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eMOMS of Rochester

NCT01331564 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1641

Last updated 2015-12-02

No results posted yet for this study

Summary

The project aims to develop, implement and evaluate electronically-mediated behavioral intervention programs for pregnant and postpartum women in order to prevent excessive weight gain during pregnancy and postpartum weight retention.

Conditions

  • Gestational Weight Gain
  • Postpartum Weight Retention

Interventions

BEHAVIORAL

electronic intervention during pregnancy and postpartum

Electronically-mediated behavioral interventions to encourage women to gain an appropriate amount of weight during pregnancy and to follow a healthy lifestyle postpartum to minimize postpartum weight retention

BEHAVIORAL

electronic intervention during pregnancy

Electronically-mediated behavioral interventions to encourage women to gain an appropriate amount of weight during pregnancy.

BEHAVIORAL

Control

Control women will receive non-weight related content during both time periods at the project website.

Sponsors & Collaborators

Principal Investigators

  • Isabel D Fernandez, MD, MPH, PhD · University of Rochester

  • Christine M Olson, PhD · Cornell University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2014-05-31
Completion
2014-12-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT01331564 on ClinicalTrials.gov