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Trial registered on ANZCTR


Registration number
ACTRN12609000175279
Ethics application status
Approved
Date submitted
4/03/2009
Date registered
16/04/2009
Date last updated
16/04/2009
Type of registration
Retrospectively registered

Titles & IDs
Public title
The chronic effects of whey protein isolate on metabolic syndrome risk factors in overweight and obese individuals
Scientific title
The chronic effects of whey protein isolate on metabolic syndrome risk factors in overweight and obese individuals
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Metabolic risk factors in overweight and obese individuals 4418 0
Condition category
Condition code
Diet and Nutrition 4682 4682 0 0
Obesity

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Chronic, randomized, parallel design study with 3 intervention groups where subjects consume 30g of either whey protein isolate, casein protein or glucose (control) in powder form mixed with 250ml water twice a day over a 12 week period while maintaining their usual diet and exercise regime
Intervention code [1] 4160 0
Other interventions
Comparator / control treatment
Placebo is 30g glucose (same dose as whey & casein) in powder form mixed with 250ml water for the control group twice a day
Control group
Placebo

Outcomes
Primary outcome [1] 5545 0
Improved blood lipid, lipoprotein profile, glucose tolerance and insulin response
Timepoint [1] 5545 0
Blood samples taken a 0, 6 and 12 weeks
Primary outcome [2] 5546 0
Improved blood pressure after 12 weeks. Blood pressure will be measured by research assistant using a Systolic blood pressure (SBP), diastolic blood pressure (DBP) measured on the left arm of participants with an automated sphygmomanometer (Dinamap ProCare). Subjects rested in a supine position before and during measurements.
Timepoint [2] 5546 0
Measured at 0, 6 and 12 weeks
Primary outcome [3] 5547 0
Reduced body fat mass & preserved or increased muscle mass
Timepoint [3] 5547 0
Measured by Dual-energy X-ray Absorptiometry (DEXA) at 0 and 12 weeks plus
Weight and anthropometric measures taken at 0, 6 and 12 weeks
Secondary outcome [1] 9342 0
Improved vascular endothelium function via Sphygmocor pulse wave analysis (PWA)
Timepoint [1] 9342 0
PWA readings at 0, 6 and 12 weeks

Eligibility
Key inclusion criteria
Body Mass Index (BMI) between 25-35kg/m2
Not on regular medications
Non-smoker
Have low dairy intake (<1-2 serves/day)
Less than 1 alcoholic drink/day for women, 2 for men
Weight stable
No major diseases or disorders
Minimum age
18 Years
Maximum age
65 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Smokers
On regular medications, especially those affecting blood pressure, thryoid, blood lipids
High consumption of dairy or alcohol
Taking regular supplements, vitamins, herbal remedies
On a weight loss regime

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
numbered containers
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation by using a randomisation table from a statistic book
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
18/04/2008
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
90
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 4612 0
Commercial sector/Industry
Name [1] 4612 0
Dairy Australia
Country [1] 4612 0
Australia
Primary sponsor type
Commercial sector/Industry
Name
Dairy Australia
Address
Locked Bag 104 Flinders Lane
Victoria 8009
Country
Australia
Secondary sponsor category [1] 4330 0
Commercial sector/Industry
Name [1] 4330 0
Dairy Australia
Address [1] 4330 0
Locked Bag 104 Flinders Lane
Victoria 8009
Country [1] 4330 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 6656 0
Curtin University Human Ethics Committee
Ethics committee address [1] 6656 0
Ethics committee country [1] 6656 0
Australia
Date submitted for ethics approval [1] 6656 0
Approval date [1] 6656 0
12/11/2007
Ethics approval number [1] 6656 0
HR 149/2007

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 29350 0
Address 29350 0
Country 29350 0
Phone 29350 0
Fax 29350 0
Email 29350 0
Contact person for public queries
Name 12597 0
Assoc Prof Sebely Pal
Address 12597 0
School of Public Health
Curtin University
GPO Box U1987
Perth WA 6845
Country 12597 0
Australia
Phone 12597 0
+61 8 9266 4755
Fax 12597 0
+61 8 9266 2958
Email 12597 0
[email protected]
Contact person for scientific queries
Name 3525 0
Assoc Prof Sebely Pal
Address 3525 0
School of Public Health
Curtin University
GPO Box U1987
Perth WA 6845
Country 3525 0
Australia
Phone 3525 0
+61 8 9266 4755
Fax 3525 0
+61 8 9266 2958
Email 3525 0
[email protected]

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
SourceTitleYear of PublicationDOI
Dimensions AIEffects of whey protein isolate on body composition, lipids, insulin and glucose in overweight and obese individuals2010https://doi.org/10.1017/s0007114510000991
Dimensions AIComparative effects of whey and casein proteins on satiety in overweight and obese individuals: a randomized controlled trial2014https://doi.org/10.1038/ejcn.2014.84
N.B. These documents automatically identified may not have been verified by the study sponsor.