The summary of diabetes self-care activities measure: results from 7 studies and a revised scale.
D J Toobert, S E Hampson, R E Glasgow
https://pubmed.ncbi.nlm.nih.gov/10895844Actively Recruiting
Led by Hong Kong Metropolitan University · Updated on 2026-05-22
30
Participants Needed
1
Research Sites
N/A
Total Duration
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
Feasibility Testing of the "MyGlucoCare" Smartphone App for Women With Gestational Diabetes
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
Total: 1 location
1
Hong Kong Metropolitan University
Hong Kong, Hong Kong
Actively Recruiting
B
Bronya Luk Assistant Professor, DHSc, MN, BN
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
D J Toobert, S E Hampson, R E Glasgow
https://pubmed.ncbi.nlm.nih.gov/10895844Philip L Ritter, Kate Lorig, Diana D Laurent
https://pubmed.ncbi.nlm.nih.gov/26846336Ben O'Neill
https://pubmed.ncbi.nlm.nih.gov/35167592K Kroenke, R L Spitzer, J B Williams
https://pubmed.ncbi.nlm.nih.gov/11556941