Increase Breastfeeding Duration Among Puerto Rican Mothers

Not Applicable

Completed

• Conditions: Breastfeeding
• Interventions: Behavioral: Contingency Management

• Registration Number: NCT02148237
• Lead Sponsor: Treatment Research Institute

Brief Summary

This study is to determine preliminary effects of home-based individual breastfeeding consultation with and without cash incentives to increase breastfeeding (BF) duration among low-income Puerto Rican mothers enrolled in a Special Supplemental Nutrition Program for Women, Infants, and Children (WIC).

Detailed Description

This study is to determine feasibility, acceptability, and preliminary effect sizes of home-based individual breastfeeding consultation alone and combined with financial incentives to increase breastfeeding (BF) duration among low-income Puerto Rican mothers. These interventions will be tested in a Women, Infants, and Children (WIC) program, which capitalizes on the current goals of WIC and on the current practice of using incentives to support BF - factors that are likely to increase potential for sustainability and dissemination of the intervention. We will follow a three phase strategy. During the Formative Phase we will consult WIC staff, Puerto Rican postpartum mothers, and experts in BF, behavioral health incentives, and WIC populations and settings to develop intervention and research manuals. During the Implementation Phase, we will pilot the interventions and research procedures. We will randomly assign 60 Puerto Rican women who initiate BF to: Treatment-as-Usual (TAU) or TAU with financial incentives (also known as Contingency Management; (CM). A bilingual breastfeeding counselor visits participants at home for problem solving issues around breastfeeding. Participants also receiving CM will receive cash incentives if they show breastfeeding. We will conduct assessments at baseline, 1, 3, and 6 months postpartum, measuring BF duration, BF exclusivity, BF self-efficacy, and infant weight gain. In the Evaluative Phase, we will examine monthly recruitment, consent, and enrollment rates, as well as attendance and retention rates for the interventions and for research participation (i.e., feasibility and acceptability).

Study Timeline

• Study First Submitted: 2014-05-23
• Study First Submitted QC: 2014-05-27
• Study First Posted: 2014-05-28
• Study Start: 2014-08
• Primary Completion: 2016-04
• Study Completion: 2016-04
• Status Verified: 2023-03
• Last Update Submitted: 2023-03-27
• Last Update Posted: 2023-03-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

1. Identify as Puerto Rican or of Puerto Rican descent
2. be able to read Spanish or English
3. currently live in the area and plan to stay until 12 months postpartum
4. be able to participate in Spanish-speaking peer-support group meetings
5. consent to participate
6. pass an informed consent quiz
7. successfully initiate BF
8. be within 15-44 years of age

Exclusion Criteria

1. Have ongoing illicit drug use
2. have current active suicidal thoughts or a past suicide attempt, or a psychiatric hospitalization within the last 3 months
3. have untreated HIV (BF contraindicated)
4. are currently prescribed psychotropic medication (i.e., antidepressants, antipsychotics, mood stabilizers, anxiolytics)
5. have serious postpartum medical problems (e.g., postpartum hemorrhage, infections and serious jaundice requiring exchange transfusion)

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Contingency Management	Contingency Management	These participants will receive usual WIC care. The frequency, duration, content, and size of the meetings and participation requirements will be the same as for the TAU group, except that this group will also receive contingency management (CM). Members will demonstrate breastfeeding and receive cash incentives weekly if they breastfeed.

Primary Outcome Measures

Name	Time	Method
Duration of breastfeeding	6-month postpartum	Observe breastfeeding (BF) behavior looking for one of the following indicators of successful BF in the infant: audible swallowing, a regular suck/swallow/breathe pattern, or visible milk in the infant's mouth after they are not latched anymore. For a mother who pumps milk, observation of pumping combined with observation of the resulting milk being fed to the infant will be observed.

Secondary Outcome Measures

Name	Time	Method
Infant weight	1-month, 3-month, and 6-month postpartum	An infant will be weighed at each assessment time point using a portable Health O Meter Infant Scale.

Trial Locations

Locations (1)

Special Supplemental Nutrition Program for Women, Infants, and Children; 🇺🇸 Philadelphia, Pennsylvania, United States