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The LATCHING Pilot Project

Learning About Techniques to Create Healthy Infants Through Nutrition and Proper Growth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03442517
Enrollment
46
Registered
2018-02-22
Start date
2017-04-29
Completion date
2019-05-05
Last updated
2019-05-30

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

Conditions

Breastfeeding

Keywords

group-based counseling, phone counseling, conference calls

Brief summary

The purpose of this study is to learn if group-based phone counseling is effective for increasing breastfeeding rates, reducing the early introduction of solids and increasing maternal weight loss after pregnancy.

Interventions

BEHAVIORALBehavior Lifestyle Intervention

Participants will be involved in group-based counseling. Sessions will be about 1 hour each and comprise up to 10 people. The sessions will be led by a trained health educator. The calls will be a chance for participants to discuss challenges with breastfeeding, problem solving skills, educational information, and discuss balanced diet topics.

Participants will receive the standard education given by their OBGYN or other healthcare provider. No additional breastfeeding, nutrition or postpartum weight loss education will be provided to participants by the investigators during pregnancy. After delivery, participants will follow normal pediatric visit schedule.

Sponsors

University of Kansas Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Women who are 9-30 weeks in gestation that have not previously met breastfeeding recommendations * Speak and understand English

Exclusion criteria

* Women with pregnancies conceived using fertility treatments, those at high risk for pre-term delivery, those with multiple gestation (ie. twins, triplets, etc), or pregnancies complicated by morbid obesity (BMI\>40), diabetes (pre-gestational or gestational), hypertension, metabolic dysfunction, etc. * Women who have previously exclusively breastfed an infant for three or more months

Design outcomes

Primary

MeasureTime frame
Proportion of women who introduce solidsMonth 4
Differences in infant feeding progressionMonth 6
Proportion of women exclusively breastfeedingMonth 6

Secondary

MeasureTime frameDescription
Study RetentionMonth 6Retention rates will be calculated from participants who complete feeding questionnaire data at 6 months.
Subject satisfaction and acceptability of interventionWeek 24Structured interviews will be used to determine subject satisfaction. Structured interviews will obtain descriptive data regarding problems encountered by participants during the intervention, areas of intervention strength and weakness, information participants found helpful and information participants wish they had been given during the intervention, and ways the overall intervention could be improved.
Intervention complianceWeek 24Compliance rates will be calculated from participants that attend at least 66.6% (at least 4 sessions) of GBPC sessions.

Other

MeasureTime frame
Differences in infant feeding progressionWeek 2

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 22, 2026