Cardiovascular Disease Clinical Trial
Official title:
The Impact of Portion Plates for Weight Loss on Cardiac Rehabilitation Patients
The study will involve cardiac rehabilitation clients and will measure their weight, height,
waist circumference and blood pressure comparisons between first and final visit (after 8
weeks). A control group will receive usual care and an experimental group will receive usual
care plus a portion control plate for their meals. Patients currently have their waist
circumference, weight, height and blood pressure measured at their first visit (week 0) and
at their final visit (week 8). This study would compare these three parameters at these same
times (week 0 and week 8) between the control and experimental groups. The control group
would receive the usual care while the experimental group would receive usual care plus be
given a portion control plate at week 0.
The hypothesis of this study is that subjects from the experimental group will have an
average reduction in: (a) waist circumference by > 5%, (b) weight or BMI by > 5%, and (c)
systolic and diastolic blood pressure by >10%. The subjects in the control group are
hypothesized to show an average less than these targets for the experimental group.
Status | Not yet recruiting |
Enrollment | 90 |
Est. completion date | February 2011 |
Est. primary completion date | February 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: - patients attending the cardiac rehab program who have a waist circumference of more than 102 cm (males) and 89 cm (females) Exclusion Criteria: - any patients with a waist circumference below the above levels |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
Canada | Richmond Health Services, Cardiac Rehabilitation | Richmond | British Columbia |
Lead Sponsor | Collaborator |
---|---|
Richmond Health Services |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Reduce waist circumference by 5% or more in intervention group | 8 weeks | No | |
Secondary | Reduce weight or BMI by 5% or more in intervention group | 8 weeks | No | |
Secondary | Reduce diastolic and systolic blood pressure by 10% or more in intervention group | 8 weeks | No |
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