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Completed

NCT Number: NCT03200054

Postpartum Adherence Clubs for Antiretroviral Therapy

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Documented HIV infection with ART initiation during the preceding antenatal period
  • Within 70 days post-delivery
  • Viral suppression documented in pregnancy with the most recent viral load <400 copies/mL within the last 3 months
  • Willingness to be randomised and return for study measurement visits
  • Able and willing to attend service visits at either a local ART treatment centre or the adherence club at Ikhwezi centre
  • Able to provide informed consent for research

Exclusion criteria

  • Intention to relocate out of Cape Town permanently during the study period
  • Any medical, psychiatric or social condition which in the opinion of the investigators would affect the ability to consent and/or participate in the study including: refusal to take ART/antiretrovirals (ARVs) and/or denial of HIV status
  • Loss of pregnancy/neonate at the time of eligibility determination
  • Current co-morbidity requiring additional health care attention, including opportunistic infections such as tuberculosis (TB) disease or any chronic condition or other condition that is not controlled or stable

Treatment and study plan

Adherence Clubs

Other

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.

Primary outcomes

  1. Viral suppression

    Time frame: 24 months

    Time to viral load >1000 copies per ml

Secondary outcomes

  1. Maternal retention in care

    Time frame: 24 months

    Missed routinely scheduled clinical care visits (missed visit and no visit within 3 months of scheduled clinic visit)

  2. Maternal death

    Time frame: 24 months

    Maternal deaths over the study period

  3. Maternal mental health

    Time frame: 24 months

    Mental health as assessed via brief screening tools (Edinburgh Postnatal Depression Scale)

  4. Maternal health care service use

    Time frame: 24 months

    Use of health facilities including hospitalization

  5. Infant death

    Time frame: 24 months

    Infant deaths over the study period

  6. Infant health care service use

    Time frame: 24 months

    Use of health facilities including hospitalization

  7. Infant HIV testing

    Time frame: 24 months

    Uptake of routine infant HIV testing

  8. Infant HIV infection

    Time frame: 24 months

    Mother-to-child transmission of HIV

  9. Infant feeding

    Time frame: 24 months

    Breastfeeding practices

  10. Cost and cost-effectiveness

    Time frame: 24 months

    Cost-effectiveness of each strategy will be analysed from both the patient and health systems perspective

  11. Acceptability of each ART service

    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

  12. Viral suppression at other cutpoints (>400 copies/mL)

    Time frame: 24 months

    Time to VL >400 copies/mL

  13. Viral suppression at other cutpoints (>50 copies/mL)

    Time frame: 24 months

    Time to VL >50 copies/mL

  14. Virologic Failure

    Time frame: 24 months

    Time to clinical definition of virologic failure (two consecutive VLs >1000 copies/mL)

  15. Combined retention/VL outcome

    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)

  16. Viral suppression at each study visit

    Time frame: 24 months

    VL >50 copies/mL or >1000 copies/mL at each study visit (3, 6, 12, 18, 24 months)

Sponsors and collaborators

Lead sponsor

University of Cape Town

Other

Collaborators

  • Medical Research Council

Registry information

Official study title

Postpartum Adherence Clubs for Antiretroviral Therapy: a Randomised Controlled Trial

Acronym: PACART

Important dates

Study start
2016
Primary completion
2020
Study completion
2020
First posted
Jun 27, 2017
Registry last updated
May 18, 2022

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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