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Trial of Remote Evaluation and Treatment of Gestational Diabetes Mellitus (TREAT-GDM)

Primary Purpose

Gestational Diabetes Mellitus, Pregnancy

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Blue tooth enabled glucose meter with smart phone application
Self home blood glucose monitoring
Sponsored by
University of Oxford
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Gestational Diabetes Mellitus focused on measuring Gestational diabetes mellitus, m Health, Smartphone, Blood glucose monitoring

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women with an abnormal 75 gram 2 hour glucose tolerance test as defined by the IADPSG (International Association of Diabetes in Pregnancy Study Group)
  • Willingness and able to give informed consent
  • Female aged between 18-40 years
  • Singleton pregnancy
  • Able to travel to hospital independently

Exclusion Criteria:

  • Impaired cognitive function such that she is unable to operate m-health equipment
  • Any evidence of fetal compromise
  • Known risk factors for obstetric complications, other than obesity and diabetes
  • Gestational diabetes requiring immediate pharmacologic treatment
  • Twins or higher order pregnancy
  • OGTT (Oral Glucose Tolerance Test) suggesting preexisting diabetes (fasting blood glucose >= 7.0 or 2 hour >= 11.1 mmol/L
  • Gestation greater than 34+6 at the time of potential recruitment
  • Unable to speak English well enough to explain or use equipment

Sites / Locations

  • John Radcliffe Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Smart phone app glucose monitoring

Standard glucose monitoring

Arm Description

Home blood glucose monitoring results directly transmitted via a bluetooth enabled smart phone app to a central database to be reviewed by clinicians

Home blood glucose monitoring results recorded by hand in a paper diary by the patient and reviewed by the clinical team in the outpatient clinic.

Outcomes

Primary Outcome Measures

Glycosylated haemogloblin
Glycosylated haemoglobin (HbA1C) will be measured at the time of recruitment (around 28 weeks gestation) and at 36 weeks gestation. This will be approximately 8 weeks after recruitment (time 0).

Secondary Outcome Measures

Mean Blood glucose levels for fasting, pre-prandial and post-prandial readings
Mean blood glucose levels for all readings measured fasting, pre-prandial and post prandial will be calculated over the 10 week participation in the trial (from recruitment at 28 weeks gestation to delivery at 38 weeks gestation).
Percentage of 'on target' blood glucose readings
Fasting readings as defined >=3.5 and <=5.8 mmol/L and post prandial readings >= 3.5 and <= 7.7 mmol/L for the first four weeks after randomisation and the second four weeks after randomisation
Effectiveness of monitoring
Time to first trigger point (intensive dietary and lifestyle advice and increase monitoring to 7 days home per week) Time to second trigger point (insulin or metformin therapy) Time to treatment Number of changes to hypoglycaemics Maximum dose of insulin and metformin
Maternal outcomes
Perineal trauma (defined as third or fourth degree tear), pregnancy induced hypertension and preeclampsia, admission to higher level of care for mother. This will be measured up to 7 days post delivery (if birth is at 38 weeks, this will be 11 weeks after trial recruitment, unless birth occurs earlier)
Maternal weight gain,
Weight gain in kilograms from trial recruitment until last antenatal visit prior to delivery
Birthweight
Z score of weight in kilograms for gestational age at delivery and Birthweight greater than 4.5kg
Birth injury
Fracture of clavicle or humerus or other injury attributed to difficult birth, such as Erbs palsy or skull fracture
Neonatal hypoglycaemia
Documented blood glucose level <2.5mmol/L or requiring parenteral feeding within the first 48 hours of life after birth at around 38 weeks gestation (birth at approximately 10 weeks following trial recruitment and blood glucose monitoring in the neonate up to 48 hours after this)

Full Information

First Posted
July 4, 2013
Last Updated
May 19, 2016
Sponsor
University of Oxford
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1. Study Identification

Unique Protocol Identification Number
NCT01916694
Brief Title
Trial of Remote Evaluation and Treatment of Gestational Diabetes Mellitus
Acronym
TREAT-GDM
Official Title
A Randomised Pilot Trial to Compare Remote Blood Glucose Monitoring With Standard Clinical Care in the Gestational Diabetic Population
Study Type
Interventional

2. Study Status

Record Verification Date
May 2016
Overall Recruitment Status
Completed
Study Start Date
September 2013 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
February 2016 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Diabetes in pregnancy (gestational diabetes) is becoming more common. It can lead to problems for both mothers-to-be and their babies such as causing a large baby and difficult birth. Gestational diabetes in the mother may also lead to effects on the long term health of the baby. Most people today use mobile phones. Our research is looking at using a mobile phone app to help with diabetes care in pregnancy. In particular, the investigators are using phones which connect to the standard blood glucose monitoring machines given to all women with gestational diabetes to see if sending the hospital team blood test results between clinic appointments can result in the need for fewer clinic visits. The investigators are also testing to see how acceptable using mobile phones in this way, is to our patients and that the control of the blood glucose and outcomes for the mother and baby are at least as good as standard care. The investigators are planning to recruit 200 women who receive care for their gestational diabetes at the Oxford University Hospitals NHS (National Health Service) Trust. They will be randomised so that 100 will receive standard care, and 100 will have a mobile phone "app" linked to the blood glucose machines to send blood glucose readings directly to the diabetes care team to review. Both groups will be asked to test their blood glucose levels at home regularly with a glucometer. All participants will also be given lifestyle advice to reduce the chance they will need medication. Blood glucose control will be measured also by the percentage of glycated hemoglobin (HbA1c) at the time of diagnosis of gestational diabetes and before delivery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes Mellitus, Pregnancy
Keywords
Gestational diabetes mellitus, m Health, Smartphone, Blood glucose monitoring

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
203 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Smart phone app glucose monitoring
Arm Type
Experimental
Arm Description
Home blood glucose monitoring results directly transmitted via a bluetooth enabled smart phone app to a central database to be reviewed by clinicians
Arm Title
Standard glucose monitoring
Arm Type
Active Comparator
Arm Description
Home blood glucose monitoring results recorded by hand in a paper diary by the patient and reviewed by the clinical team in the outpatient clinic.
Intervention Type
Device
Intervention Name(s)
Blue tooth enabled glucose meter with smart phone application
Intervention Type
Behavioral
Intervention Name(s)
Self home blood glucose monitoring
Intervention Description
Fingerprick testing of blood glucose levels before and 2 hours after meals
Primary Outcome Measure Information:
Title
Glycosylated haemogloblin
Description
Glycosylated haemoglobin (HbA1C) will be measured at the time of recruitment (around 28 weeks gestation) and at 36 weeks gestation. This will be approximately 8 weeks after recruitment (time 0).
Time Frame
8 weeks from recruitment at 28 weeks gestation to 36 weeks gestation
Secondary Outcome Measure Information:
Title
Mean Blood glucose levels for fasting, pre-prandial and post-prandial readings
Description
Mean blood glucose levels for all readings measured fasting, pre-prandial and post prandial will be calculated over the 10 week participation in the trial (from recruitment at 28 weeks gestation to delivery at 38 weeks gestation).
Time Frame
10 weeks (from 28 weeks gestation to 38 weeks gestation)
Title
Percentage of 'on target' blood glucose readings
Description
Fasting readings as defined >=3.5 and <=5.8 mmol/L and post prandial readings >= 3.5 and <= 7.7 mmol/L for the first four weeks after randomisation and the second four weeks after randomisation
Time Frame
8 weeks (from recruitment at 28 weeks gestation to 36 weeks gestation)
Title
Effectiveness of monitoring
Description
Time to first trigger point (intensive dietary and lifestyle advice and increase monitoring to 7 days home per week) Time to second trigger point (insulin or metformin therapy) Time to treatment Number of changes to hypoglycaemics Maximum dose of insulin and metformin
Time Frame
10 weeks (from 28 weeks gestation to 38 weeks gestation)
Title
Maternal outcomes
Description
Perineal trauma (defined as third or fourth degree tear), pregnancy induced hypertension and preeclampsia, admission to higher level of care for mother. This will be measured up to 7 days post delivery (if birth is at 38 weeks, this will be 11 weeks after trial recruitment, unless birth occurs earlier)
Time Frame
Approximately 11 weeks after recruitment
Title
Maternal weight gain,
Description
Weight gain in kilograms from trial recruitment until last antenatal visit prior to delivery
Time Frame
10 weeks (from 28 weeks gestation to 38 weeks gestation)
Title
Birthweight
Description
Z score of weight in kilograms for gestational age at delivery and Birthweight greater than 4.5kg
Time Frame
At birth (approximately 10 weeks after trial recruitment)
Title
Birth injury
Description
Fracture of clavicle or humerus or other injury attributed to difficult birth, such as Erbs palsy or skull fracture
Time Frame
At birth (approximately 10 weeks after trial recruitment)
Title
Neonatal hypoglycaemia
Description
Documented blood glucose level <2.5mmol/L or requiring parenteral feeding within the first 48 hours of life after birth at around 38 weeks gestation (birth at approximately 10 weeks following trial recruitment and blood glucose monitoring in the neonate up to 48 hours after this)
Time Frame
Approximately 10.5 weeks after recruitment
Other Pre-specified Outcome Measures:
Title
Economic evaluation
Description
Direct cost of clinical care provision including outpatient appointments, emergency presentations, inpatient admission nights, neonatal intensive and special care admission nights, cost of phone and blue tooth equipment, time spent on computer system by clinical staff, other associated treatment and obstetric management costs, costs associated with co-morbid conditions
Time Frame
11 weeks from trial recruitment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women with an abnormal 75 gram 2 hour glucose tolerance test as defined by the IADPSG (International Association of Diabetes in Pregnancy Study Group) Willingness and able to give informed consent Female aged between 18-40 years Singleton pregnancy Able to travel to hospital independently Exclusion Criteria: Impaired cognitive function such that she is unable to operate m-health equipment Any evidence of fetal compromise Known risk factors for obstetric complications, other than obesity and diabetes Gestational diabetes requiring immediate pharmacologic treatment Twins or higher order pregnancy OGTT (Oral Glucose Tolerance Test) suggesting preexisting diabetes (fasting blood glucose >= 7.0 or 2 hour >= 11.1 mmol/L Gestation greater than 34+6 at the time of potential recruitment Unable to speak English well enough to explain or use equipment
Facility Information:
Facility Name
John Radcliffe Hospital
City
Oxford
State/Province
Oxfordshire
ZIP/Postal Code
OX3 9DU
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
29559428
Citation
Mackillop L, Hirst JE, Bartlett KJ, Birks JS, Clifton L, Farmer AJ, Gibson O, Kenworthy Y, Levy JC, Loerup L, Rivero-Arias O, Ming WK, Velardo C, Tarassenko L. Comparing the Efficacy of a Mobile Phone-Based Blood Glucose Management System With Standard Clinic Care in Women With Gestational Diabetes: Randomized Controlled Trial. JMIR Mhealth Uhealth. 2018 Mar 20;6(3):e71. doi: 10.2196/mhealth.9512.
Results Reference
derived
PubMed Identifier
26988348
Citation
Mackillop LH, Bartlett K, Birks J, Farmer AJ, Gibson OJ, Kevat DA, Kenworthy Y, Levy JC, Loerup L, Tarassenko L, Velardo C, Hirst JE. Trial protocol to compare the efficacy of a smartphone-based blood glucose management system with standard clinic care in the gestational diabetic population. BMJ Open. 2016 Mar 17;6(3):e009702. doi: 10.1136/bmjopen-2015-009702.
Results Reference
derived
PubMed Identifier
25361643
Citation
Hirst JE, Mackillop L, Loerup L, Kevat DA, Bartlett K, Gibson O, Kenworthy Y, Levy JC, Tarassenko L, Farmer A. Acceptability and user satisfaction of a smartphone-based, interactive blood glucose management system in women with gestational diabetes mellitus. J Diabetes Sci Technol. 2015 Jan;9(1):111-5. doi: 10.1177/1932296814556506. Epub 2014 Oct 30.
Results Reference
derived

Learn more about this trial

Trial of Remote Evaluation and Treatment of Gestational Diabetes Mellitus

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