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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02903615
Registration number
NCT02903615
Ethics application status
Date submitted
5/06/2016
Date registered
16/09/2016
Titles & IDs
Public title
Optimising Health in Type 1 Diabetes
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Scientific title
The Optimal Diet for Optimising Health in Type 1 Diabetes
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Secondary ID [1]
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16/053
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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:
Diabetes Mellitus
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Condition category
Condition code
Metabolic and Endocrine
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Other interventions - Novel diet
Other interventions - Standard diet
Experimental: Novel type 1 diet - Experimental diet to be examined: altered macronutrient composition: lower carbohydrate, Mediterranean-style, prebiotic fibre focus.
Placebo comparator: Standard therapy - Standard dietary therapy, as promulgated by Australian standards
Other interventions: Novel diet
Novel diet to optimise glucose levels and minimise systemic inflammation: altered macronutrient composition: lower carbohydrate, Mediterranean-style, prebiotic fibre focus.
Other interventions: Standard diet
Standard diabetes diet recommendations
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Intervention code [1]
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Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Glucose control
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Assessment method [1]
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HbA1c
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Timepoint [1]
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3 months
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Secondary outcome [1]
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Inflammation
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Assessment method [1]
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Circulating immune cells numbers
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Timepoint [1]
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3 months
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Secondary outcome [2]
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Gut microbiome
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Assessment method [2]
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Gut flora subtypes
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Timepoint [2]
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3 months
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Secondary outcome [3]
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C-peptide
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Assessment method [3]
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Urinary excretion
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Timepoint [3]
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3 months
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Secondary outcome [4]
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postprandial glucose excursion
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Assessment method [4]
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postprandial glucose excursion
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Timepoint [4]
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3 months
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Secondary outcome [5]
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Follow-up of glycemic control and insulin secretion
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Assessment method [5]
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HbA1c, urinary C-peptide
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Timepoint [5]
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12 and 24 months
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Eligibility
Key inclusion criteria
* type 1 diabetes
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Minimum age
18
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?
Yes
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Key exclusion criteria
* Women lactating, pregnant or of childbearing potential who are not willing to avoid becoming pregnant during the study.
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/09/2016
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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
30/06/2020
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Sample size
Target
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Accrual to date
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Final
13
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Recruitment in Australia
Recruitment state(s)
NSW
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Recruitment hospital [1]
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professor Katherine Samaras - Sydney
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Recruitment hospital [2]
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Garvan Institute to Medical Research - Sydney
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Recruitment postcode(s) [1]
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2010 - Sydney
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Recruitment postcode(s) [2]
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- Sydney
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Funding & Sponsors
Primary sponsor type
Other
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Name
Garvan Institute of Medical Research
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Type 1 diabetes is an autoimmune condition where circulating immune cells destroy the beta-cells in the pancreas that make insulin, resulting in a degree of insulin deficiency, whereby blood glucose levels rise and diabetes develops. When there is severe insulin deficiency, life-threatening ketoacidosis can develop. Treatment is lifelong insulin replacement therapy; dietary intervention is a also cornerstone of glucose management. The Optimise Diet is a multi-pronged diet based on "best health" principles: to minimise blood glucose rises after eating, reduce the immune cells involved in destruction of the insulin-secreting beta-cells, and improve the gut microbiome and systemic inflammation. In this study, its effects will be compared to the Standard Diabetes Diet that is currently recommended in Australia and internationally.
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Trial website
https://clinicaltrials.gov/study/NCT02903615
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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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Katherine Samaras, MD PhD FRACP
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Address
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Garvan Institute of Medical Research
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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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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 scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Undecided
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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
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02903615