Gestational Diabetes Clinical Trial
Official title:
Remote Monitoring of Diabetes in Pregnancy: a Feasibility Study for a Randomised Controlled Trial
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.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research
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