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Using Digital Health Technologies to Prevent Rapid Infant Weight Gain.

Using Digital Health Technologies to Prevent Rapid Infant Weight Gain.

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05265845
Enrollment
0
Registered
2022-03-04
Start date
2024-02-29
Completion date
2024-07-31
Last updated
2024-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bottle Feeding, Breastfeeding, Child Obesity

Brief summary

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.

Interventions

BEHAVIORALIntervention

The intervention aims to support infant feeding decisions and teach responsive feeding strategies.

BEHAVIORALText4Baby

Free health and wellness text messages timed to due date through pregnancy and up until the baby's first birthday.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
Engagement32 weeks gestation to 3 months postpartumPercent of text messages responded to as measured by text log.

Secondary

MeasureTime frameDescription
Breastfeeding duration0 to 3 months postpartumNumber of weeks breastfed as measured by patient response.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026