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Trial registered on ANZCTR
Registration number
ACTRN12605000248662
Ethics application status
Approved
Date submitted
29/08/2005
Date registered
31/08/2005
Date last updated
8/06/2021
Date data sharing statement initially provided
8/06/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
Meal Replacement Study
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Scientific title
Study of Meal Replacement with Formula Diet in achieving weight loss and improved metabolic control in people with type 2 diabetes
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Secondary ID [1]
304434
0
Nil known
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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:
Type 2 diabetes
335
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Condition category
Condition code
Metabolic and Endocrine
387
387
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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 will be randomised to either group A (diet) or B (meal replacement) for a period of six months. Group A will receive conventional low calorie diet and physical activity guidance once per month during the six months and Group B will receive the same advice and in addition replace one meal each day with a meal replacement, Microdiet (MD).
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Intervention code [1]
292
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Lifestyle
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Comparator / control treatment
Conventional low calorie diet and physical activity guidance once per month
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Control group
Active
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Outcomes
Primary outcome [1]
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Change in body weight between baseline and 6 months.
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Assessment method [1]
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Timepoint [1]
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Change in body weight between baseline and 6 months
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Secondary outcome [1]
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Change in metabolic control of diabetes
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Assessment method [1]
975
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Timepoint [1]
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At three and six months as measured by HbA1C%, blood pressure and lipids (TG, TC, HDL-C & LDL-C).
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Eligibility
Key inclusion criteria
Type 2 diabetes. Body mass index > 29kg/m2.
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Minimum age
30
Years
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Maximum age
70
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Severe underlying disease prohibiting low calorie diet therapyAllergy to MDPregnant or breastfeedingNeed for protein restrictionGP considers the participant inappropriate.
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Study design
Purpose of the study
Treatment
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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 envelopes are held by an independent person, and opened by the independent person to assign the intervention group
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer-generated random numbers (using Microsoft Excel), in blocks of 2-8 are used. These are stratified by diabetes treatment modality into 2 strata - insulin or non-insulin controlled.
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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
Phase 3
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Type of endpoint/s
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
3/06/2005
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Actual
21/06/2005
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Date of last participant enrolment
Anticipated
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Actual
1/08/2005
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Date of last data collection
Anticipated
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Actual
1/03/2006
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Sample size
Target
40
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Accrual to date
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Final
41
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
439
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Commercial sector/Industry
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Name [1]
439
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Sunny Health Co.
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Address [1]
439
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Yaesu Center Bldg, 5F, 1-6-6 Yaesu
Chuo-ku, Tokyo, Japan 103-0028
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Country [1]
439
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Japan
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Primary sponsor type
Commercial sector/Industry
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Name
Sunny Health Co., Japan
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Address
Yaesu Center Bldg, 5F, 1-6-6 Yaesu
Chuo-ku, Tokyo, Japan 103-0028
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Country
Japan
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Secondary sponsor category [1]
357
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None
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Name [1]
357
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None
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Address [1]
357
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Country [1]
357
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1412
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International Diabetes Institute
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Ethics committee address [1]
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
1412
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Approval date [1]
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21/03/2005
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Ethics approval number [1]
1412
0
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Summary
Brief summary
Mean (± SEM) weight loss adjusted for baseline values was significantly greater in the meal replacement group (n=20) than the control group (n=21) at three months (4.7± 0.8 vs 1.3 ± 0.8 kg, P=0.007) and at six months (5.0± 5.2 vs 1.5± 5.2 kg, P=0.04) (Figure 1). The reduction in waist circumference was 1.4 cm greater in the meal replacement group than the control group at six months, but this difference was not significant. BMI reduced by 1.8kg/m2 in the meal replacement group and by 0.6kg/m2 in the control group (P=0.05).
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Trial website
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Trial related presentations / publications
No publication.
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Jonathan Shaw
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Address
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Baker IDI Heart and Diabetes Institute
99 Commercial Road
Melbourne 3004
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Country
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Australia
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Phone
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+61 3 8532 1821
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Miss Cathie Adams
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Address
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International Diabetes Institute
250 Kooyong Road
Caulfield VIC 3162
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Country
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Australia
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Phone
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+61 3 92585000
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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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Associate Professor Jonathan Shaw
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Address
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Baker IDI Heart and Diabetes Institute
99 Commercial Road
Melbourne 3004
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Country
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Australia
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Phone
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+61 3 8532 1821
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Fax
409
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Email
409
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
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No/undecided IPD sharing reason/comment
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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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