDL-cholesterol)
Time Frame
12 weeks and one year
Title
Use of risk reducing medications, use of health care resources, smoking status, leisure time exercise, dietary patterns, and body composition
Time Frame
12 weeks and one year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Spouse, offspring or sibling of patient hospitalized at UOHI within the past 5 years for: Acute coronary syndrome (ACS); Elective percutaneous coronary intervention (PCI); or Bypass surgery (CABG); Willing to provide informed consent; At least one of the following modifiable risk factors: Current smoker; Systolic blood pressure ≥ 140 and or Diastolic BP ≥ 90 and/or currently on medication to treat high blood pressure; Total cholesterol/HDL-cholesterol ratio ≥ 5.0 and/or on antilipemic medication; Abdominal obesity (for men, waist circumference > 102 cm; for women, waist circumference > 88cm); Physical Inactivity [<150 min mod, 5-7 d/week or <100 min vig, 4-7 d/week] Geographically available for assessment, intervention and follow-up. Exclusion Criteria: Unable to understand English or French; History of diabetes mellitus or any atherosclerotic disease; Fasting glucose ≥ 7.0 mmol/L at screening; Presence of life threatening illness (e.g., known or suspected cancer or other disease with a life expectancy of less than five years); Chronic kidney disease and/or undergoing dialysis; Active liver disease; Pregnant or planning to become pregnant within the next year; Cognitive impairment; Other family member already participating in study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert D Reid, MBA, PhD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Andrew L Pipe, MD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Lori J Mosca, MD, PhD
Organizational Affiliation
New York Presbyterian Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Heidi Mochari, MPH, RD
Organizational Affiliation
New York Presbyterian Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
George Wells, PhD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Louise J Beaton, MSc
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Pat O'Farrell, RN
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Chris M Blanchard, PhD
Organizational Affiliation
Dalhousie University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Sophia Papadakis, MHA
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Monika Slovinec D'Angelo, PhD
Organizational Affiliation
Ottawa Heart Institute Research Corporation
Official's Role
Study Chair
Facility Information:
Facility Name
University of Ottawa Heart Institute
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Y 4W7
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
24246588
Citation
Reid RD, McDonnell LA, Riley DL, Mark AE, Mosca L, Beaton L, Papadakis S, Blanchard CM, Mochari-Greenberger H, O'Farrell P, Wells GA, Slovinec D'Angelo ME, Pipe AL. Effect of an intervention to improve the cardiovascular health of family members of patients with coronary artery disease: a randomized trial. CMAJ. 2014 Jan 7;186(1):23-30. doi: 10.1503/cmaj.130550. Epub 2013 Nov 18.
Results Reference
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Family Heart Health Program: Randomized, Controlled Trial

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