ClinicalTrials.Veeva

Menu

Effects of Lifestyle Intervention on Childhood Outcomes in LGA Infants

Shanghai Jiao Tong University logo

Shanghai Jiao Tong University

Status

Enrolling

Conditions

Childhood Overweight

Treatments

Other: Comprehensive lifestyle intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT04661449
XH-20-023

Details and patient eligibility

About

Large-for-gestational-age (LGA) infants have a higher risk of metabolic disease later in life, and their postnatal growth in early childhood may be associated with long-term adverse outcomes. The purpose of this study is to explore whether comprehensive lifestyle intervention in the first year after birth in LGA infants will reduce the rate of overweight/obesity at childhood and improve neurodevelopmental outcomes and its possible mechanism.

Full description

Term LGA infants will be randomly divided into two groups shortly after birth: intervention group and control group. Infants in intervention group will attend the follow-up clinic and motor development assessment and guidance will be provided every three months in the first year. Other lifestyle interventions include feeding guidance and healthcare education. Infants in control group will routinely attend the follow-up clinic every six months. Primary outcome is the rate of overweight/obesity at two years old and seven years old. Neurodevelopmental assessment, carotid intima-media thickness (CIMT) and blood pressure at childhood will also be evaluated. The association of the outcome of LGA infants at two years old and the biomarkers in cord blood will be investigated, which includes serum leptin, insulin, insulin-like growth factors -1 (IGF-1), blood lipid series and adiponectin.

Enrollment

138 estimated patients

Sex

All

Ages

1 day to 1 month old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • term
  • large-for-gestational-age infants

Exclusion criteria

  • major genetic disorder
  • congenital anomalies
  • severe digestive disease

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

138 participants in 2 patient groups

Lifestyle Intervention
Experimental group
Description:
every 3 months within 1 year.
Treatment:
Other: Comprehensive lifestyle intervention
control group
No Intervention group
Description:
Regular follow-up every 6 months within 1 year.

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems