Advanced Bolus Calculator for Type 1 Diabetes (ABC4D) (ABC4D)
Primary Purpose
Type 1 Diabetes
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
ABC4D
Novorapid
Sponsored by
About this trial
This is an interventional other trial for Type 1 Diabetes focused on measuring Type 1 Diabetes, Advanced Bolus Calculator
Eligibility Criteria
Inclusion Criteria:
- Adults ≥18 years of age
- Diagnosis of T1DM for > 1 year
- On MDI using a basal-bolus insulin regime
- Structured education in previous 3 years
- HbA1c ≤ 86mmol/mol
- No severe hypoglycaemia (defined as needing 3rd party assistance) in previous year
Exclusion Criteria:
- Recurrent severe hypoglycaemia
- Pregnant or planning pregnancy
- Breastfeeding
- Enrolled in other clinical trials
- Have active malignancy or under investigation for malignancy
- Addison's Disease
- Gastroparesis
- Autonomic neuropathy
- Concomitant use of GLP-1 analogues and gliptins
- Visual impairment
- Reduced manual dexterity
Sites / Locations
- Imperial College London, Imperial College Healthcare NHS Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
MDI of insulin & ABC4D
MDI of insulin
Arm Description
Advanced Bolus Calculator for Type Diabetes (ABC4D)
Multiple daily injections(MDI) of insulin
Outcomes
Primary Outcome Measures
HbA1c
Glycaemic control
Post-prandial hypoglycaemia
Secondary Outcome Measures
Post-meal glucose at 60 and 120 minutes
Post-prandial area under the curve (AUC) at 120 minutes
Hypoglycaemia at 4-hours post-prandially
Glycaemic risk: LBGI and HBGI
Glycaemic variability: MAGE and CONGA-2
Change in weight (kg)
Number achieving target HbA1c ( ≤ 53 mmol/mol )
Full Information
NCT ID
NCT02053051
First Posted
January 22, 2014
Last Updated
March 29, 2022
Sponsor
Imperial College London
1. Study Identification
Unique Protocol Identification Number
NCT02053051
Brief Title
Advanced Bolus Calculator for Type 1 Diabetes (ABC4D)
Acronym
ABC4D
Official Title
Clinical Assessment of an Advanced Bolus Calculator for Type 1 Diabetes (ABC4D)
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
November 12, 2013 (Actual)
Primary Completion Date
September 30, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study aims to assess the safety and efficacy of a novel advanced bolus calculator in subjects with Type 1 diabetes. Insulin bolus calculators have been developed to aid insulin dose adjustment and existing standard insulin bolus calculator consist of a simple algorithm that requires five subject-specific parameters as input to generate a recommended bolus insulin dose:
current blood glucose (mmol/L)
target blood glucose (mmol/L)
insulin-to-carbohydrate ratio (grams of carbohydrate per 1 unit of insulin)
total grams of carbohydrate in meals
insulin sensitivity factor (reduction in glucose per 1 unit of insulin)
Detailed Description
The Diabetes Technology team at Imperial College have developed a novel advanced bolus calculator. The complete integrated system consists of a commercially available smartphone that holds the novel advanced algorithm. The system requires regular updates of cases derived from retrospective blinded continuous glucose monitoring data and for this a commercially available glucose sensor will be used. Each new case includes information about the problem (e.g. capillary blood glucose, meal information and physical exercise), solution (recommended insulin dose) and outcome (blood glucose following a meal). The novel decision support algorithm is based on case-based reasoning (CBR). CBR is an artificial intelligence technique that tries to solve newly encountered problems by applying the solutions learned from solved problems encountered in the past.
The end-product is therefore a subject specific insulin bolus calculator that continues to improve with time. The project utilises commercially available glucose sensors and smartphones (iPhone), integrated with a novel algorithm for insulin bolus calculation. The aim of the ABC4D is to minimise high and low glucose excursions which are associated with the complications of diabetes including blindness, kidney failure, nerve damage and cardiovascular disease.
The clinical study has been designed to incrementally assess the device's ability to manage meal time insulin requirements at breakfast and lunch in a controlled supervised clinical environment over 8 hours (phase 1), followed by its use in the home environment over a 6 week period (phase 2) and finally over a 6 month period (phase 3).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes
Keywords
Type 1 Diabetes, Advanced Bolus Calculator
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MDI of insulin & ABC4D
Arm Type
Experimental
Arm Description
Advanced Bolus Calculator for Type Diabetes (ABC4D)
Arm Title
MDI of insulin
Arm Type
Active Comparator
Arm Description
Multiple daily injections(MDI) of insulin
Intervention Type
Device
Intervention Name(s)
ABC4D
Intervention Description
Advanced Bolus Calculator for Type 1 Diabetes (ABC4D) to calculate pre-meal insulin boluses
Intervention Type
Drug
Intervention Name(s)
Novorapid
Other Intervention Name(s)
Humalog
Intervention Description
Multiple daily injections(MDI) of insulin
Primary Outcome Measure Information:
Title
HbA1c
Description
Glycaemic control
Time Frame
6 months (phase 3 only)
Title
Post-prandial hypoglycaemia
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
Secondary Outcome Measure Information:
Title
Post-meal glucose at 60 and 120 minutes
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
Title
Post-prandial area under the curve (AUC) at 120 minutes
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
Title
Hypoglycaemia at 4-hours post-prandially
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
Title
Glycaemic risk: LBGI and HBGI
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
Title
Glycaemic variability: MAGE and CONGA-2
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
Title
Change in weight (kg)
Time Frame
6 months (phase 3 only)
Title
Number achieving target HbA1c ( ≤ 53 mmol/mol )
Time Frame
6 months (phase 3 only)
Other Pre-specified Outcome Measures:
Title
PAID score questionnaire
Description
Quality of life measure
Time Frame
6 months (Phase 3 only)
Title
Acceptability questionnaire (non-validated)
Description
Device acceptability assessment
Time Frame
For Phase 1 the time frame is 8 hours, for phase 2 it is 6 weeks and for phase 3 participants are followed-up for 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adults ≥18 years of age
Diagnosis of T1DM for > 1 year
On MDI using a basal-bolus insulin regime
Structured education in previous 3 years
HbA1c ≤ 86mmol/mol
No severe hypoglycaemia (defined as needing 3rd party assistance) in previous year
Exclusion Criteria:
Recurrent severe hypoglycaemia
Pregnant or planning pregnancy
Breastfeeding
Enrolled in other clinical trials
Have active malignancy or under investigation for malignancy
Addison's Disease
Gastroparesis
Autonomic neuropathy
Concomitant use of GLP-1 analogues and gliptins
Visual impairment
Reduced manual dexterity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Desmond Johnston, F.Med.Sci
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nick Oliver, MRCP
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Monika Reddy
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Imperial College London, Imperial College Healthcare NHS Trust
City
London
ZIP/Postal Code
W2 1PG
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
27196358
Citation
Reddy M, Pesl P, Xenou M, Toumazou C, Johnston D, Georgiou P, Herrero P, Oliver N. Clinical Safety and Feasibility of the Advanced Bolus Calculator for Type 1 Diabetes Based on Case-Based Reasoning: A 6-Week Nonrandomized Single-Arm Pilot Study. Diabetes Technol Ther. 2016 Aug;18(8):487-93. doi: 10.1089/dia.2015.0413. Epub 2016 May 19.
Results Reference
derived
Links:
URL
http://www3.imperial.ac.uk/bioinspiredtechnology/research/metabolic
Description
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Advanced Bolus Calculator for Type 1 Diabetes (ABC4D)
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