Effectiveness of a Mobile Health Program in Pregnant Women (NCT06917703) | Clinical Trial Compass
By InvitationNot Applicable
Effectiveness of a Mobile Health Program in Pregnant Women
Taiwan160 participantsStarted 2025-04-11
Plain-language summary
1. To evaluate the usability and user experience of the i-PregMom mobile application and digital dietary image recording among pregnant women.
2. To examine the effectiveness of digital mobile health interventions on blood glucose levels and gestational weight gain among pregnant women from 10-14 weeks to 24-28 weeks of gestation.
Who can participate
Age range
18 Years – 50 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Primiparous women aged ≥18 years.
Singleton pregnancy.
Pregnant women between 10 and 14 weeks of gestation, with gestational age calculated based on the first day of the last menstrual period.
Able to listen, speak, read, and write in Chinese.
Willing to provide prenatal weight and blood glucose data.
Possess a mobile communication device (such as a smartphone or social media account) and be able to receive emails.
Exclusion Criteria:
* Engaged in weight loss activities prior to pregnancy.
Diagnosed with chronic illnesses that may affect weight changes (e.g., psychiatric disorders, thyroid diseases).
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Gestational Weight Gain in Pregnant
Timeframe: o Gestational Weight Gain (GWG) will be recorded three times (10-14, 12-16, and 24-28 weeks of gestation) based on maternity health records to analyze trends in weight changes and the impact of the mobile health intervention.
Trial details
NCT IDNCT06917703
SponsorNational Taipei University of Nursing and Health Sciences