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Increase Breastfeeding Duration Among Puerto Rican Mothers (BFCM)

T

Treatment Research Institute

Status

Completed

Conditions

Breastfeeding

Treatments

Behavioral: Contingency Management

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02148237
R03HD077057
1R03HD077057-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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).

Full 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).

Enrollment

60 patients

Sex

Female

Ages

15 to 44 years old

Volunteers

Accepts Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Treatment as Usual
No Intervention group
Description:
Participants in Treatment as Usual (TAU) will receive standard breastfeeding (BF) services from the WIC program and participate in research assessments. Standard services include an on-site and home-visiting lactation consultant, occasional one-on-one peer counseling, and an enhanced food package for BF women.
Contingency Management
Experimental group
Description:
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.
Treatment:
Behavioral: Contingency Management

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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