NCT06372860Completed
DPP Feasibility Study of Breastfeeding - eMOMS 2.0
Diabetes Prevention Program Feasibility Study of Breastfeeding - Electronic Monitoring of Mom's Schedule 2.0
Source: ClinicalTrials.gov · Last updated 18 Dec 2025
Brief summary (registry, in English)
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.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 43 (actual)
- First submitted
- 4 Apr 2024
- Start date
- 30 Apr 2024
- Primary completion date
- 31 Aug 2025
- Lead sponsor
- University of Kansas Medical Center
- Diseases
- Obesity
- NCT number
- NCT06372860
What you commit to
- Study type: Interventional
- Participants enrolled: 43
- From 30 Apr 2024 to the primary completion date, 31 Aug 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior bariatric surgery
Other illness
- Thyroid disease
- Presence of any condition that limits walking
- Presence of any condition that limits following diet recommendations
- Pregnancies complicated with fetuses diagnosed with lethal malformations/conditions
Other
- Complications related to pregnancy that require emergency care
- Multiple gestation
- Substance abuse within last 3 years
- Assisted reproductive technology (ART)-related pregnancy
- Current smoker
- In weight-loss program within 3 months of conception
- BMI \>/= 35
- Unable to attend intervention/ follow-up visits
- Unwilling to self-monitor data collection
- Unable to complete intervention
Who the study is looking for
- Pregnant
- In second trimester or early third trimester
- BMI \>/= 25 and \< 35
- At least 18 years old or older
- Able to read and understand English
- Able to learn and use a video platform
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Via Christi Maternal Fetal Medicine Clinic Coordinator of this site? Confirm its status | Wichita | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.