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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: Completed NA study of Postpartum Weight Retention, sponsored by Pennington Biomedical Research Center.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
The primary outcome measure is weight change after the 16 week intervention.
Conditions Studied
Interventions
- BEHAVIORAL WIC E-Moms
Study Locations (1)
Louisiana
- Pennington Biomedical Research Center - Baton Rouge
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2013-08 |
| Est. Completion | 2014-10 |
| Phase | NA |
What the finished NCT01751230 record still lists
NCT01751230 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 332-participant average among 7 other Postpartum Weight Retention trials with a reported enrollment target (88% lower).
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 a single indexed study location in 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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