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Using Digital Health Technologies to Prevent Rapid Infant Weight Gain.

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Duke University

Status

Withdrawn

Conditions

Breastfeeding
Child Obesity
Bottle Feeding

Treatments

Behavioral: Intervention
Behavioral: Text4Baby

Study type

Interventional

Funder types

Other

Identifiers

NCT05265845
Pro00109854

Details and patient eligibility

About

A digital intervention to provide supplemental infant feeding support to mothers enrolled in WIC. The trial begins prenatally and continues through 3-months postpartum and tests the feasibility and acceptability of a text messaging intervention aimed at increasing responsive bottle feeding as well as breastfeeding duration and exclusivity among mothers enrolled in WIC using evidence-based components such as interactive self-monitoring and feedback.

Recruitment and enrollment never started at Duke for the Intervention represented in this record. The overall status of recruiting and actual start date were previously entered in error.

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Enrolled in WIC, English or Spanish speaking, at least 18 years old, between 18-28 weeks' gestation, and planning to remain enrolled in WIC for 6 months, intention to breastfeed or undecided about breastfeeding, and willingness to send and receive daily text messages.

Exclusion criteria

  • Postpartum exclusions include infant prematurity (<37 weeks), >3 days in neonatal intensive care unit, major medical problem affecting breastfeeding (i.e., maternal HIV), or birth weight <5 lbs.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Triple Blind

0 participants in 2 patient groups

Intervention
Experimental group
Description:
Interactive text messages that include goal setting, tailored feedback, and skills training.
Treatment:
Behavioral: Intervention
Control
Active Comparator group
Description:
Text4Baby
Treatment:
Behavioral: Text4Baby

Trial contacts and locations

1

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Central trial contact

Javier Rodriguez, AS; Melissa C Kay, PhD

Data sourced from clinicaltrials.gov

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