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Recruiting NCT06061991

NCT06061991 Mobile Instant Messaging-based Lifestyle Intervention for Gestational Diabetes Prevention

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Clinical Trial Summary
NCT ID NCT06061991
Status Recruiting
Phase
Sponsor The University of Hong Kong
Condition Gestational Diabetes
Study Type INTERVENTIONAL
Enrollment 944 participants
Start Date 2024-01-30
Primary Completion 2026-07-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Mobile instant messaging-based lifestyle interventionText messaging remindersBrief advice on GDM prevention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 944 participants in total. It began in 2024-01-30 with a primary completion date of 2026-07-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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

Eligibility Criteria

Inclusion Criteria: 1. Ethnic Chinese singleton pregnant woman in \<14 weeks of gestation 2. Aged 18 years or above 3. Own a mobile phone with an instant messaging app 4. Not participating in similar trials on diabetes or lifestyle modifications 5. 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 Exclusion Criteria: * Pre-existing diabetes or other medical conditions that may affect metabolism (e.g., thyroid disorders) or psychiatric disorders

Contact & Investigator

Central Contact

Tzu Tsun Luk, PhD, RN

✉ luktt@connect.hku.hk

📞 +852-3917-7574

Principal Investigator

Tzu Tsun Luk, PhD, RN

PRINCIPAL INVESTIGATOR

The University of Hong Kong

Frequently Asked Questions

Who can join the NCT06061991 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Gestational Diabetes. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06061991 currently recruiting?

Yes, NCT06061991 is actively recruiting participants. Contact the research team at luktt@connect.hku.hk for enrollment information.

Where is the NCT06061991 trial being conducted?

This trial is being conducted at Hong Kong, Hong Kong, Hong Kong, Hong Kong, Hong Kong, Hong Kong, Hong Kong, Hong Kong.

Who is sponsoring the NCT06061991 clinical trial?

NCT06061991 is sponsored by The University of Hong Kong. The principal investigator is Tzu Tsun Luk, PhD, RN at The University of Hong Kong. The trial plans to enroll 944 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology