Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12618001391268
Ethics application status
Approved
Date submitted
14/08/2018
Date registered
20/08/2018
Date last updated
23/04/2020
Date data sharing statement initially provided
23/04/2020
Type of registration
Prospectively registered

Titles & IDs
Public title
Specialised Fibre Supplement in Type 1 Diabetes
Scientific title
The safety, feasability and tolerability of a high amylose maize starch modified by acetylation and butyrylation in adults with type 1 diabetes.
Secondary ID [1] 295807 0
None
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Type 1 diabetes 309242 0
Condition category
Condition code
Metabolic and Endocrine 308118 308118 0 0
Diabetes

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
This trial is a single arm, safety, tolerability and feasibility trial of a fibre supplement in adults with type 1 diabetes. The supplement is a high-amylose maize starch modified by acetylation and butyrylation. The supplement will be administered to adult participants at a dose of 40g/day for 6 weeks. The dose will be divided in two daily 20g doses, taken at a similar time each day, and combined with warmed or cold food of their choice (e.g. sauces, soups, yoghurt).
To improve tolerability, participants will start at 25% of the total dose (i.e. 10g/day) and increase the dose in 10g increments every 2 days. If the increased dose is not tolerated, the participant will remain on the previous dose for an additional 2 days before attempting the increased dose again. If that dose is not tolerated after the third attempt, they will remain on the previous dose for the remainder of the intervention. Adherence to the intervention will be assessed through the supplement dose logbook and supplements returned in the following visit.
Intervention code [1] 312138 0
Treatment: Other
Comparator / control treatment
No control
Control group
Uncontrolled

Outcomes
Primary outcome [1] 307094 0
Feasibility of the study design. Feasibility will be assessed through recruitment and retention, compliance, withdrawal rate and data completion and accuracy. Recruitment and retention measures involve assessing the recruitment levels against target, withdrawal rates, timing and reasons as well as identifying barriers and opportunities in recruitment and retention. Compliance will be assessed through assessing unused supplement returned, proportion of doses recorded as consumed in the dose logbook and faecal short chain fatty acid measurements.
Timepoint [1] 307094 0
Recorded 3, 6, and 12 weeks after supplement administration
Primary outcome [2] 307108 0
Safety of the fibre supplement in the study population. Safety will be assessed through measuring toxicity, glycaemic control and incidence of adverse events. This will be measured through pathology of blood and urine, glycaemic control through the use of continuous glucose monitoring and side effects monitored through a validated 18 item, 5-point likert scale questionnaire to report any symptoms experienced since the previous visit with an additional 10 items included to capture diabetes-specific side effects. They will also be contacted by phone where notes and questionnaire responses will be recorded after 1 week of supplement administration.
For any serious adverse event or adverse reaction reported or detected will be reported immediately to the sponsor and the HREC which will be followed by a detailed written report and the participants may withdraw from the project at any time without affecting their relationship or usual clinical care.
Timepoint [2] 307108 0
Recorded at baseline before supplement administration and 1, 3 and 6 weeks after supplement administration.
Primary outcome [3] 307109 0
Tolerability of the supplement in the study population. This will be monitored through dose tolerability checked through gastrointestinal symptoms experienced (validated 18-item, 5-point likert scale questionnaire) and participant feedback (5-point likert scale questionnaire to record the acceptability and palatability of the supplement).
Timepoint [3] 307109 0
At baseline before supplement consumption and 3 and 6 weeks after supplement consumption commencement.
Secondary outcome [1] 350668 0
The effect of the specialised fibre supplement on plasma C-peptide, as an indicator of beta-cell function. It will be measured through a Mixed Meal Tolerance Test (MMTT). Plasma C-Peptide 2 hour area under the curve will be determined.
Timepoint [1] 350668 0
C-Peptide will be measured at baseline before supplement consumption and at 6 and 12 weeks post supplement consumption commencement.
Secondary outcome [2] 350718 0
The effect of the specialised fibre supplement on gut microbiome. Gut microbiome and proteome will be measured through stool samples which will be collected and analysed through DNA extraction for microbiome sequencing and faecal meta-proteomics, meta-genomic profiling to identify and quantify gut bacteria present and any shift in the community composition over time.
Timepoint [2] 350718 0
At baseline before supplement consumption and 6 and 12 weeks after supplement consumption commencement.
Secondary outcome [3] 350738 0
The effect of the specialised fibre supplement on changes in immune cell function. Immune cell phenotype will be measured through blood collection where mass flow cytometry analysis of immune cell phenotype will be performed to observe changes in ratio of regulatory to effector cell populations, antigen presenting cells etc.
Timepoint [3] 350738 0
At baseline before supplement consumption and 6 and 12 weeks after supplement consumption commencement.
Secondary outcome [4] 350762 0
The effect of the specialised fibre supplement on exogenous insulin requirements. Insulin will also be measured as the average total daily insulin dose with participant's usual record method (e.g. insulin pump downloads, smart blood glucose metres, smartphone application or paper-based logbooks).
Timepoint [4] 350762 0
Insulin records will be collected at baseline before supplement consumption and 3, 6 and 12 weeks post supplement consumption commencement.

Eligibility
Key inclusion criteria
• 18 to 45 years, males and females
• Clinical diagnosis of T1D for at least 6 months
• HbA1c less than or equal to 8.5%
• Willing and able to follow study protocol
• stable disease management
Minimum age
18 Years
Maximum age
45 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Current or planned pregnancy or lactation during the study
• Use of diabetes medications other than insulin that affect glucose homeostasis
• Hypoglycaemia unawareness
• Concomitant disease or treatment that may, in the judgment of the investigators, impact on glycaemic control, insulin requirements or other outcome measures
• History or symptoms of gastrointestinal disease or malabsorption, including coeliac disease
• Any known condition that could be associated with poor compliance (e.g. drug/alcohol abuse)
• Weight below 50kg and above 120kg (to ensure full dose between 0.33- 0.80g/kg/day)
• Known liver or renal disease
• Use of senor-augmented insulin therapy (i.e. Medtronic 640G pump with low glucose suspend)
• Unwillingness to maintain their normal stable diet during the study and/or following a restrictive diet that would impact their ability to take the supplement (e.g. intermittent fasting).
• Recent antibiotic usage (previous 6 weeks) or anticipated antibiotic usage during the study.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Safety
Statistical methods / analysis
This trial is a pilot study and therefore not designed to be sufficiently powered to assess changes in exploratory outcome measures.
We will use a Proof-of-Concept dual-criteria approach for assessing endpoints of feasibility and safety.
When reporting data, comparison will be made on an intention to treat (ITT) basis. Discrete variables will be summarized by frequencies and percentages. Continuous variables will be summarized by use of standard measures of central tendency and dispersion (mean and standard deviation and/or quantile points). Outcome variables will be summarized over time. Binary outcomes will be summarized by n and percentages with chisq tests performed if appropriate. Where necessary outcome variables with a skewed distribution will be log-transformed to achieve normality and relative change (%) used to express change from baseline. A 5% significance level will be used (unadjusted for multiple comparisons). All comparisons will be two sided.
For multi-omic datasets, univariate and supervised and unsupervised multivariate analyses will be performed to identify proteins, genes and taxa with the most predictive power to discriminate any effects of the supplement. Data visualization, cross-validation, permutation tests, and correlation analysis will be performed to further assess the significance and relationship between the proteins, genes and taxa identified. Pathway and network analyses will seek to identify metabolic pathways that may be altered in the dataset using gene enrichment analysis, KEGG orthologues, and assigning bacterial modules and hierarchies using the bioinformatics tools GOmixer and MetaCyc. Using integrative multivariate approaches, we will identify combinations of biological features which are associated with phenotype using the statistical mixOmics package in ‘R’. Potential confounders including BMI, age and sex will also be examined.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
4/09/2018
Actual
25/09/2018
Date of last participant enrolment
Anticipated
1/02/2019
Actual
21/02/2019
Date of last data collection
Anticipated
29/04/2019
Actual
31/05/2019
Sample size
Target
25
Accrual to date
Final
21
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 11665 0
Royal Prince Alfred Hospital - Camperdown
Recruitment postcode(s) [1] 23711 0
2050 - Camperdown

Funding & Sponsors
Funding source category [1] 300402 0
Charities/Societies/Foundations
Name [1] 300402 0
Juvenile Diabetes Research Foundation (JDRF) Australia
Country [1] 300402 0
Australia
Primary sponsor type
University
Name
Monash University
Address
Scenic Blvd & Wellington Road
Clayton VIC 3800
Country
Australia
Secondary sponsor category [1] 299858 0
None
Name [1] 299858 0
Address [1] 299858 0
Country [1] 299858 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 301208 0
Sydney Local Health District Ethics Review Committee (RPAH Zone) [EC00113]
Ethics committee address [1] 301208 0
Ethics committee country [1] 301208 0
Australia
Date submitted for ethics approval [1] 301208 0
11/06/2018
Approval date [1] 301208 0
02/07/2018
Ethics approval number [1] 301208 0
Protocol No. X18-0166

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

Contacts
Principal investigator
Name 86226 0
Dr Eliana Marino Moreno
Address 86226 0
Monash University
15 Innovation Walk, 75
Melbourne VIC, 3168
Country 86226 0
Australia
Phone 86226 0
+61 3 9902 4946
Fax 86226 0
Email 86226 0
[email protected]
Contact person for public queries
Name 86227 0
Kirstine Bell
Address 86227 0
Charles Perkins Centre (D17)
John Hopkins Dr
University of Sydney NSW 2006
Country 86227 0
Australia
Phone 86227 0
+61 2 8627 4250
Fax 86227 0
Email 86227 0
[email protected]
Contact person for scientific queries
Name 86228 0
Eliana Marino Moreno
Address 86228 0
Monash University
15 Innovation Walk, 75
Melbourne VIC, 3168
Country 86228 0
Australia
Phone 86228 0
+61 3 9902 4946
Fax 86228 0
Email 86228 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
What data in particular will be shared?
Deidentified participant data underlying published results
When will data be available (start and end dates)?
Following peer-reviewed publication (Start date to be determined). No end date determined.
Available to whom?
Case-by-case basis at the discretion of the Chief Investigators
Available for what types of analyses?
Analyses decided on a case-by-case basis at the discretion of the Chief Investigators
How or where can data be obtained?
Access subject to approvals by Chief Investigators (Contact Person: [email protected])


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
7742Study protocol  [email protected]
7743Informed consent form  [email protected]
7744Ethical approval  [email protected]



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 AINovel Strategies to Protect and Visualize Pancreatic ß Cells in Diabetes2020https://doi.org/10.1016/j.tem.2020.10.002
EmbaseDietary SCFAs Immunotherapy: Reshaping the Gut Microbiota in Diabetes.2021https://dx.doi.org/10.1007/5584_2020_515
EmbaseSCFAs in T1D: A microbiota-targeted approach for immune tolerance.2022https://dx.doi.org/10.1016/j.coemr.2022.100355
N.B. These documents automatically identified may not have been verified by the study sponsor.