A Study of the Intervention of Time-restricted Eating in High-risk Populations of GDM

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-50
SponsorFudan University

About this trial

This is a randomized controlled trial, aiming to investigate whether a time-restricted eating (TRE) can reduce the incidence of gestational diabetes mellitus (GDM) in high-risk pregnant women. Investigators intend to conduct a 3-month randomized controlled study to compare the effects of 10-hour TRE and habitual eating time on GDM .

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 18-50 years;

The risk for GDM includes overweight or obesity (BMI ≥ 24 kg/m2 before pregnancy), first-degree relative with diabetes, history of cardiovascular disease, hypertension (≥130/80 mmHg or on therapy for hypertension), HDL cholesterol level < 1 mmol/L and/or a triglyceride level > 2.8 mmol/L, history of GDM, history of macrosomia delivery, individuals with polycystic ovary syndrome, repeated positive fasting urine glucose in the first trimester, or age>45 years according to Guideline of Diagnosis and Treatment of Hyperglycemia in Pregnancy (2022);

Less than 14 weeks of gestation;

Able to read and complete questionnaires in Chinese;

Disqualifiers

Pregestational diabetes (including diabetes diagnosed before conception; fasting blood glucose ≥ 7.0 mmol/L or HbA1c ≥ 6.5% in the first trimester; typical symptoms of hyperglycemia or hyperglycemic crisis with optional blood glucose ≥ 11.1 mmol/L);

Impaired glucose tolerance (including fasting blood glucose ≥ 5.6 mmol/L or two fasting blood glucose ≥ 5.1 mmol/L in the first trimester);

Current or recent use of drugs that affect glucose metabolism such as metformin, glucocorticoids and Orlistat;

Severe comorbidities (including cardiac diseases, kidney diseases, hepatopathy, autoimmune diseases, uncontrolled thyroid disease, previous or current malignant tumors, etc.);

Trial design

Design model

Parallel

Treatments tested in this trial

  • Time-limited eating

    Behavioral

    All participants will be instructed to follow a diet of 1800-2200 kcal/d (45-50% of energy from carbohydrate, 15-20% from protein, 25-30% from fat) based primarily on Dietary Guidelines for Chinese Residents (2022), Dietary guidelines for pregnant women and Guideline of Diagnosis and Treatment of Hyperglycemia in Pregnancy (2022). Participants assigned to the TRE group will be instructed to consume prescribed calories in a 10-hour eating window (from 8:30 am to 18:30 pm) each day and only noncaloric beverages were permitted outside of the eating window over 3 months (from 14-26 gestational weeks). Participants in the SOC group will be instructed to consume prescribed calories following habitual daily eating schedule over 3 months.

Treatment groups

240 Participants
are divided into 2 treatment groups
Group A: TRE(Time-restricted eating group)Experimental treatment 1 intervention
Group B: SOC (standard of care group)No intervention 0 interventions

Trial outcomes

Primary outcomes

1

The incidence of GDM

Diagnosed by the 75g oral glucose tolerance test (OGTT).

Time frame
26 gestational weeks

Secondary outcomes

1

Number of newborns with macrosomia

Number of newborns with birth weight ≥4000g.

Time frame
At delivery
2

Number of newborns with low birth weight

Number of newborns with birth weight \<2500g.

Time frame
At delivery
3

Number of newborns large for gestational age (LGA)

Number of newborns with weight lies above the 90th percentile for the gestational age.

Time frame
At delivery
4

Number of newborns small for gestational age (SGA)

Number of newborns with weight lies below the 10th percentile for the gestational age.

Time frame
At delivery

Other outcomes

1

Adherence to the intervention

Adherence to the intervention measure by Chinese Dietary Guidelines Compliance Index for Pregnant Women (CDGCI-PW) and by counting the number of days in which participants consumed calories outside the time-window or exceeding the upper limit of the required energy intake. Chinese Dietary Guidelines Compliance Index for Pregnant Women (CDGCI-PW): Scores range from 0-100, with higher score indicating better adherence.

Time frame
From 14-26 gestational weeks

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Fudan University

Lead sponsor

Obstetrics & Gynecology Hospital of Fudan University

Sponsor institution

Shenzhen Maternity & Child Healthcare Hospital

Collaborator