RecruitingNCT07293559

Understanding Practices of Lactation and Infant Feeding Together With Women With HIV in the United States


Sponsor

International Maternal Pediatric Adolescent AIDS Clinical Trials Group

Enrollment

1,150 participants

Start Date

Feb 24, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

IMPAACT 2046/UPLIFT (Understanding Practices of Lactation and Infant Feeding decisions Together with women with HIV) is a multi-site, mixed-methods, observational cohort study. The purpose of the study is to explore infant feeding preferences, practices, and outcomes among mothers with HIV and their families in the United States. It will employ both qualitative and quantitative research methods to address existing knowledge gaps and to understand the clinical, behavioral, and social factors influencing infant feeding decisions. As part of the study's mixed method approach, a longitudinal cohort study of mothers and their infants will be established. The study also aims to pilot a national registry of breastfeeding women living with HIV in the United States.


Eligibility

Inclusion Criteria26

  • Is of legal age or circumstance to provide independent informed consent
  • Belongs to one of the following five categories:
  • Is pregnant with a gestational age of 28 0/7 to 37 6/7 weeks at entry and is considering breastfeeding
  • Is pregnant with a gestational age of 28 0/7 to 37 6/7 weeks at entry and is not considering breastfeeding
  • Gave birth to a live born infant after 28 February 2023, is over 4 weeks postpartum, did not breastfeed for any duration and has no intent to breastfeed
  • Gave birth to a live born infant after 28 February 2023, is over 4 weeks postpartum, breastfed for less than four weeks, and has weaned
  • Gave birth to a live born infant after 28 February 2023, is over 4 weeks postpartum, and breastfed for four weeks or longer
  • Diagnosed with HIV prior to or during the pregnancy
  • If preferred language is other than English, is willing to participate in interviews with an available translator.
  • Is of legal age or circumstance to provide independent informed consent
  • Is a healthcare provider who self-identifies as an obstetrician, midwife, nurse, adult or pediatric infectious disease specialist, or advance practice provider who participated in the care of at least five PPWH and/or their infants over the three years prior to entry OR
  • Is an ancillary healthcare professional who self-identifies as a social worker, lactation support provider, patient navigator, pharmacist, doula who participated in the care of at least five PPWH and/or their infants over the three years prior to entry
  • Has been identified by a PPWH enrolled in Core Activity 1 as aware of her HIV status and contributing to her infant feeding decisions
  • Is of legal age or circumstance to provide independent informed consent
  • If preferred language is other than English, is willing to participate in interviews with an available translator.
  • Is of legal age or circumstance to provide independent informed consent
  • Is pregnant with singleton fetus with a gestational age of ≥ 28 0/7 weeks at entry OR
  • Gave birth to a live born, singleton infant up to 7 days prior to entry
  • Diagnosed with HIV prior to or during the pregnancy
  • Expected to be available for the duration of follow-up
  • Is of legal age or circumstance to provide independent informed consent
  • Must be up to 7 days postpartum with live-born infant
  • Diagnosed with HIV prior to or during the pregnancy
  • Breastfed her infant for any duration
  • Is of legal age or circumstance to provide independent informed consent
  • Working at a healthcare facility that provides care for women with HIV who are breastfeeding and/or their infants

Exclusion Criteria1

  • Has any condition identified during the screening period that, in the opinion of site investigator, would preclude informed consent, make study participation unsafe, complicate interpretation of study outcome data, or otherwise interfere with achieving the study objectives

Interventions

OTHERNo intervention provided in this study

None; No intervention provided in this study


Locations(11)

University of Southern California (CRS 5048)

Los Angeles, California, United States

David Geffen School of Medicine at UCLA (CRS 5112)

Los Angeles, California, United States

University California, San Diego (CRS 4601)

San Diego, California, United States

University of Colorado, Denver (CRS 5052)

Aurora, Colorado, United States

University of Florida (5051)

Jacksonville, Florida, United States

Univ of Miami Pediatric/Perinatal HIV/AIDS (5127)

Miami, Florida, United States

5030, Emory University School of Medicine Clinical Research Site

Atlanta, Georgia, United States

Lurie Children's Hospital of Chicago (CRS 4001)

Chicago, Illinois, United States

Johns Hopkins University (CRS 5092)

Baltimore, Maryland, United States

Jacobi Med. Ctr. Bronx NICHD CRS (5013)

The Bronx, New York, United States

St. Jude Childrens Research Hosp, Memphis (6501)

Memphis, Tennessee, United States

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NCT07293559


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