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OpenTrials
Completed

NCT Number: NCT02491177

Mother and Infant Visit Adherence and Treatment Engagement Study

This is a 2x2 factorial cluster randomized trial of two interventions to improve retention and adherence for women and infants on Option B+. The overall goal is to determine which intervention (or combination of interventions) maximizes antiretroviral therapy (ART) adherence and retention in care in the context of Option B+ and thus improves maternal and infant health outcomes.The proposed study will be conducted in rural Nyanza Province, Kenya at 20 low-resource primary health care facilities and associated communities supported by Family AIDS Care and Education Services (FACES), a President's Emergency Plan for AIDS Relief (PEPFAR)-funded HIV prevention care, and treatment program, ((AIDS) acquired immune deficiency syndrome, (HIV) human immunodeficiency virus) . The investigators will assess both process and outcome indicators using a 2x2 factorial design, in which equal numbers of clusters will be randomized to one of the interventions (community-based mentor mothers or theory-based mobile text messages), both interventions, or standard of care. The interventions will be added to fully integrated high quality HIV and antenatal, maternal, neonatal, and child health (ANC/MNCH) services already offered at these sites.

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Key information

About this study

In order to eliminate new pediatric HIV infections, save maternal lives, and simplify antiretroviral therapy (ART) implementation in settings with generalized HIV epidemics, current World Health Organization (WHO) guidance recommends lifelong triple ART for all pregnant and breastfeeding women (Option B+). However, despite the promise of Option B+ to remove logistical barriers and to promote maternal health through life-long ART, this strategy brings challenges. Key amongst these challenges are adherence to ART and continuous retention in HIV care, especially for women who do not require ART for their own health. Barriers to adherence and retention in care for prevention of mother-to-child transmission (PMTCT) have been identified at the individual, interpersonal, community, and health facility levels; yet specific barriers in the context of Option B+ are not well understood. The investigators' study will be conducted at 20 health facilities and associated communities in Nyanza Province, Kenya where Mother to Child Transmission (MTCT) rates prior to Option B+ roll-out remained near 10%, despite the wide availability of PMTCT services. As Option B+ is scaled up in Kenya, it is essential to identify effective methods to ensure long-term adherence and retention in care for mother-baby pairs, throughout pregnancy, breastfeeding, and beyond. Building on the investigating team's prior research experience in this setting, the investigators propose to gain understanding of and address potential barriers at the individual, community, and health facility levels through formative research with HIV-positive pregnant and postpartum women, their male partners, and health care providers. This information will be used to refine two proposed interventions that are highly likely to maximize ART adherence and retention in care among HIV-infected pregnant women and HIV-exposed infants. These interventions will be rigorously tested in rural Kenya, using a cluster randomized 2x2 factorial design. The evidence-based interventions to be tested will include 1) community Mentor Mothers (cMM) who will provide support for ART adherence and retention in care for HIV-positive women in the community and 2) individually tailored, theory based mobile phone text messages to help retain women and infants in HIV care. The investigators' overall goal is to determine which intervention (or combination of interventions) maximizes ART adherence and retention in care in the context of Option B+ and thus improves maternal and infant health outcomes. The investigators' primary outcomes will include ART adherence at 12 months postpartum and retention in care, measured by a documented HIV care visit within 90 days prior to 12 months postpartum. Secondary outcomes will include MTCT at 6 weeks, 12 months and 18 months; as well as maternal viral loads and CD4 counts. Results from this study will inform the scale-up of Option B+ in Kenya by identifying effective interventions and combinations of interventions that can reduce barriers and increase facilitators of optimal ART adherence and retention in care with the aims of reaching the elimination of mother to child transmission of HIV and significantly improving maternal health.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 years or older,
  • HIV-infected pregnant women and their HIV-exposed infants pairs,
  • attends the antenatal care (ANC) clinic at one of the study sites.

Exclusion criteria

  • Less than 18 years of age,
  • HIV-infected women not currently pregnant,
  • not HIV-infected at the time of the first ANC visit.

Treatment and study plan

cMM

Behavioral

Home visits from community mentor mothers

Text messaging

Behavioral

Text messages received on mobile phone

Primary outcomes

  1. Self-reported adherence on antiretroviral therapy

    Time frame: 12 months post-partum

    Self-report

  2. Adherence on antiretroviral therapy

    Time frame: 12 months post-partum

    Viral load<100 copies/ml based on medical records

  3. Adherence on antiretroviral therapy (infant)

    Time frame: 12 months post-partum

    Use of ARVs for the infant

  4. Retention in care

    Time frame: 12 months post-partum

    Proportion of women who have an HIV care visit within 90 days at 12 months after the birth

  5. Adherence on antiretroviral therapy (dried blood spots)

    Time frame: 12 months post-partum

    Viral load<100 copies/ml based on dried blood spots

Secondary outcomes

  1. Maternal CD4 count change

    Time frame: 6 months after baseline

    Change in CD4 count baseline to 6 months after baseline

  2. Maternal viral load count change

    Time frame: 6 months after baseline

    Change in viral load from baseline to 6 months after baseline

  3. Infant retention in care (feeding method)

    Time frame: 12 and 18 months

    Infant feeding method

  4. Infant retention in care

    Time frame: 12 and 18 months

    Retention in care through 12 and 18 months

  5. Infant retention in care (survival status)

    Time frame: 12 and 18 months

    Survival status of infant

  6. Uptake of intervention services (Number/types of text messages sent)

    Time frame: 3 years

    Number/types of text messages sent

  7. Uptake of intervention services (receipt of text messages)

    Time frame: 3 years

    Receipt of text messages

  8. Uptake of intervention services (home visits)

    Time frame: 3 years

    Number of home visits received

  9. Uptake of intervention services (support groups attended)

    Time frame: 3 years

    Number of support groups attended.

  10. Mother-to-Child-Transmission

    Time frame: 6 weeks, 9 months and 18 months

    Result of infant HIV test at 6 wks, 9,18 months

  11. Infant testing

    Time frame: 6 weeks, 9 months and 18 months

    Uptake and date of infant testing

  12. Infant enrollment in care

    Time frame: 6 weeks

    Infant enrollment in HIV care

  13. Male partner involvement

    Time frame: 12 months post-partum

    Composite variable including Y/N response to indicate if male partner attended a health visit with his female partner, encouraged facility delivery, reminded to take HIV medication, reminded to go for HIV care, provided transport money to go to the clinic/dispensary, reminded to give the infant prophylaxis, helped giving the infant prophylaxis medication, collected medication for the woman or infant, encouraged specific infant feeding, and encouraged pediatric HIV testing. These are assessed in the follow-up questionnaires completed at 12 months post-partum.

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • Kenya Medical Research Institute
  • University of Alabama at Birmingham

Registry information

Official study title

Maximizing Adherence and Retention for Women and Infants in the Context of Option B+

Acronym: MOTIVATE!

Important dates

Study start
2014
Primary completion
2019
Study completion
2021
First posted
Jul 7, 2015
Registry last updated
Apr 26, 2021

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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