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Clinical Trials/NCT02783612
NCT02783612UnknownNot Applicable

Improvement of Compliance by Digital Blood Glucose Monitoring of Women With Gestational Diabetes

Wolfson Medical Center1 site in 1 country100 target enrollmentStarted: March 1, 2016Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
100
Locations
1
Primary Endpoint
Assessing the compliance of the research group compared to the control group.

Study Overview

Brief Summary

Assessing blood glucose control in women with gestational diabetes can be challenging. The standard of care remains visual inspection of blood glucose paper diaries of self-performed capillary monitoring during regular meeting in High Risk pregnancy clinics.

The researchers are interested in preforming a randomized control trial comparing women with the diagnosis of gestational diabetes with regular High-Risk clinic surveillance to digital monitoring using an application in a Smart-phone and submitting those values via email in addition to the regular clinic appointments.

The Primary outcome of the trial is to assess the compliance of the research group as compared to the control group.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 45 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •gestational diabetes

Exclusion Criteria

  • •pre-gestational diabetes

Arms & Interventions

glucose application

Experimental

Regular high risk pregnancy clinic surveillance in addition to a Smart phone application for registering the Blood glucose levels and submitting via email every 3-5 days to the High risk Doctor involved in the trial.

Intervention: glucose buddy application (Other)

Regular monitoring

No Intervention

Regular high risk pregnancy clinic surveillance

Outcomes

Primary Outcomes

Assessing the compliance of the research group compared to the control group.

Time Frame: 18 month

By calculating the amount of daily glucose measurements in the research group compared to the number of glucose measurements in the control group

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (1)

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