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Postpartum Weight Loss and Sleep Amongst Obese Women

NCT01968330 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2016-05-20

No results posted yet for this study

Summary

This study will be a randomized controlled trial involving obese women obtaining prenatal care at an obstetric care clinic. Study subjects will undergo prenatal care in a group setting or prenatal care with a behavioral intervention to improve sleep. Anthropometric measurements, blood draws, questionnaires and at home sleep studies will be completed at three specified times (two antepartum and one postpartum). Primary outcome will be a comparison of postpartum weight loss amongst the intervention and control groups.

Conditions

Interventions

BEHAVIORAL

Go!®to sleep

Sponsors & Collaborators

  • University of South Florida

    lead OTHER

Principal Investigators

  • Mary A Cain, MD · University of South Florida Department of OBGYN

  • Judette Louis, MD, MPH · University of South Florida Department of Obstetrics and Gynecology

  • Linda Odibo · University of South Florida Department of Obstetrics and Gynecology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-05-31
Primary Completion
2016-05-31
Completion
2016-05-31

Countries

  • United States

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 NCT01968330 on ClinicalTrials.gov