Gugulethu Community Health Centre
Cape Town, Western Cape, 7750, South Africa
NCT Number: NCT03200054
South Africa is implementing the policy of universal initiation of lifelong antiretroviral therapy (ART) in all HIV-infected pregnant women regardless of CD4 cell count or disease stage ("Option B+"). There is a recognised need for innovative models of service delivery to support adherence and retention in care in this group, particularly during the postpartum period. The investigators are conducting a pragmatic randomised control trial to compare virological outcomes 24 months postpartum in two models of service delivery for provision of HIV care and treatment services postpartum in women who initiated ART during pregnancy: local adult ART clinics and community-based adherence clubs.
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Female
Interventional
Not applicable
Cape Town, Western Cape, 7750, South Africa
South Africa is implementing the policy of universal initiation of lifelong ART in all HIV-infected pregnant women regardless of CD4 cell count or disease stage ("Option B+") and given the high antenatal HIV seroprevalence, HIV-infected pregnant women represent the largest group of patients initiating ART in primary care facilities. However, there are few well developed models of service delivery to support implementation. There are particular concerns regarding the postpartum period, with multiple studies indicating high levels of non-retention in care and/or inadequate adherence to treatment postnatally. Adherence Clubs (ACs) are an innovative but untested model of care based on chronic disease management strategies that emphasize social support, adherence to treatment and retention in care, rather than intensive clinical management, as the most important determinant of long-term health outcomes in stable patients in chronic care. ACs have preliminarily been shown to to result in virologic outcomes that are similar to routine clinic services in patients stable on ART. The investigators are conducting a pragmatic, randomised controlled trial to evaluate two different strategies for delivering HIV care and treatment services during the postpartum period to HIV-infected women who initiated ART during pregnancy. Participants will be allocated to receive ART care at either local adult ART clinics, following the current standard of care, or the community-based adherence club system.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Women will be referred to the ACs at their postpartum ART clinic visit at the midwife obstetric unit (MOU) at the Gugulethu community health centre (CHC). AC visits occur 2-4 monthly at a community hall near the CHC. At routine visits, which last ~1 hour, community health workers provide health education, weigh participants, ask about symptoms, and dispense pre-packed ART. Symptomatic participants are referred back to the main ART facility at the CHC for assessment by a nurse. A nurse performs routine phlebotomy at an annual club visit, and does a clinical assessment and reviews blood results at the subsequent visit. Participants requiring more regular follow-up and those with raised viral loads are referred back to the ART clinic at the CHC by the nurse.
Time frame: 24 months
Time to viral load >1000 copies per ml
Time frame: 24 months
Missed routinely scheduled clinical care visits (missed visit and no visit within 3 months of scheduled clinic visit)
Time frame: 24 months
Maternal deaths over the study period
Time frame: 24 months
Mental health as assessed via brief screening tools (Edinburgh Postnatal Depression Scale)
Time frame: 24 months
Use of health facilities including hospitalization
Time frame: 24 months
Infant deaths over the study period
Time frame: 24 months
Use of health facilities including hospitalization
Time frame: 24 months
Uptake of routine infant HIV testing
Time frame: 24 months
Mother-to-child transmission of HIV
Time frame: 24 months
Breastfeeding practices
Time frame: 24 months
Cost-effectiveness of each strategy will be analysed from both the patient and health systems perspective
Time frame: 24 months
Acceptability of each service will be assessed using the patient-provider interview schedule, and qualitative interviews will be done on a subset of participants
Time frame: 24 months
Time to VL >400 copies/mL
Time frame: 24 months
Time to VL >50 copies/mL
Time frame: 24 months
Time to clinical definition of virologic failure (two consecutive VLs >1000 copies/mL)
Time frame: 24 months
Composite endpoint of retention in care and viral suppression (not retained in care OR retained but VL >50 or 1000 copies/mL)
Time frame: 24 months
VL >50 copies/mL or >1000 copies/mL at each study visit (3, 6, 12, 18, 24 months)
University of Cape Town
Other
Postpartum Adherence Clubs for Antiretroviral Therapy: a Randomised Controlled Trial
Acronym: PACART
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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