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Electronic-personalized Program for Obesity in Pregnancy to Improve Delivery

NCT02924636 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 857

Last updated 2025-12-11

No results posted yet for this study

Summary

The purpose of this study is to assess the efficacy of an electronic-based intervention to help pregnant overweight and obese women gain an appropriate amount of weight and improve their delivery i.e. to reduce the rate of labour procedures and interventions. We chose a composite outcome including instrumental delivery and Caesarean section, as clinically relevant outcomes because the mode of delivery is one of the major goals of the obstetrical management and is is strongly associated with body mass index and gestational weight gain.

Conditions

Interventions

BEHAVIORAL

ePPOP-ID program

This is a personalized and online program. The website will provide secure communication with dietician and lifestyle coaches.

Sponsors & Collaborators

  • Ministry of Health, France

    collaborator OTHER_GOV

  • University Hospital, Lille

    lead OTHER

Principal Investigators

  • Philippe Deruelle, MD, PhD · University Hospital, Lille

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-13
Primary Completion
2022-03-13
Completion
2022-04-13

Countries

  • France

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02924636 on ClinicalTrials.gov