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Trial registered on ANZCTR
Registration number
ACTRN12612000687897
Ethics application status
Approved
Date submitted
5/06/2012
Date registered
26/06/2012
Date last updated
27/06/2012
Type of registration
Prospectively registered
Titles & IDs
Public title
The effect of consuming a meal consisting of potato or sweetpotato on the feelings of hunger/ fullness and health related blood measurements
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Scientific title
The effect of consuming potato and sweetpotato by healthy adults on post-prandial satiety, glycaemia and oxidative stress biomarkers related to chronic disease prevention.
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Secondary ID [1]
280382
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Nil
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Universal Trial Number (UTN)
U1111- 1130- 0473
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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:
Obesity
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Diabetes
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Condition category
Condition code
Diet and Nutrition
286668
286668
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0
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Obesity
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Metabolic and Endocrine
286669
286669
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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
Prevention
Description of Test meal:
The meal consists of 400g of potato/ sweetpotato, 30g of low fat salad dressing, 5g of spring onion as garnish and 0.5 g of salt
Duration of administration: Participants will fast overnight only consuming water (after consuming a standard dinner provided to them the night before the test day). The entire meal will be consumed within 10 minutes.
Time of administration: In the morning for breakfast (8 am - 12 pm)
Frequency of administration: Once every alternate week for 10 weeks
Number of interventions: 5
Intervention 1: Cooked sweetpotato (hot)
Intervention 2: Cooked sweetpotato (cooled for 24 hours at 4 degrees; served cold)
Intervention 3: Cooked potato (hot)
Intervention 4: Cooked potato (cooled for 24 hours at 4 degrees celcius )
Intervention 5: White bread as control
Duration of intervention and wash out period between intervention: Each participant will visit 5 times (once every alternate week for a duration of 10 weeks with a wash out period of 2 weeks between interventions
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Intervention code [1]
284745
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Prevention
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Comparator / control treatment
Active control (Conventional study)
Control: White bread
Quantity administered: 50g available carbohydrate portion
Frequency of administration: Once as part of the 5 arm within participant post-prandial study
Duration of control intervention: one breakfast meal (Conventional study)
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Control group
Active
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Outcomes
Primary outcome [1]
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Post-prandial satiety response by Labelled Magnitude Satiety line scale
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Assessment method [1]
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Timepoint [1]
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Fasting then immediately,10, 25, 40, 55, 85, 115, 175 minutes after the start of the meal
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Primary outcome [2]
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Post-prandial blood glucose response of finger prick blood samples using a glucometer
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Assessment method [2]
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Timepoint [2]
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Fasting then 15, 30, 45, 60, 90 and 120 minutes after the start of the test meal
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Primary outcome [3]
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Post-prandial insulin by ELISA assay of venous blood serum
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Assessment method [3]
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Timepoint [3]
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Fasting then 30, 60, 120 and 180 minutes after the start of the test meal.
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Secondary outcome [1]
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Ghrelin by ELISA assay on venous blood plasma
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Assessment method [1]
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Timepoint [1]
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Fasting then 30, 60, 120 and 180 minutes after the start of the test meal
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Secondary outcome [2]
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Isoprostane by High Performance Liquid Chromatography on venous blood plasma
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Assessment method [2]
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Timepoint [2]
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Fasting then 30, 60, 120 and 180 minutes after the start of the test meal
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Secondary outcome [3]
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Interleukin- 6 by ELISA Interleukin kit on venous blood plasma
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Assessment method [3]
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Timepoint [3]
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Fasting then 30, 60, 120 and 180 minutes after the start of the test meal
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Secondary outcome [4]
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Antioxidant capacity by Im An ox Kit on venous serum blood plasma
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Assessment method [4]
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Timepoint [4]
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Fasting then 30, 60, 120 and 180 minutes after the start of the test meal
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Secondary outcome [5]
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Nitric oxide by Micro ion selective method on venous blood plasma
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Assessment method [5]
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Timepoint [5]
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Fasting then 30, 60, 120 and 180 minutes after the start of the meal
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Secondary outcome [6]
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Chlorogenic acid by High Performance Liquid Chromatography on venous blood plasma
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Assessment method [6]
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Timepoint [6]
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Fasting then 30, 60, 120 and 180 minutes after the start of the meal
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Eligibility
Key inclusion criteria
30 healthy adults (from the general population)
Age range: 18 to 65 Years
BMI: 18.5- 29.5 Kg/m^2
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
(1) Smokers
(2) Pregnant women
(3) Individuals consuming more than 3 alcoholic drinks per day (1 standard alcoholic drinks per day contains 10 g of pure alcohol)
(4) Individuals with food allergies
(5) People taking medication known to affect study parameters
(6) Individuals with eating disorders (Eating disorders will be determined by the 3 factor eating questionniare
(7) Individuals with history of the following conditons:
(a) Diabetes
(b) Cardiovascular diseases
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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)
Allocation is not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation will be done using a randomised table created by a computer software (computerised sequence generation).
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Crossover
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
16/07/2012
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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
25
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Curtin University
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Address [1]
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Kent street
Bentley
WA 6102
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Country [1]
285166
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Australia
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Funding source category [2]
285167
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Commercial sector/Industry
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Name [2]
285167
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Horticulture Australia Limited ( HAL)
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Address [2]
285167
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Level 7
179, Elizabeth Street
Sydney
NSW 2000
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Country [2]
285167
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Australia
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Primary sponsor type
Individual
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Name
Dr Stuart K Johnson (Principle Investigator)
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Address
Room 361, Level 3
School of Public Health (Buliding 400)
Curtin University
Kent street
Bentley Campus
WA 6102
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Associate Professor Vicky Solah
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Address [1]
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Room 353, Level 3
School of Public Health (Buliding 400)
Curtin University
Kent street
Bentley Campus
WA 6102
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Country [1]
284033
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Australia
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Secondary sponsor category [2]
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Individual
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Name [2]
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Dr Tony James
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Address [2]
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Room 358, Level 3
School of Public Health
Curtin University
Kent street
Bentley Campus
WA 6102
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Country [2]
284034
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Ms Janine Wright
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Address [1]
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Room 354, Level 3
School of Public Health
Curtin University
Kent street
Bentley Campus
WA 6102
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Country [1]
260789
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Australia
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Other collaborator category [2]
260790
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Individual
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Name [2]
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Dr Cyril Mamotte
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Address [2]
260790
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Room 207, Level 2
School of Biomedical Sciences
Hayman road
Curtin University
Bentley Campus
WA 6102
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Country [2]
260790
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Australia
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Other collaborator category [3]
260791
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Individual
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Name [3]
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Dr Le Jian
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Address [3]
260791
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Room 359, Level 3
School of Public Health
Kent Street
Curtin University
Bentley Campus
WA 6102
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Country [3]
260791
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Australia
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Other collaborator category [4]
260792
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Individual
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Name [4]
260792
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Dr Ya Ping Lee
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Address [4]
260792
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Room 207, Level 2
School of Pharmacy
Hayman road
Curtin University
Bentley Campus
WA 6102
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Country [4]
260792
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
287177
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Curtin University Human Research Ethics Committee
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Ethics committee address [1]
287177
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Office of Research and Development PO Box U1987 Bentley Campus Perth WA 6845
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Ethics committee country [1]
287177
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Australia
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Date submitted for ethics approval [1]
287177
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04/04/2012
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Approval date [1]
287177
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31/05/2012
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Ethics approval number [1]
287177
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HR 47/2012
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Summary
Brief summary
This study will investigate the effect of different varieties of sweetpotatoes and potatoes prepared by different methods on feeling of hunger/ fullness and other blood measurements related to health after consumption of a test meal. The significance of this study is to identify which types of potatoes and sweetpotatoes reduce hunger the most and lower blood glucose, insulin, ghrelin and oxidative stress biomarkers and thus may be recommended as part of a healthy diet in order to reduce the risk of obesity, diabetes and heart disease.
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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
34103
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Country
34103
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Phone
34103
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Fax
34103
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Email
34103
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Contact person for public queries
Name
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Komal Tulsidas
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Address
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School of Public Health
Curtin University
Kent street
Bentley
WA 6012
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Country
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Australia
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Phone
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+61 8 9266 4465
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Fax
17350
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+61 8 9266 2958
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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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Dr Stuart K Johnson
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Address
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School of Public Health
Curtin University
Kent street
Bentley
WA 6102
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Country
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Australia
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Phone
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+61 8 9266 9486
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Fax
8278
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+61 8 9266 2958
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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.
Download to PDF