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Clinical Trials/NCT04028843
NCT04028843CompletedNot Applicable

SmartMoms in WIC: A Smartphone Intervention for WIC Mothers to Improve Nutrition and Weight Gain During Pregnancy

Pennington Biomedical Research Center2 sites in 1 country351 target enrollmentStarted: July 12, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
351
Locations
2
Primary Endpoint
Number of Women Who Have Appropriate Gestational Weight Gain

Study Overview

Brief 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.

Detailed 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

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Less than 16 weeks gestational age at screening visit
  • •Have a BMI of 18.5 to 40 kg/m2
  • •Expecting a singleton pregnancy
  • •Certified to receive Women, Infants, and Children services during current pregnancy
  • •Has smartphone with internet access
  • •Willing to be identifiable to other study participants in this study program

Exclusion Criteria

  • •Drug or alcohol use
  • •Non-pregnancy related illness
  • •Hypertension at screening visit
  • •Current mental health issue or eating disorder
  • •Inability to complete a behavioral run-in task
  • •Plans to move out of the state in the next 18 months

Arms & Interventions

WIC Nutrition

No Intervention

Participants will receive weight management advice and care through the standard Women, Infants, and Children program. They will also receive weekly health information related to pregnancy, birth, and infant health through a closed Facebook group.

Healthy Beginnings

Experimental

Participants will receive the SmartMoms smartphone application, a wireless connected scale, and a Fitbit. The Healthy Beginnings program includes a 24 week intensive behavior modification program that targets healthy gestational weight gain through self-monitoring of weight and activity data, automated prescriptive feedback from the SmartMoms smartphone application, personalized feedback from counselors, and evidence-based behavioral intervention delivered throughout pregnancy.

Intervention: Healthy Beginnings (Behavioral)

Outcomes

Primary Outcomes

Number of Women Who Have Appropriate Gestational Weight Gain

Time Frame: Approximately 6 months (from 10-16 weeks gestation to 35-38 weeks gestation)

Number of pregnant women who gain appropriate weight during pregnancy as recommended by the Institute of Medicine Gestational Weight Gain guidelines

Secondary Outcomes

  • Gestational Weight Gain Per Week(Approximately 6 months (from 10-16 weeks gestation to 35-38 weeks gestation))
  • Total Gestational Weight Gain(Approximately 6 months (from 10-16 weeks gestation to 35-38 weeks gestation))
  • Gestational Weight Gain Per Week(Approximately 6 months (from 10-16 weeks gestation to 35-38 weeks gestation))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Leanne Redman

Professor

Pennington Biomedical Research Center

Study Sites (2)

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