search
Back to results

Remote Monitoring of Diabetes in Pregnancy: a Feasibility Study (Tele-Mum)

Primary Purpose

Gestational Diabetes

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Telemonitoring
Control
Sponsored by
University of Ulster
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Gestational Diabetes focused on measuring Gestational diabetes, telemonitoring, telehealth, feasibility study

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant
  • Gestational Diabetes or IGT following an oral glucose tolerance test performed at the 24-28 week screening appointment
  • Able to use the telehealth equipment following training by staff from the company providing telehealth services
  • Have sufficient communication skills [hearing, speech & language] to be fully involved.
  • Willing to use one of the approved blood glucose meters for self monitoring of blood glucose, for the duration of the study.

Exclusion Criteria:

  • Previously diagnosed Type 1 diabetes or Type 2 diabetes as evidenced by medical records.
  • Other diagnosed medical problems or medical therapy such as steroid therapy that would influence blood glucose control and to be decided by the endocrinologist prior to recruitment. Such exclusions to be noted by the endocrinologist or diabetes nurse specialist.
  • Previous gestational diabetes is not an exclusion criterion.

Sites / Locations

  • Letterkenny General Hospital
  • Altnagelvin Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Telemonitoring

Control group

Arm Description

The telemonitoring group will receive usual care but be asked to download their blood sugar readings and take a blood pressure and weight measurement each week. This will be reviewed by their diabetes health care team to assess the possibility of replacing alternate anti-natal/diabetes clinics with telemonitoring review in a future study. Acceptability to staff and patients will be assessed through a questionnaire (patients only) and qualitative interviews.

Control group will consist of usual care and review at clinic.

Outcomes

Primary Outcome Measures

Patient satisfaction
The previously validated 'Telemedicine satisfaction and usefulness questionnaire' will be used to assess patient satisfaction with the telemonitoring service. Qualitative interviews exploring the patient experience of telemonitoring will also be carried out and then analysed using the framework approach. An adapted version of this questionnaire looking specifically at the use of a blood glucose meter will be given to the control group.
Health care staff satisfaction
The professionals involved in caring for the women using remote telemonitoring technology in antenatal or diabetes clinics will be invited to take part in a focus group at each site. If it is not possible to arrange a time and place suitable for staff in order to hold a focus group it may be necessary to hold one to one structured interviews with staff. The questions used in the focus group will aim to assess the acceptability of telemonitoring to health care staff who use it.
Management decision comparison
Weighted kappa will be used to meaure the level of agreement in between clinic and telemonitoring review management decisions (in excess of the amount of agreement that we would expected by chance). This will allow the determination of inter-rater, intra-rater and inter-institutional agreement between clinic and telemonitoring review management decisions.

Secondary Outcome Measures

HbA1c
HbA1c mmol/l and IFCC units
Mean fasting blood glucose
mmol/l plasma glucose
Blood pressure
mmHg
Gestational age at delivery
Gestational age in weeks at delivery
Type of delivery
Vaginal or Caesarean section
Pre-eclampsia
Presence or absence of any pre-eclampsia
Documented problems with pregnancy
Presence of any documented problems during pregnancy
Weight of baby
Weight in kg
Apgar score
Apgar score at one and five minutes (out of 10)
Admission to neonatal unit
Whether the baby needed admission to the neonatal unit
Respiratory distress
Presence of any episodes of documented Respiratory distress in first 24 hours of life
Jaundice
Presence of any jaundice in first 24 hours of life
Neonatal hypoglycaemia
Presence of any documented episodes of neonatal hypoglycaemia in first 24 hours of life
Shoulder dystocia
Presence of any shoulder dystocia
Malformations
Any malformations at delivery
Post-prandial blood glucose
mmol/l plasma glcuose
Length of baby
centimeters
Macrosomia
Presence or absence of macrosomia
Head circumference
centimeters
Average number of monitoring episodes per day
Average number of monitoring episodes per day
Number of downloads missed
Number of downloads missed by those in the telemonitoring group

Full Information

First Posted
June 22, 2012
Last Updated
January 24, 2014
Sponsor
University of Ulster
Collaborators
Western Health and Social Care Trust, Letterkenny General Hospital, University College Hospital Galway
search

1. Study Identification

Unique Protocol Identification Number
NCT01630759
Brief Title
Remote Monitoring of Diabetes in Pregnancy: a Feasibility Study
Acronym
Tele-Mum
Official Title
Remote Monitoring of Diabetes in Pregnancy: a Feasibility Study for a Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
March 2013 (Actual)
Study Completion Date
May 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Ulster
Collaborators
Western Health and Social Care Trust, Letterkenny General Hospital, University College Hospital Galway

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
When women with diabetes become pregnant it is particularly important to control blood sugar levels to prevent complications. Women are advised to test their blood glucose levels seven times a day and to attend antenatal and diabetes clinics every 1-2 weeks throughout the pregnancy. For those living in rural areas in the North and West of Ireland getting to a hospital specialising in the management of diabetes and pregnancy on such a regular basis can be a challenge. Telemonitoring provides a possible solution to this problem by allowing patients to monitor their vital signs at home and transmit the information via telephone to their healthcare provider. If women could be safely monitored remotely for every other appointment it would mean that they would only need to visit the hospital once a month on a routine basis but with the option of attending the hospital if the remote telemonitoring indicated that this were necessary. The aim of this study is to assess the feasibility and the acceptability of using remote telemonitoring facilities between antenatal women with gestational diabetes and the diabetes team and the possibility of replacing alternate diabetic review clinics with remote telemonitoring. In addition this study will explore the feasibility of running a full randomised control trial of this topic. Women will be asked to monitor their blood sugar levels seven times a day which is part of usual care. However those in the remote telemonitoring group will be asked to measure their blood sugar using a meter that can transmit the results via a telephone line and to transmit them weekly. They will also be asked to measure their blood pressure and weight weekly and to download these results weekly for a health care professional to review. These results will be reviewed on a weekly basis by a health care professional who will contact the patient if necessary to discuss the results. Women will be followed-up from the date of diagnosis through to delivery. Both staff and patients will be asked to give their views on the safety and acceptability of remote telemonitoring through questionnaires, focus groups or interviews. The management decisions made on reviewing the intervention group in clinic and reviewing remote telemonitoring results will also be recorded. In order for remote telemonitoring to be a viable replacement for clinic review it must allow health care professionals to make comparable management decisions. Clinical data will be collected in order to provide descriptive statistics for those who take part and to ensure that this information could be collected in any future Randomised Control Trial (RCT) looking at this topic.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes
Keywords
Gestational diabetes, telemonitoring, telehealth, feasibility study

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Telemonitoring
Arm Type
Experimental
Arm Description
The telemonitoring group will receive usual care but be asked to download their blood sugar readings and take a blood pressure and weight measurement each week. This will be reviewed by their diabetes health care team to assess the possibility of replacing alternate anti-natal/diabetes clinics with telemonitoring review in a future study. Acceptability to staff and patients will be assessed through a questionnaire (patients only) and qualitative interviews.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Control group will consist of usual care and review at clinic.
Intervention Type
Device
Intervention Name(s)
Telemonitoring
Intervention Description
Use of telemonitoring facilities to monitor weight, blood pressure and blood sugar during pregnancy complicated by gestational diabetes
Intervention Type
Other
Intervention Name(s)
Control
Other Intervention Name(s)
Usual care
Intervention Description
The control group will receive usual diabetes/antinatal care. The outcomes from usual care will be compared with the outcomes from the telemonitoring group in order to ensure that it provides comparable care.
Primary Outcome Measure Information:
Title
Patient satisfaction
Description
The previously validated 'Telemedicine satisfaction and usefulness questionnaire' will be used to assess patient satisfaction with the telemonitoring service. Qualitative interviews exploring the patient experience of telemonitoring will also be carried out and then analysed using the framework approach. An adapted version of this questionnaire looking specifically at the use of a blood glucose meter will be given to the control group.
Time Frame
At 36-39 weeks gestation
Title
Health care staff satisfaction
Description
The professionals involved in caring for the women using remote telemonitoring technology in antenatal or diabetes clinics will be invited to take part in a focus group at each site. If it is not possible to arrange a time and place suitable for staff in order to hold a focus group it may be necessary to hold one to one structured interviews with staff. The questions used in the focus group will aim to assess the acceptability of telemonitoring to health care staff who use it.
Time Frame
At completion of the study estimated to be January 2013
Title
Management decision comparison
Description
Weighted kappa will be used to meaure the level of agreement in between clinic and telemonitoring review management decisions (in excess of the amount of agreement that we would expected by chance). This will allow the determination of inter-rater, intra-rater and inter-institutional agreement between clinic and telemonitoring review management decisions.
Time Frame
At weekly clinic or telemonitoring review from time recruited into study to delivery, estimated at an average of twelve weeks.
Secondary Outcome Measure Information:
Title
HbA1c
Description
HbA1c mmol/l and IFCC units
Time Frame
Monthly for duration of participation in study, estimated at 2-3 months
Title
Mean fasting blood glucose
Description
mmol/l plasma glucose
Time Frame
Weekly for duration of participation in study, estimated at 12 weeks
Title
Blood pressure
Description
mmHg
Time Frame
Weekly for duration of participation in study, estimated at 12 weeks
Title
Gestational age at delivery
Description
Gestational age in weeks at delivery
Time Frame
At delivery
Title
Type of delivery
Description
Vaginal or Caesarean section
Time Frame
At delivery
Title
Pre-eclampsia
Description
Presence or absence of any pre-eclampsia
Time Frame
At delivery
Title
Documented problems with pregnancy
Description
Presence of any documented problems during pregnancy
Time Frame
At delivery
Title
Weight of baby
Description
Weight in kg
Time Frame
At birth
Title
Apgar score
Description
Apgar score at one and five minutes (out of 10)
Time Frame
At birth
Title
Admission to neonatal unit
Description
Whether the baby needed admission to the neonatal unit
Time Frame
At one day after birth
Title
Respiratory distress
Description
Presence of any episodes of documented Respiratory distress in first 24 hours of life
Time Frame
At one day after birth
Title
Jaundice
Description
Presence of any jaundice in first 24 hours of life
Time Frame
At one day after birth
Title
Neonatal hypoglycaemia
Description
Presence of any documented episodes of neonatal hypoglycaemia in first 24 hours of life
Time Frame
At one day after birth
Title
Shoulder dystocia
Description
Presence of any shoulder dystocia
Time Frame
At birth
Title
Malformations
Description
Any malformations at delivery
Time Frame
At delivery
Title
Post-prandial blood glucose
Description
mmol/l plasma glcuose
Time Frame
Weekly for duration of participation in study, estimated at 12 weeks
Title
Length of baby
Description
centimeters
Time Frame
At birth
Title
Macrosomia
Description
Presence or absence of macrosomia
Time Frame
At birth
Title
Head circumference
Description
centimeters
Time Frame
At birth
Title
Average number of monitoring episodes per day
Description
Average number of monitoring episodes per day
Time Frame
At delivery
Title
Number of downloads missed
Description
Number of downloads missed by those in the telemonitoring group
Time Frame
At delivery

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant Gestational Diabetes or IGT following an oral glucose tolerance test performed at the 24-28 week screening appointment Able to use the telehealth equipment following training by staff from the company providing telehealth services Have sufficient communication skills [hearing, speech & language] to be fully involved. Willing to use one of the approved blood glucose meters for self monitoring of blood glucose, for the duration of the study. Exclusion Criteria: Previously diagnosed Type 1 diabetes or Type 2 diabetes as evidenced by medical records. Other diagnosed medical problems or medical therapy such as steroid therapy that would influence blood glucose control and to be decided by the endocrinologist prior to recruitment. Such exclusions to be noted by the endocrinologist or diabetes nurse specialist. Previous gestational diabetes is not an exclusion criterion.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vivien E Coates, PhD
Organizational Affiliation
University of Ulster
Official's Role
Principal Investigator
Facility Information:
Facility Name
Letterkenny General Hospital
City
Letterkenny
State/Province
Donegal
Country
Ireland
Facility Name
Altnagelvin Hospital
City
Londonderry
ZIP/Postal Code
BT47 6SB
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
26394017
Citation
Given JE, Bunting BP, O'Kane MJ, Dunne F, Coates VE. Tele-Mum: A Feasibility Study for a Randomized Controlled Trial Exploring the Potential for Telemedicine in the Diabetes Care of Those with Gestational Diabetes. Diabetes Technol Ther. 2015 Dec;17(12):880-8. doi: 10.1089/dia.2015.0147. Epub 2015 Sep 22.
Results Reference
derived

Learn more about this trial

Remote Monitoring of Diabetes in Pregnancy: a Feasibility Study

We'll reach out to this number within 24 hrs