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

Not Applicable

Recruiting

• Conditions: Not Applicable

• Registration Number: KCT0007497
• Lead Sponsor: The Catholic University of Korea

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 20 September 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 108

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

- 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.

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the change of BMI at pre-post intervention

Secondary Outcome Measures

Name	Time	Method
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