HIV and AIDS Trial, Recruiting

Written by an AI model from ClinicalTrials.gov eligibility criteria and checked on a sample basis. Please confirm against the original criteria.

Who might be able to join this trial:

This trial has several different groups of participants. People who meet the criteria for one of the following groups may be considered:

Group 1 – Pregnant or postpartum women living with HIV (Core Activity 1):

• People who are old enough and legally able to give their own consent to participate
• People who fall into one of these situations: currently pregnant (between 28 and 37 weeks along) and thinking about breastfeeding; currently pregnant (between 28 and 37 weeks along) and not planning to breastfeed; gave birth to a live baby after 28 February 2023, are more than 4 weeks postpartum, and did not breastfeed and do not plan to; gave birth to a live baby after 28 February 2023, are more than 4 weeks postpartum, breastfed for less than four weeks, and have stopped; or gave birth to a live baby after 28 February 2023, are more than 4 weeks postpartum, and breastfed for four weeks or longer
• People who were diagnosed with HIV before or during their pregnancy
• People whose main language is not English and who are willing to take part in interviews with the help of an available translator

Group 2 – Healthcare providers and related professionals (Core Activity 1):

• People who are old enough and legally able to give their own consent to participate
• Healthcare providers who identify as an obstetrician, midwife, nurse, infectious disease specialist (adult or paediatric), or advanced practice provider, and who were involved in the care of at least five pregnant or postpartum women with HIV and/or their babies in the three years before joining the trial
• Professionals in supporting roles — such as social workers, lactation support providers, patient navigators, pharmacists, or doulas — who were involved in the care of at least five pregnant or postpartum women with HIV and/or their babies in the three years before joining the trial

Group 3 – Influential individuals (Core Activity 1):

• People who have been identified by an enrolled pregnant or postpartum woman with HIV as someone who knows about her HIV status and has played a role in her infant feeding decisions
• People who are old enough and legally able to give their own consent to participate
• People whose main language is not English and who are willing to take part in interviews with the help of an available translator

Group 4 – Pregnant or postpartum women with HIV and their baby (Core Activity 2):

• People who are old enough and legally able to give their own consent to participate
• People who are pregnant with a single baby at 28 weeks or more, or who gave birth to a single live baby up to 7 days before joining the trial
• People who were diagnosed with HIV before or during their pregnancy
• People who are expected to be available for the full follow-up period of the study

Group 5 – Breastfeeding postpartum women with HIV and their baby (Core Activity 3):

• People who are old enough and legally able to give their own consent to participate
• People who are up to 7 days postpartum with a live-born baby
• People who were diagnosed with HIV before or during their pregnancy
• People who breastfed their baby for any length of time

Group 6 – Pilot registry testers (Core Activity 3):

• People who are old enough and legally able to give their own consent to participate
• People who work at a healthcare facility that provides care for women with HIV who are breastfeeding and/or their babies

Who may not be able to join:

• People who have any condition identified during the screening period that, in the opinion of the trial site investigator, would prevent them from giving informed consent, make participation unsafe, make study results harder to interpret, or otherwise interfere with the goals of the study

Important: Always verify eligibility with the trial site directly before applying.