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The Breakfast Rise, Education and Knowledge Study (BREAK)

Primary Purpose

type1diabetes

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
High glycaemic load breakfast meal
High glycaemic load breakfast meal with additional 10g protein
Medium glycaemic load breakfast meal
Sponsored by
University of Stirling
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for type1diabetes

Eligibility Criteria

5 Years - 17 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Children and young people aged between 5-17 years Diagnosis of type 1 diabetes for a minimum of one year On multiple daily injections (MDI) together with carbohydrate counting or Continuous Subcutaneous Insulin Infusion (CSII) using either open or closed loop systems. Use Dexcom continuous glucose monitoring (CGM) on a regular basis Have a Dexcom Clarity account and use the Clarity App Regularly eats a breakfast meal before midday Access to internet and email Exclusion Criteria: Prescribed anti-hyperglycaemia agents i.e. Glucophage (Metformin) and or antidepressants. Any other medical conditions that may impact on the digestion and or absorption of nutrients, including coeliac disease and gastroparesis. Vegans Allergic or intolerant to the test meals Experiencing difficulties with food including diagnosed eating disorders Currently actively taking part in another research study

Sites / Locations

  • Faculty of Health Sciences and Sport

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

Test meal 1

Test meal 2

Test meal 3

Arm Description

High glycaemic load breakfast meal

High glycaemic lead with additional 10g protein breakfast meal

Medium glycaemic load breakfast meal

Outcomes

Primary Outcome Measures

Mean glucose (mmol/l)
mmol/l

Secondary Outcome Measures

Mean peak glucose
mmol/l
Mean time to peak
minutes
Mean time to recover
minutes
Area under the glucose curve
mmol/minute
Range times (Time in range, time above range, time below range)
Percentage

Full Information

First Posted
December 2, 2022
Last Updated
February 28, 2023
Sponsor
University of Stirling
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1. Study Identification

Unique Protocol Identification Number
NCT05698875
Brief Title
The Breakfast Rise, Education and Knowledge Study
Acronym
BREAK
Official Title
The Breakfast Rise, Education and Knowledge Study in Children and Young People Who Have Type 1 Diabetes (T1D): The BREAK Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
February 14, 2023 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Stirling

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The study proposes to recruit 90 children and young people who have type 1 diabetes (T1D) and who regularly use Dexcom continuous glucose monitoring (CGM). The participants will be recruited from National Health Service (NHS) sites in the United Kingdom (UK) via their managing dietitian. The dietitian will be asked to provide baseline information about the participants which will include demographic data and information on clinical data, treatment and anthropometrics. Participants will be asked to provide access to Dexcom CGM data throughout the period of recording. Participants will be asked to test three breakfast meals (high glycaemic load, high glycaemic with 10g added protein and medium glycaemic load) plus a control meal (usual breakfast), repeating each meal twice in a randomized order using a Latin square randomisation. The dietitian will be asked to optimise the participants insulin doses prior to commencing test meals. Participants will be asked to complete a questionnaire for each of the postprandial test and control meal periods. This will include questions about their diabetes management, food and fluid intake in addition to questions on activities all of which took place during the three-hour postprandial period. The glycaemic response to the test and control meals will be analysed using the CGM data and the results statistically described using univariate, bivariate and multivariate analysis.
Detailed Description
This is a quantitative study. Dexcom CGM data will be collected for the period of recording. Participants will be asked to test three breakfast meals on two occasions and submit a postprandial questionnaire after each test meal to confirm it has been tested. The postprandial period will be three hours following the end of the breakfast test meal. The test meal recipes will be provided by the chief investigator. The dietary composition of the meals has been analysed using the a dietary analysis programme. The glycaemic index and load of the meals is estimated from this programme which uses available date from the international tables of glycaemic index and glycaemic loads (Atkinson et al. 2008; 2021). Most foods were based on average composition across different brands. For the added fibre bread used in test meal 3, an average of three known brands was used calculated by the chief investigator. The meals will be taken in the home environment with the food provided by the families. The participants will be asked to take the test meal on a day when their CGM reading is between 4-10mmol/l and when there has been no nocturnal hypoglycaemia on the night before the planned test. The participants will act as their own control. They will be asked to complete a postprandial questionnaire for control meals as well. The control meals will be there usual breakfast of choice. The study duration, commencing with the recruitment of the first participant and ending when data has been fully described, is anticipated to be two years. Recruitment Paediatric diabetes dietitians, working across the UK, will be enrolled to help recruit participants and become principal investigators (PI) for their site. Sample size The sample size power calculation is 64. This is based on using ANOVA repeated measures, within factors with four groups and measurements (3 test meals and control) with small effect size (0.15), P value 0.05 and power 0.80 and correlation among repeated measure of 0.5. The drop rate of clinical trials is often over 40%. Therefore, the aim is to recruit 90 participants to allow for this dropout rate and meet the sample size of 64. It may be possible to recruit this number of participants. There are approximately 29,000 children and young people living in the UK with T1D (Juvenile Diabetes Research Federation (JDRF), 2018). In the first phase of this study, 12 NHS sites were enrolled, and 96 children and young people were recruited to the study. Methodology Baseline data In order to make comparisons between relevant variables and glucose levels, the following baseline data will be collected from the dietitians and sent to the chief investigator, along with the artificial identifier on the Excel spreadsheet as discussed earlier at the stage of recruitment of participants: Parent's email address Sex, date of birth and recent weight and height (for calculation of BMI and BMI centile) and date of when this was taken Date of diagnosis of T1D Last four HbA1c Total daily insulin dose (TDD) Insulin: carbohydrate ratios (ICR) and Insulin Sensitivity Factor (ISF) Current insulin regimen - including the type of insulin prescribed and if applicable type of insulin pump i.e. open or closed loop system. Run-in period At recruitment the dietitians will be asked to arrange a review of the participants insulin regimen including the insulin to carbohydrate ratio's (ICR), insulin sensitivity factor (ISF) and basal background insulin doses/rates. The dietitian will be asked to inform the chief investigator when this has taken place. Participants will be asked to commence the test meals following this. Glucose measurement Data on interstitial glucose will be collected via Dexcom CGM. The Dexcom CGM data will be accessed by an NHS Highland research 'Clarity Clinic' with Dexcom CLARITY® Clinic Portal (Dexcom In, San Diego, California (CA), USA). The chief investigator is administrator of this clinic. Once the managing dietitian has obtained each participant's consent, the participant's parent's email address will be sent to the chief investigator along with the baseline information/data as described above. The chief investigator, as administrator of the Clarity Clinic account, will then invite the participant, via email, to be added to the clinic. Once the invite has been accepted, it will stand for the period of the recording i.e. until all the test meals and questionnaires have been completed. Once the participant has submitted their last questionnaire, they will be removed from the Dexcom CLARITY® Clinic Portal. Following the provision of CGM data and review of the insulin regimen by the diabetes team, participants will be randomised to test each of the three test meals on two separate occasions with a control meal (usual breakfast meal) for each test meal. Randomisation will be achieved using a Latin square randomisation. The tool used for this will be http://www.jerrydallal.com/random/randomize.htm. Randomisation will be done in a block of four. The test meals are based on foods children and young people enjoy eating. There are three meals. Test meal one includes a high glycaemic index cereal meal with milk and has a high glycaemic load (> 20), test meal two is the same cereal meal with a high glycaemic load (>20) with addition of 10g protein and test meal three has a medium glycaemic load (10-20). For test meals one and two there are three portion size options to meet age appropriate requirements and appetites. The participants will be able to choose from two different cereals for test meal 1 and a choice of protein sources for test meal 2. They will be asked to keep to the same choice of cereal and protein source for the repeat meal. They will be asked to consume at least 75% of the meal to ensure the threshold of the glycaemic load is met. The instructions and details of the test meals are presented in Appendix 11. The control meals will be the participant's usual breakfast of choice. Participants will be asked to follow their usual insulin regimen as advised by their diabetes team i.e. their usual insulin dose and dose timing. For both test and control meals participants will be asked to avoid any further food intake during three-hour postprandial period other than carbohydrate adjustments required to treat any hypoglycaemia. Participants will also be asked to avoid drinks except water or carbohydrate free juices. They will also be asked to avoid physical activity of more than 30 minutes in duration. To minimise disruption to their normal daily activities, they will be advised to test the meal on a day when there is no planned physical activity i.e. a school day with no morning physical education. The CGM data will be collected throughout this time as discussed above. Postprandial Questionnaire The participants will be asked to complete a postprandial questionnaire using 'online survey'. This includes questions about the meal and the three-hour postprandial period. The questionnaire is presented in Appendix 10. They will be asked to wait a minimum of three hours before answering and submitting the questionnaire. They will be encouraged to complete it on the same day as the test or control meal. Data analysis This will be a mix of univariate, bivariate and multivariate analysis as this is best suited to describing, summarising and visualising these data. Outputs will include the distribution of glucose levels post-breakfast to determine the spread and dispersion of the data.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
type1diabetes

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Participants will be randomised to test each of the three test meals on two separate occasions with a control meal (usual breakfast meal) for each test meal. Randomisation will be achieved using a Latin square randomisation. The tool used for this will be http://www.jerrydallal.com/random/randomize.htm. Randomisation will be done in a block of four.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Test meal 1
Arm Type
Other
Arm Description
High glycaemic load breakfast meal
Arm Title
Test meal 2
Arm Type
Other
Arm Description
High glycaemic lead with additional 10g protein breakfast meal
Arm Title
Test meal 3
Arm Type
Other
Arm Description
Medium glycaemic load breakfast meal
Intervention Type
Other
Intervention Name(s)
High glycaemic load breakfast meal
Intervention Description
Breakfast meal
Intervention Type
Other
Intervention Name(s)
High glycaemic load breakfast meal with additional 10g protein
Intervention Description
Breakfast meal
Intervention Type
Other
Intervention Name(s)
Medium glycaemic load breakfast meal
Intervention Description
Breakfast meal
Primary Outcome Measure Information:
Title
Mean glucose (mmol/l)
Description
mmol/l
Time Frame
three-hour postprandial breakfast period
Secondary Outcome Measure Information:
Title
Mean peak glucose
Description
mmol/l
Time Frame
three-hour postprandial breakfast period
Title
Mean time to peak
Description
minutes
Time Frame
three-hour postprandial breakfast period
Title
Mean time to recover
Description
minutes
Time Frame
three-hour postprandial breakfast period
Title
Area under the glucose curve
Description
mmol/minute
Time Frame
three-hour postprandial breakfast period
Title
Range times (Time in range, time above range, time below range)
Description
Percentage
Time Frame
three-hour postprandial breakfast period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children and young people aged between 5-17 years Diagnosis of type 1 diabetes for a minimum of one year On multiple daily injections (MDI) together with carbohydrate counting or Continuous Subcutaneous Insulin Infusion (CSII) using either open or closed loop systems. Use Dexcom continuous glucose monitoring (CGM) on a regular basis Have a Dexcom Clarity account and use the Clarity App Regularly eats a breakfast meal before midday Access to internet and email Exclusion Criteria: Prescribed anti-hyperglycaemia agents i.e. Glucophage (Metformin) and or antidepressants. Any other medical conditions that may impact on the digestion and or absorption of nutrients, including coeliac disease and gastroparesis. Vegans Allergic or intolerant to the test meals Experiencing difficulties with food including diagnosed eating disorders Currently actively taking part in another research study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julie Johnson, MNutr
Organizational Affiliation
University of Stirling
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of Health Sciences and Sport
City
Stirling
State/Province
Stirlingshire
ZIP/Postal Code
FK9 4LA
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
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