Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06061991

Mobile Instant Messaging-based Lifestyle Intervention for Gestational Diabetes Prevention

Led by The University of Hong Kong · Updated on 2024-09-19

944

Participants Needed

4

Research Sites

143 weeks

Total Duration

On this page

Sponsors

T

The University of Hong Kong

Lead Sponsor

R

Research Grants Council, Hong Kong

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

CONDITIONS

Official Title

Mobile Instant Messaging-based Lifestyle Intervention for Gestational Diabetes Prevention

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Ethnic Chinese singleton pregnant woman under 14 weeks of gestation
  • Aged 18 years or older
  • Owns a mobile phone with an instant messaging app
  • Not currently participating in similar diabetes or lifestyle trials
  • Has at least one risk factor for gestational diabetes: age 35 or older at delivery, pre-pregnancy or first trimester BMI of 25 or higher, family history of diabetes in a first-degree relative, previous gestational diabetes, or previous baby weighing 4 kg or more
Not Eligible

You will not qualify if you...

  • Has pre-existing diabetes
  • Has medical conditions affecting metabolism such as thyroid disorders
  • Has psychiatric disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Kwong Wah Hospital

Hong Kong, Hong Kong

Actively Recruiting

2

Princess Margaret Hospital

Hong Kong, Hong Kong

Actively Recruiting

3

Queen Mary Hospital/ Tsan Yuk Hospital

Hong Kong, Hong Kong

Actively Recruiting

4

United Christian Hospital/ Tseung Kwan O Hospital

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

T

Tzu Tsun Luk, PhD, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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