A Personalized Telehealth Intervention for Health and Weight Loss in Postpartum Women
- Conditions
- Postpartum Weight Retention
- Interventions
- Behavioral: WIC E-Moms
- Registration Number
- NCT01751230
- Lead Sponsor
- Pennington Biomedical Research Center
- Brief 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.
- Detailed Description
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:
1. WIC Moms: receive advice and services for nutrition and weight management after pregnancy from their WIC clinic.
2. 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 40
- 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
- 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)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description WIC E-Moms WIC E-Moms If picked for this group, you will receive a personalized diet and exercise plan to help you lose the weight you gained during your pregnancy. All information will be given to you using a SmartPhone, such as an iPhone. You can use your own phone or one can be loaned to you for the study. You will also be loaned a scale so you can weigh yourself at home. You will also get advice and services from your WIC clinic.
- Primary Outcome Measures
Name Time Method Body Weight Change Baseline and 16 weeks The primary outcome measure is weight change after the 16 week intervention.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Pennington Biomedical Research Center
🇺🇸Baton Rouge, Louisiana, United States