No intervention provided in this study
OtherNone; No intervention provided in this study
NCT Number: NCT07293559
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.
Interested in participating?
Request InfoAll sexes
Observational
David Geffen School of Medicine at UCLA (CRS 5112), Los Angeles, California, United States
This is a convergent mixed-method, multisite study to identify factors in infant feeding decisions and explore infant feeding perspectives, preferences, practices and outcomes among women with HIV in the US. Feasibility and acceptability of developing a national registry of breastfeeding women with HIV in the US will also be assessed. The study sites will enroll women with HIV who are pregnant or postpartum (PPWH), healthcare providers (HCPs) and ancillary healthcare professionals (AHPs), other influential individuals who contribute to infant feeding decisions, and pilot registry testers.
The study will be comprised of three core activities:
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Core Activity 1 Inclusion Criteria: Pregnant and Postpartum Women with HIV
Core Activity 1 Inclusion Criteria: Healthcare Providers and Ancillary Healthcare Professionals
Core Activity 1 Inclusion Criteria: Influential Individuals
Core Activity 2 Inclusion Criteria: Pregnant and Postpartum Women with HIV and their Infant
Core Activity 3 Inclusion Criteria: Breastfeeding Postpartum Women with HIV and their Infant
Core Activity 3 Inclusion Criteria: Pilot Registry Testers
Exclusion criteria
Core Activities 1-3
None; No intervention provided in this study
Time frame: Within 28 days and 2 years of Enrollment
Qualitative themes from in-depth interviews
Time frame: Monthly, through study completion, up until 5 years
Binomial outcome from site level surveys
Time frame: At 48 weeks post birth
Binary outcome
Time frame: At 48 weeks post birth
Binary outcome
Time frame: Through 96 weeks post birth
Numerical outcome
Time frame: Through 96 weeks post birth
Binary outcome
Time frame: At 48 weeks post birth
Descriptive joint display table, with qualitative key themes and quantitative findings
Time frame: Through 48 weeks post birth; At weaning up to 96 weeks post birth
Binary outcome
Time frame: Through 48 weeks post birth; At weaning up to 96 weeks post birth
Numerical outcome
Time frame: Through study completion, an average of 3 years
Binary outcome; whether specified percentage of data is completed in registry
Time frame: Through study completion, an average of 3 years
Numerical outcome
Time frame: Through study completion, an average of 3 years
Binary outcome; whether sites complete entries
Time frame: Within 28 days and 2 years of Enrollment
Qualitative themes from in-depth interviews
Time frame: Monthly, through study completion, up to 5 years
Site surveys, provider surveys, In-depth Interviews
Time frame: Through study completion, up to 5 years
Numerical outcome, by feeding approach
Time frame: Through study completion, up to 5 years
Numerical outcome
Time frame: Through study completion, up to 5 years
Numerical outcome
Time frame: At 20 Weeks, At 48 Weeks
Numerical outcome, by infant feeding method
Time frame: At 20 weeks, At 48 weeks
Numerical outcome, by infant feeding method
Time frame: Through study completion, up to 96 weeks post birth
Binary outcome, by infant feeding method
Time frame: At 20 weeks, At 48 weeks
Numerical outcome
Time frame: At 20 weeks, At 48 weeks
Ordinal outcome
Time frame: Through 48 weeks post birth, At weaning up to 96 weeks post birth
Numerical outcome and categorical outcome
Time frame: Through 48 weeks post birth, At weaning up to 96 weeks post birth
Numerical outcome
Contact information is provided by the study sponsor or research team.
International Maternal Pediatric Adolescent AIDS Clinical Trials Group
Network
Acronym: UPLIFT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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