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Completed

NCT Number: NCT01751230

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 the app.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Pennington Biomedical Research Center

Baton Rouge, Louisiana, 70808, United States

About this study

The E-Moms Study will last about 4 months. The weight management program is 4 months long and will end about 6 months after the participant's baby is born. All participants will receive Women, Infants and Children (WIC) services.

For the weight management program, participants will be put into one of these groups:

  • WIC Moms: receive advice and services for nutrition and weight management after pregnancy from their WIC clinic.
  • WIC E-Moms: receive a personalized diet and exercise plan to help them lose the weight they gained during their pregnancy. All information will be given to them using a SmartPhone, such as an iPhone. They will also get advice and services from your WIC clinic.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Are a female who has delivered a baby within the last 2 months
  • Are 18 years of age or older
  • Have a body mass index ≥25 kg/m2 or <40 kg/m2
  • Are accepted for post-pregnancy WIC services
  • Are English-speaking

Exclusion criteria

  • Are participating in the Nurse Family Partnership program
  • Had multiples in your most recent pregnancy
  • Are unwilling to be assigned at random to either of the 2 study groups
  • Are planning to move out of the study area within the next 6 months
  • Have a history of psychiatric conditions or chronic disease than can impact body weight, appetite, or energy intake such as HIV/AIDS, cancer, bipolar disorder or schizophrenia
  • Currently use antipsychotic medications or have used such medications in the previous 12 months
  • Have been diagnosis with type I diabetes
  • Report having a heart attack, stroke, or being hospitalized or treated for chest pain
  • Currently taking medications or supplements to aid in weight loss
  • Have had weight loss surgery in the past year or plan to have it prior to study completion.
  • Currently participating in another interventional study that influences weight control
  • Currently abusing drugs or alcohol (up to 14 drinks per week allowed)

Treatment and study plan

WIC E-Moms

Behavioral

Participants enrolled in the E-Moms group will receive a personalized dietary prescription to promote weight loss and arrive at pregravid weight by 6 months postpartum. Our weight loss intervention will incorporate standard WIC nutritional advice and will encouraged 150 minutes/week of moderate intensity activity, which is about 3,000 - 4,000 steps/day above baseline, as recommended for maintenance of healthy weight. Each participant will be assigned a trained weight management counselor who will provide frequent recommendations and advice and support at least once per week.

Other names: E-Moms

Primary outcomes

  1. Body Weight Change

    Time frame: Baseline and 16 weeks

    The primary outcome measure is weight change after the 16 week intervention.

Sponsors and collaborators

Lead sponsor

Pennington Biomedical Research Center

Other

Collaborators

  • United States Department of Agriculture (USDA)
  • University of California, Los Angeles

Registry information

Official study title

E-Moms: A Personalized Telehealth Intervention for Health and Weight Loss in Postpartum Women

Acronym: E-Moms

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Dec 17, 2012
Registry last updated
Aug 24, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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