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Trial registered on ANZCTR
Registration number
ACTRN12614001198617
Ethics application status
Approved
Date submitted
4/11/2014
Date registered
14/11/2014
Date last updated
15/01/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Insulin pump therapy for adolescents with type 1 diabetes and poor glycaemic control
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Scientific title
Insulin pump therapy (Medtronic Veo) for adolescents aged 14 to 18 years with type 1 diabetes and poor glycaemic control (HbA1c greater than 10% for the previous 6 months) , a 12 month pilot study investigating the effect on HbA1c.
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Secondary ID [1]
285592
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nil
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Universal Trial Number (UTN)
U1111-1163-6494
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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 1 diabetes
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Condition category
Condition code
Metabolic and Endocrine
293705
293705
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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
In this pilot interventional study, we will study patients with type 1 diabetes. They will recieve a 6 week education package on diabetes control and how to use an insulin pump. The education package will consisit of 4 x 2hour one on one sessions, three of which are with a diabetes nurse educator, and one with a dietician. The four sessions will be spread over 6 weeks and will occur at times that are convenient to the participant and health practitioner. They will be then started on an insulin pump and followed up for a period of 12 months.
We will use the Medtronic Veo insulin pump. This device delivers insulin in two ways: background basal insulin as a slow sub cutaneous infusion, and as bolus ammounts for carbohydrate that is eaten or to correct high blood glucose. The background basal rates and insulin bolus amounts are unique for each patient and are calculated by the team at pump start.
Participant compliance and progress will be monitored in their usual diabetes outpatient clinic by the paediatric endocrinologist.
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Intervention code [1]
290541
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Treatment: Devices
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Comparator / control treatment
Standard treamtent will be compared by identifying matched controls within our diabetes database. Standard treatment is continuing on regular injected insulin. At each clinic appointment (every 3 months, or sooner if the clinician deems this necessary) they have access to the diabetes consultant, dietician, social worker and diabetes nurse educator.
They will be matched by HbA1c, gender, age, and length of time with diabetes.
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Control group
Active
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Outcomes
Primary outcome [1]
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HbA1c. HbA1c is measured at every clinic appointment (every 3 months, or sooner if the clinically indicated), by a point of care DCA 1000 analyzer.
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Assessment method [1]
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Timepoint [1]
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12 months after starting insulin pump therapy
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Secondary outcome [1]
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Episodes of diabetic ketoacidosis requiring hospital admission. Diabetic ketoacidosis is defined as having a blood glucose of greater than 11mmol/L, a venous pH less than 7.3, and the presence of blood or urine ketones.
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Assessment method [1]
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Timepoint [1]
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Number of events over the 12 month study duration
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Secondary outcome [2]
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Sever hypoglycaemia, defined by an episode resulting in seizure or coma requiring help by a third party
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Assessment method [2]
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Timepoint [2]
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Number of events over the 12 month study duration
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Secondary outcome [3]
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Patient satisfaction using insulin pump therapy, assessed using the validated "pump satisfaction questionnaire"
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Assessment method [3]
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Timepoint [3]
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Assessed at the end of 12 months
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Secondary outcome [4]
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Fear of hypoglycaemia assessed by the University of Virginia hypoglycaemia fear survey for adolescents.
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Assessment method [4]
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Timepoint [4]
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Baseline and at 12 months
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Secondary outcome [5]
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Hypoglycaemia awareness assessed by the modified Clarke hypoglycaemia awareness questionnaire.
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Assessment method [5]
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Timepoint [5]
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Baseline and at 12 months
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Secondary outcome [6]
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Problem Areas in Diabetes (psychosocial) assessment), assessed by the Problem Areas in Diabetes Questionnaire (DAWN)
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Assessment method [6]
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Timepoint [6]
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Baseline and 12 months
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Secondary outcome [7]
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Quality of Life, assessed using the validated PedsQL diabetes module Version 3.0
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Assessment method [7]
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Timepoint [7]
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Baseline and at 12 months
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Eligibility
Key inclusion criteria
1. Age 14 - 18 years with type 1 diabetes
2. Duration of diabetes at least 12 months
3. Insulin pump therapy naive
4. HbA1C>10% for the preceding 6 months
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Minimum age
14
Years
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Maximum age
18
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
1. Pregnancy
2. Any additional condition(s) that in the investigator’s opinion would warrant exclusion from the study or prevent the subject from completing the study
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Patients currently being seen by the Princess Margaret Hospital diabetes and Endocrinology team who are aged 14 - 18 years and have an HbA1c of greater than 10% for the previous 6 months will be identified through our patient database.
Eligible patients will be offerred entry into the trial, and will be accepted in a first come first serve basis.
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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
This is a pilot study. Should we show improvement in glycaemia in the 12 month period we envisage designing an in clinic program that can be assessed prospectively in the future.
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Phase
Phase 4
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Type of endpoint/s
Safety/efficacy
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Statistical methods / analysis
Study participants will be matched 2:1 with active patients in our database (matched for HbA1c, age, and length of diabetes). We will use a student’s t test (2 tailed).
10 patients will be enrolled. This is assuming a mean baseline HbA1c of 11%, and a mean reduction of 1.5%, with an SD of 1.3%(see ref). This is based on a power calculation of 80%
REF: Johnson SR, Cooper MN, Jones TW, Davis EA. Long-term outcome of insulin pump therapy in children with type 1 diabetes assessed in a large population-based case–control study. Diabetologia. 2013;56(11):2392-400.
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/02/2015
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Actual
14/05/2015
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Date of last participant enrolment
Anticipated
1/04/2015
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Actual
29/08/2015
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
10
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Accrual to date
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Final
10
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Princess Margaret Hospital - Subiaco
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Recruitment postcode(s) [1]
8863
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6008 - Subiaco
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Funding & Sponsors
Funding source category [1]
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Charities/Societies/Foundations
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Name [1]
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Princess Margaret Hospital Foundation
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Address [1]
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GPO box D184, Perth WA 6008
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Martin de Bock
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Address
Princess Margaret Hospital
Roberts Road
Subiaco
Perth 6008
Western Australia
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Elizabeth Davis
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Address [1]
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Princess Margaret Hospital
Roberts Road
Subiaco
Perth 6008
Western Australia
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Country [1]
288897
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Princess Margaret Hospital Ethics Committee
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Ethics committee address [1]
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GPO box D184 Perth WA 6840
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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15/10/2014
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Approval date [1]
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20/11/2014
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Ethics approval number [1]
291895
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Summary
Brief summary
The study will let us explore the role of insulin pump therapy for adolescent with type 1 diabetes and poor control. These patients are often excluded from accessing this therapeutic tools due to concerns regarding safety, or because a lack of financial support. We will look at many outcomes including glycaemic control, episodes of diabetic ketoacidosis and severe hypoglycaemia, as well general quality of life and psychosocial functioning.
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Trial website
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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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Dr Martin de Bock
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Address
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Princess Margaret Hospital Roberts Road
Subiaco
Perth WA 6008
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Country
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Australia
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Phone
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+61 8 93407915
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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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Martin de Bock
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Address
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Princess Margaret Hospital Roberts Road
Subiaco
Perth WA 6008
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Country
52483
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Australia
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Phone
52483
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+61 8 93407915
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Fax
52483
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Email
52483
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[email protected]
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Contact person for scientific queries
Name
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Martin de Bock
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Address
52484
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Princess Margaret Hospital Roberts Road
Subiaco
Perth WA 6008
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Country
52484
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Australia
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Phone
52484
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+61 8 93407915
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Fax
52484
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Email
52484
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[email protected]
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No information has been provided regarding IPD availability
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
Source
Title
Year of Publication
DOI
Dimensions AI
Insulin Pump Therapy in Adolescents With Very Poor Glycemic Control During a 12-Month Cohort Trial
2018
https://doi.org/10.1177/1932296818769338
N.B. These documents automatically identified may not have been verified by the study sponsor.
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