Mobile Instant Messaging-based Lifestyle Intervention for Gestational Diabetes Prevention
Recruiting now · Not applicable
Conditions studied: Gestational Diabetes
In brief
The goal of this randomised controlled trial is to test the effectiveness of a mobile instant messaging-based lifestyle intervention in pregnant women at risk of gestational diabetes
Key facts
- Study ID
- NCT06061991
- Run by
- The University of Hong Kong
- People needed
- 944
- Starts
- 2024-01-30
- Expected to finish
- 2026-10-30
- Last updated by the study team
- 2024-09-19
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Ethnic Chinese singleton pregnant woman in <14 weeks of gestation
- Aged 18 years or above
- Own a mobile phone with an instant messaging app
- Not participating in similar trials on diabetes or lifestyle modifications
- Have at least one of the following risk factors for GDM:
- Age ≥35 years at the expected date of delivery
- Body mass index (BMI) ≥ 25 kg/m2 pre-pregnancy or in the first trimester
- Family history of diabetes in first-degree relative
- Previous GDM or delivered a baby with birthweight ≥4 kg
You may not qualify if…
- Pre-existing diabetes or other medical conditions that may affect metabolism (e.g., thyroid disorders) or psychiatric disorders
Where it is running
- Kwong Wah Hospital — Hong Kong, Hong Kong (enrolling)
- Princess Margaret Hospital — Hong Kong, Hong Kong (enrolling)
- Queen Mary Hospital/ Tsan Yuk Hospital — Hong Kong, Hong Kong (enrolling)
- United Christian Hospital/ Tseung Kwan O Hospital — Hong Kong, Hong Kong (enrolling)
Full record on ClinicalTrials.gov
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