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NCT01751230 · ClinicalTrials.gov registry record · NA

A Personalized Telehealth Intervention for Health and Weight Loss in Postpartum Women

A NA study of Postpartum Weight Retention, sponsored by Pennington Biomedical Research Center.

Completed
Registry status
NA
Development phase
40
Enrollment target
1
Study location

NCT01751230 is a NA study of Postpartum Weight Retention that has completed, run by Pennington Biomedical Research Center. The registered enrollment target is 40 participants, below the 332-participant average among 7 other Postpartum Weight Retention trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01751230, a NA study of Postpartum Weight Retention, has completed, sponsored by Pennington Biomedical Research Center.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to help women lose the weight they gained during their pregnancy using a SmartPhone app the investigators have developed called E-Moms. The investigators hypothesize that the moms given the app to use during the study will lose more weight than the moms who do not use the app.

Interventions

  • BEHAVIORAL WIC E-Moms

Study Locations (1)

Louisiana

  • Pennington Biomedical Research Center - Baton Rouge

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2013-08
Est. Completion 2014-10
Phase NA

What the Registry Record Tells You About NCT01751230

The ClinicalTrials.gov registry entry for NCT01751230 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 332-participant average among 7 other Postpartum Weight Retention trials with a reported enrollment target (88% lower). The listed sponsor is Pennington Biomedical Research Center, which has 258 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Postpartum Weight Retention appearing as the primary indexed condition, and to 1 intervention - of which WIC E-Moms is the first listed.

NCT01751230 reports 1 study location spanning 1 distinct geographic area - top geographies include Louisiana.

Frequently Asked Questions

What is clinical trial NCT01751230 about?

NCT01751230 is a clinical study titled "A Personalized Telehealth Intervention for Health and Weight Loss in Postpartum Women". The purpose of this study is to help women lose the weight they gained during their pregnancy using a SmartPhone app the investigators have developed called E-Moms. The investigators hypothesize that the moms given the app to use during the study will lose more weight than the moms who do not use th...

What is the current status of trial NCT01751230?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2013-08. Estimated completion is 2014-10.

What conditions does trial NCT01751230 study?

This clinical trial studies the following conditions: Postpartum Weight Retention.

What interventions are being tested in trial NCT01751230?

The interventions under investigation include: WIC E-Moms (BEHAVIORAL).

Who is sponsoring clinical trial NCT01751230?

This trial is sponsored by Pennington Biomedical Research Center, which has 258 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01751230 being conducted?

This trial has 1 study location across Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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