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The effects of acute and long-term apple consumption on risk factors for cardiovascular disease

Not Applicable
Completed
Conditions
Cardiovascular Disease
Gut Microbiome
Cardiovascular - Diseases of the vasculature and circulation including the lymphatic system
Cardiovascular - Hypertension
Oral and Gastrointestinal - Normal oral and gastrointestinal development and function
Registration Number
ACTRN12615000361505
Lead Sponsor
The University of Western Australia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
30
Inclusion Criteria

We are looking for volunteers with one or more of the following:
-Slightly elevated blood pressure (120 < systolic BP < 160)
-High blood sugar (5.6 < glucose < 6.5)
-High cholesterol (5 < total cholesterol < 8)
-Central obesity (men > 94cm; women > 80cm)
It is critical to the study that participants are not currently taking any blood pressure or cholesterol lowering medication.

Exclusion Criteria

- Current or recent (12 months) smoking
- Body mass index less than 18 or greater than 40 kg/m2
- History of cardiovascular or peripheral vascular disease
- A systolic blood pressure less than 100 or greater than 160 mmHg.
- A diastolic blood pressure less than 50 or greater than 100 mmHg
- Diagnosed diabetes, and non-diabetic individuals with fasting plasma glucose concentrations greater than 6.5 mmol/L
- A psychiatric illness
- Other major illnesses such as cancer
- Current or recent (within previous 6 months) significant weight loss or gain ( greater than 6% of body weight) or actively trying to lose weight
- Alcohol intake greater than 210g per week for women and greater than 280 g per week for men
- Women who are lactating, pregnant or wishing to become pregnant during the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Primary outcome: % Flow-mediated dilatation of the brachial artery assesed by ultrasonogaphy. [Timepoint for chronic intervention: Baseline and 4 weeks after intervention commencement <br>Timepoint for acute intervention: Baseline and 2 hours after intervention]
Secondary Outcome Measures
NameTimeMethod
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