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Trial registered on ANZCTR
Registration number
ACTRN12610000852055
Ethics application status
Approved
Date submitted
13/10/2010
Date registered
13/10/2010
Date last updated
9/02/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
Dietary approaches for treatment of the metabolic syndrome in overweight and obese women.
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Scientific title
A randomised, controlled dietary intervention to evaluate the effect of a high protein diet compared with a high carbohydrate, high fibre diet on individual components of the metabolic syndrome and markers of cardiovascular disease risk in overweight and obese women.
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Secondary ID [1]
252855
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Metabolic syndrome in overweight and obese women
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Diabetes prevention in overweight and obese women
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Insulin resistance in overweight and obese women
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Condition category
Condition code
Diet and Nutrition
258549
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0
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Obesity
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Metabolic and Endocrine
258550
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0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants were randomised to one of two diets for eight weeks:
1. A hypocaloric (approximately 5500kJ/day) high protein diet (30% protein, 30% fat, 40% carbohydrate, ~25g total dietary fibre per day).
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Intervention code [1]
257373
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Lifestyle
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Intervention code [2]
257384
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Prevention
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Intervention code [3]
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Treatment: Other
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Comparator / control treatment
2. A hypocaloric (approximate 5500kJ/day) high carbohydrate, high fibre diet (20% protein, 30% fat, 50% carbohydrate, >35g total dietary fibre per day).
All participants were required to lose 5-10% of their initial bodyweight over the eight weeks by eating a diet specified in the guidelines prvided to them, and met with a study researcher on a fortnightly basis for a 30 minute nutritional counselling session and to be weighed.
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Control group
Active
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Outcomes
Primary outcome [1]
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Body weight (determined using electronic calibrated scales) and waist circumference (determined using a tape measure at the midpoint between the anterior superior iliac spine of the hip and bottom of the ribcage).
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Assessment method [1]
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Timepoint [1]
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Baseline and week 8
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Primary outcome [2]
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Total body fat, total lean mass and trunkal fat mass (measured by Dual Energy X-ray Anthropometry).
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Assessment method [2]
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Timepoint [2]
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Baseline and week 8.
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Primary outcome [3]
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Blood lipids, blood glucose, blood pressure and insulin sensitivity as measured by the Homeostasis Model Assessment for Insulin Resistance and by the McAuley Index.
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Assessment method [3]
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Timepoint [3]
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Baseline and week 8.
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Secondary outcome [1]
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Fasting plasma insulin, C-reactive protein, adiponectin, tumor necrosis factor alpha (TNF-alpha), plasminogen activator inhibitor -1 (PAI-1), interleukins 6, 8 and 18, grehlin, magnesium and serum uric acid.
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Assessment method [1]
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Timepoint [1]
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Baseline and week 8.
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Eligibility
Key inclusion criteria
Overweight (body mass index (BMI)> 27kg/m^2). Weight stable over last 3 months. Prepared to undergo dietary intervention and eat substantial amounts of dietary fibre including wholegrains, legumes and pulses.
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
No diabetes, psychiatric illness, drug or alcohol dependence that would affect ability to adhere to the dietary guidelines. No history of an eating disorder or renal or hepatic failure. Not on lipid lowering medications or medications known to affect metabolism. Not pregnant, lactating or planning to become pregnant in the next 8 weeks.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelopes containing treatment assignation was prepared by a research assistant who was not involved in the study in any other way, and allocation to participants was in sequential order.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Individuals were randomised to treatment groups stratified by age and body mass index. Strata were randomised in random sized blocks using the randomisation commands in Microsoft Excel.
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
26/05/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
80
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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New Zealand
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State/province [1]
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Funding & Sponsors
Funding source category [1]
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Other Collaborative groups
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Name [1]
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Riddet Institute
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Address [1]
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Private Bag 11222
Palmerston North 4442
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Country [1]
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New Zealand
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Primary sponsor type
Individual
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Name
Professor Jim Mann
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Address
Department of Human Nutrition
University of Otago
PO Box 56
Dunedin 9054
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Country
New Zealand
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Secondary sponsor category [1]
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Individual
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Name [1]
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Lisa Te Morenga
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Address [1]
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Department of Human Nutrition
University of Otago
PO Box 56
Dunedin 9054
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Country [1]
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New Zealand
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Otago Human Ethics Committee
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Ethics committee address [1]
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Ethics committee country [1]
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New Zealand
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Date submitted for ethics approval [1]
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Approval date [1]
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26/03/2008
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Ethics approval number [1]
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1/08/0028
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Summary
Brief summary
The metabolic syndrome is defined by a number of associated risk factors that cluster together in individuals increasing their risk of diabetes and heart disease. These factors include insulin resistance, abdominal obesity, high blood pressure, dyslipidaemia and raised blood sugar. The likelihood of dying of heart disease is increased three-fold in people with metabolic syndrome (diagnosed as having at least three risk factors). There is limited reporting on the prevalence of the metabolic syndrome in New Zealand, but reports suggest it could be more than 20% in adult New Zealanders with more than double the prevalence in adult Maori and Pacific Islanders. Correspondingly an estimated 7% of New Zealand adults have suffered a non-fatal heart disease event and the prevalence of diagnosed diabetes in New Zealand is estimated to be 4% in the general New Zealand population and as high as 12% in Maori and Pacific Islanders. These are likely to be underestimates and the prevalence is further increased when including estimates of undiagnosed cases. Clearly, determining effective strategies for managing metabolic syndrome risk factors is warranted. A number of lifestyle interventions indicate that clinically important improvements in insulin sensitivity, body weight, hypertension and blood fats are achievable. However we currently have little indication of which dietary modifications will achieve the greatest change. Both dietary fibre and dietary protein have shown promise in numerous studies but results have been inconsistent and many questions remain unanswered. This study attempts determine the ways and extent to which metabolic syndrome risk factors can be influenced by high fibre and high protein diets.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Lisa Te Morenga
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Address
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Department of Human Nutrition,
University of Otago,
PO Box 56,
Dunedin 9054
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Country
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New Zealand
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Phone
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+64 3 479 3978
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Lisa Te Morenga
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Address
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Department of Human Nutrition,
University of Otago,
PO Box 56,
Dunedin 9054
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Country
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New Zealand
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Phone
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+64 3 479 3978
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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