Dietary Management of Gestational Diabetes Mellitus

Not Applicable

Not yet recruiting

• Conditions: Gestational Diabetes Mellitus in Pregnancy; Diet; Healthy
• Interventions: Behavioral: diet management program based on the nudge strategy

• Registration Number: NCT05613920
• Lead Sponsor: Qingdao University

Brief Summary

The goal of this clinical trial is to test effect of dietary management program based on the nudge strategy in gestational diabetes mellitus patients. The main questions it aims to answer is whether the dietary management program is effective for the diet management behavior of gestational diabetes mellitus patients.

Participants will receive a 12 week dietary management program. The intervention group will receive a diet management program based on the nudge strategy, and the control group will receive a routine dietary management program. Researchers will compare two group's glycemic control and pregnancy outcomes and to see if effective for the diet management behavior.

Detailed Description

Not available

Study Timeline

• Status Verified: 2022-10
• Study First Submitted: 2022-10-21
• Study First Submitted QC: 2022-11-08
• Last Update Submitted: 2022-11-08
• Study Start: 2022-11-10
• Study First Posted: 2022-11-14
• Last Update Posted: 2022-11-14
• Primary Completion: 2022-12
• Study Completion: 2023-02

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: Female
• Target Recruitment: 48

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
diet management program based on the nudge strategy	diet management program based on the nudge strategy	The intervention group will receive a diet management program based on the nudge strategy

Primary Outcome Measures

Name	Time	Method
Changes in blood glucose levels over time	Pre-intervention, 1-month post-intervention and 3-months post-intervention	With the change of intervention and time, it is better for the fasting blood glucose to decrease; With the change of intervention and time, it is better that the 1hPG decreases; With the change of intervention and time, it is better that the 2hPG decreases.

Secondary Outcome Measures

Name	Time	Method
pregnancy outcomes	During the delivery of pregnant women, the relevant data of pregnancy outcome were collected by consulting medical records or telephone follow-up.	Number of Participants with Premature, Cesarean delivery, Gestational hypertension, Giant baby, Fetal intrauterine distress

Trial Locations

Locations (1)

Wenyao Geng; 🇨🇳 Qingdao, Shandong, China