telemedicine ,pregnant women with gestational diabetes mellitus efficacy, Target-controlled, Maternal outcomes ,telemedicine
Conditions
Interventions
Patients received normal care. come to see the doctor by appointment,Those who randomly get an experimental group
-Must be able to receive at least 6-12 consultations
- send blood sugar information vi
No Intervention Other,Experimental Other
Group C,Group T
Sponsors
None listed
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Age 18 years to 45 years 2.single pregnant woman 3. GDM is diagnosed by the 100g Oral Glucose Tolerance Test OGTT. 4. Availability of devices such as smartphones, tablets, computers with webcams. 5. Availability of email and stable internet connection. 6.Need help/support participating via video call 7. Can record blood sugar level values
Exclusion criteria
Exclusion criteria: 1. Refusing to participate in a research study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average Blood Sugar Level Average fasting blood sugar (FBS) level every 1 week from entering the project until giving birth mg/dL,Postprandrial (2hr PP) every week from entering the project until giving birth. mg/dL | — |
Secondary
| Measure | Time frame |
|---|---|
| gestational age Gestational age at delivery in weeks week | — |
Countries
Thailand
Contacts
Public ContactRathawit Suntorn
Nongkhai Hospital
Outcome results
None listed