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The evaluation of mobile & home-based postpartum lifestyle intervention program for women with recent gestational diabetes mellitus

The evaluation of mobile & home-based postpartum lifestyle intervention program for women with recent gestational diabetes mellitus

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007497
Enrollment
108
Registered
2022-06-30
Start date
2022-02-16
Completion date
Unknown
Last updated
2022-09-20

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

Conditions

None listed

Interventions

Behavioral : - Intervention period : 6 month - Control group : Providing educational materials for healthy lifestyles. (2-time) - Intervention group : Using mobile applications for lifestyle intervent

Sponsors

The Catholic University of Korea
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: - A women with a history of gestational diabetes in recent childbirths. - Subjects who are 6-12 weeks after childbirth based on the time of participation in the study. - 19 to 45 years old - Subjects owns a smartphone based on android or IOS - Subjects who understand and voluntarily agreed to the contents of this study.

Exclusion criteria

Exclusion criteria: - Diagnosis of diabetes before pregnancy or after childbirth. - History of high-risk pregnancy (drug or alcohol abuse, pregnancy complications) - Premature birth 36 weeks before pregnancy. - Multi-fetal pregnancy with triplets or more. - Severe heart disease(NYHA grade III ~ IV), severe kidney disease(eGFR<30ml/min) - A person who has been diagnosed with a malignant tumor within the last 5 years and and receive treatment. - A person who administers systemic steroids and immunosuppressants that affect blood sugar control. - Participating in postpartum intervention studies other than this study. - Pregnancy plans during study participation period. - Communication problem.

Design outcomes

Secondary

MeasureTime frame
To compare the change of clinical levels(blood pressure, fasting blood glucose, HbA1c, lipid profiles) at pre-post intervention;To compare the change of nutritional status, physical activity status, quality of life, self-efficacy at pre-post intervention

Primary

MeasureTime frame
To compare the change of BMI at pre-post intervention

Countries

Korea, Republic of

Contacts

Public ContactSun-Young Lim

The Catholic University of Korea

sun6309@catholic.ac.kr+82-2-2258-8286

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026