Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12611000257965
Ethics application status
Approved
Date submitted
28/02/2011
Date registered
9/03/2011
Date last updated
31/05/2011
Type of registration
Retrospectively registered

Titles & IDs
Public title
Assessing the impact of a sweetened beverage tax in Australia
Scientific title
Assessing the impact of a 10%, 20% and 30% increase in the price of sweetened drinks, versus no increase, on the purchase intentions of beverages for household consumption.
Secondary ID [1] 259687 0
Nil
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Obesity 261256 0
diet 261257 0
Nutrition 261258 0
Condition category
Condition code
Public Health 259412 259412 0 0
Other public health

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Participants allocated to the one of three beverage tax conditions.

During a telephone survey, participants will be read a list of beverages typically available from an Australian supermarket. The survey will be conducted once only.

For each beverage product type, participants will be provided with information about the price and container sizes (up to three) which the product can be purchased (for example, a 2 litre bottle, a 1.5 litre bottle and a 600ml bottle) based on data regarding the most frequently purchased container size for that beverage product.

For each beverage type, participants will be asked to report the number of products (in each container size), they would intend to purchase for the consumption of their household during a typical grocery shop.

The price of beverages containing caloric sweetener will be experimentally manipulated.

For group 1: the price of such products will be increased by 10%

For group 2: the price of such products will be increased by 20%

For group 3: the price of such products will be increased by 30%
Intervention code [1] 258115 0
Lifestyle
Intervention code [2] 264185 0
Prevention
Comparator / control treatment
The comparison group (group 4) procedure will be identical to those in the intervention conditions, however the price of beverages read to control group participants will not be inflated, and will be at current market price
Control group
Active

Outcomes
Primary outcome [1] 262216 0
Mean Kilojoules per household of beverages intended to be purchased for household consumption (by group)
Timepoint [1] 262216 0
This is a cross sectional survey so there is only one time point. Data will be assessed once all the survey results have been collected
Secondary outcome [1] 273346 0
Nil
Timepoint [1] 273346 0
Nil

Eligibility
Key inclusion criteria
Participants will be sampled from a cohort of adults previously recruited into a random household general health telephone survey and who agreed to be approach for future opportunities for research participation. Additionally, to be eligible, participants must be 16 years or older be able to converse in English and have some current responsibility for household grocery shopping.
Minimum age
16 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
nil

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Participants will be telephoned and approached to participate in the study. Participants will be randomly allocated into 4 groups in a ratio of 1:1:1:1
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
the randomisation procedure will be generated using computer software built into the the computerised telephone survey system
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
3/03/2011
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
800
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 258572 0
University
Name [1] 258572 0
University of Newcastle
Country [1] 258572 0
Australia
Primary sponsor type
Individual
Name
Luke Wolfenden
Address
The University of Newcastle
School of Medicine and Public Health
University Dr, Callaghan, NSW, 2308
Australia
Country
Australia
Secondary sponsor category [1] 257712 0
None
Name [1] 257712 0
Address [1] 257712 0
Country [1] 257712 0
Other collaborator category [1] 251834 0
Government body
Name [1] 251834 0
Hunter New England Population Health
Address [1] 251834 0
Hunter New England Population Health
Longworth Ave, Wallsend, NSW, 2287
Australia
Country [1] 251834 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 260556 0
Hunter New England Human Research Ethics Committee
Ethics committee address [1] 260556 0
Ethics committee country [1] 260556 0
Australia
Date submitted for ethics approval [1] 260556 0
Approval date [1] 260556 0
04/09/2009
Ethics approval number [1] 260556 0
09/06/17/4.03

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

Contacts
Principal investigator
Name 32276 0
Address 32276 0
Country 32276 0
Phone 32276 0
Fax 32276 0
Email 32276 0
Contact person for public queries
Name 15523 0
luke wolfenden
Address 15523 0
C/O Hunter New England Population Health, Locked Bag 10, Wallsend, NSW, 2287
Country 15523 0
Australia
Phone 15523 0
+61249246247
Fax 15523 0
Email 15523 0
[email protected]
Contact person for scientific queries
Name 6451 0
luke wolfenden
Address 6451 0
C/O Hunter New England Population Health, Locked Bag 10, Wallsend, NSW, 2287
Country 6451 0
Australia
Phone 6451 0
+61249246247
Fax 6451 0
Email 6451 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
No additional documents have been identified.