Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID07372872

Development and Feasibility Testing of the MyGlucoCare Smartphone-Based Self-Management Support Program for Women With Gestational Diabetes

Led by Hong Kong Metropolitan University · Updated on 2026-05-22

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate the "MyGlucoCare" smartphone program designed to support women with gestational diabetes mellitus (GDM). The study's main goal is to test if this program is practical and acceptable for participants, and to observe preliminary effects on diabetes self-management, blood sugar control, and overall well-being. It is a single-arm pilot study involving about 30 pregnant women with GDM. Participants will use the "MyGlucoCare" app for 8 to 12 weeks during pregnancy. The program includes three components: automated personalized education covering GDM management topics, proactive individualized support from a clinician through bi-weekly check-ins and chat responses, and a moderated peer support group to share experiences. Data will be collected before starting, near the end of pregnancy, and postpartum. Women taking part will complete questionnaires, record health data, and some may participate in interviews to share feedback. Researchers will measure engagement with the app, recruitment and retention rates, system usability, self-efficacy, blood glucose levels, physical activity, stress, and pregnancy outcomes. Safety and confidentiality will be maintained throughout, with data collected securely and anonymously.

CONDITIONS

Brief Title

Feasibility Testing of the "MyGlucoCare" Smartphone App for Women With Gestational Diabetes

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women diagnosed with Gestational Diabetes Mellitus (GDM) via a 75g Oral Glucose Tolerance Test conducted between 24 and 28 weeks of gestation
  • Aged 18 years or older
  • Own a smartphone with reliable internet access
  • Able to read and understand Chinese
Not Eligible

You will not qualify if you...

  • Pre-existing diagnosis of Type 1 or Type 2 diabetes mellitus
  • Known major fetal anomaly
  • Concurrent enrollment in any other structured GDM self-management intervention
  • Severe mental health conditions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - 8 to 12 weeks

Participants use the MyGlucoCare smartphone app, which provides personalised education, clinician support, and peer support to help manage gestational diabetes.

Bi-weekly clinician check-ins and ongoing app engagement

Follow-up

Duration - Up to approximately 16 weeks after implementation

Participants complete post-intervention assessments around 36 weeks' gestation and postpartum evaluations 6-12 weeks after delivery to measure outcomes and experiences.

3 data collection points: post-intervention and postpartum assessments conducted remotely

Trial Site Locations

Total: 1 location

1

Hong Kong Metropolitan University

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

B

Bronya Luk Assistant Professor, DHSc, MN, BN

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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