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NCT06372860 · ClinicalTrials.gov registry record · NA

DPP Feasibility Study of Breastfeeding - eMOMS 2.0

A NA study, sponsored by University of Kansas Medical Center.

Completed
Registry status
NA
Development phase
43
Enrollment target

NCT06372860 is a NA study that has completed, run by University of Kansas Medical Center. The registered enrollment target is 43 participants.

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The verdict

NCT06372860, a NA study, has completed, sponsored by University of Kansas Medical Center.

COMPLETED
Registry status
NA
Development phase
43 participants
Enrollment target

Study Summary

The purpose of this study is to investigate the impact of a comprehensive intervention that combines breastfeeding support with a diabetes prevention-based program (DPP) on postpartum weight retention and lactation duration among women with pre-pregnancy overweight or obesity. This intervention, named eMOMS, is delivered by a certified health coach via a mobile health (mHealth) application.

Interventions

  • BEHAVIORAL Usual Care
  • BEHAVIORAL Breastfeeding
  • BEHAVIORAL Diabetes Prevention Program

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2024-04-30
Est. Completion 2025-08-31
Phase NA

Sponsor

University of Kansas Medical Center

408 total trials

What the Registry Record Tells You About NCT06372860

The ClinicalTrials.gov registry entry for NCT06372860 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Kansas Medical Center, which has 408 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Usual Care is the first listed.

NCT06372860 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06372860 about?

NCT06372860 is a clinical study titled "DPP Feasibility Study of Breastfeeding - eMOMS 2.0". The purpose of this study is to investigate the impact of a comprehensive intervention that combines breastfeeding support with a diabetes prevention-based program (DPP) on postpartum weight retention and lactation duration among women with pre-pregnancy overweight or obesity. This intervention, nam...

What is the current status of trial NCT06372860?

This trial is currently completed. It is a NA study. The enrollment target is 43 participants. The study started on 2024-04-30. Estimated completion is 2025-08-31.

What interventions are being tested in trial NCT06372860?

The interventions under investigation include: Usual Care (BEHAVIORAL), Breastfeeding (BEHAVIORAL), Diabetes Prevention Program (BEHAVIORAL).

Who is sponsoring clinical trial NCT06372860?

This trial is sponsored by University of Kansas Medical Center, which has 408 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.