Skip to content

Effectiveness of a Mobile Health Program in Pregnant Women

Effectiveness of a Mobile Health Program on Blood Glucose and Gestational Weight Gain in Pregnant Women: A Mixed-Methods Study

Status
Enrolling by invitation
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06917703
Enrollment
160
Registered
2025-04-08
Start date
2025-04-11
Completion date
2026-10-30
Last updated
2026-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Gestational Age and Weight Conditions, Eating Behaviors, Literacy, E-learning

Keywords

pregnancy, health literacy, E-learning, gestational weight gains, nutriention

Brief 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.

Detailed description

1. Sociodemographic variables: age, education level, marital status, occupation, and socioeconomic status. 2. Obstetric variables: gravidity, history of miscarriage, pregnancy complications, and mode of delivery. 3. Pre-pregnancy BMI. 4. Dietary habits, perceived healthy eating behaviors, and dietary patterns. 5. Psychological distress and depressive symptoms. 6. Gestational blood glucose levels and GWG

Interventions

in experience group

Sponsors

Ministry of Science and Technology, Taiwan
CollaboratorOTHER_GOV
National Taipei University of Nursing and Health Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Intervention model description

To assess the effectiveness of the i-PregMom mobile application and digital dietary image recording on blood glucose control and gestational weight gain, a randomized controlled design with a double repeated measures approach will be conducted (Intervention group: n=80; Control group: n=80). Data will be collected at three time points: * Baseline (10-14 weeks of gestation) * Two weeks post-intervention (12-16 weeks of gestation) * Three months post-intervention (24-28 weeks of gestation) The intervention group will receive face-to-face nutrition education (15-30 min/session) based on the Health Promotion Administration's pregnancy dietary guidelines and access to the i-PregMom mobile application for continuous dietary management. The control group will receive only face-to-face nutrition education (15-30 min/session) based on standard pregnancy dietary guidelines.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

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).

Design outcomes

Primary

MeasureTime frameDescription
Gestational Weight Gain in Pregnanto 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.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.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026