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Clinical Trial Summary

The study will test the effectiveness of a smartphone-based behavior modification program adapted for use in Women, Infants, and Children program in a state-wide, randomized controlled trial in 432 low-income women enrolled in the Louisiana Women, Infants, and Children program.


Clinical Trial Description

The study is a multi-site randomized controlled trial, testing the effectiveness of the smartphone-based behavior modification program in pregnant women within the Louisiana Women, Infants, and Children program. Equal number of participants will be randomized to either the intervention or the control. Although the intervention itself lasts 24 weeks (only during pregnancy), women will be enrolled in this study for approximately 18 months, from the 10-16th week of pregnancy until 12 month postpartum follow-up. Study outcomes will be assessed at three visits during pregnancy (early, mid, and late,) and three visits postpartum (1, 6, and 12 months). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04028843
Study type Interventional
Source Pennington Biomedical Research Center
Contact
Status Active, not recruiting
Phase N/A
Start date July 12, 2019
Completion date August 31, 2025

See also
  Status Clinical Trial Phase
Completed NCT01858233 - The IBEP Study: an Intervention for Lifestyle Modification in Women With Gestational Diabetes N/A
Completed NCT01610752 - Personalized Management of Body Weight During Pregnancy N/A