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Идёт набор NCT06493357

Evaluation of a Differentiated Point-of-care Active Case Finding & Management Model to Eliminate Mother-to-Child Transmission of HIV in Malawi

Без фазы С лечением HIV Prevention

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: PAC-Man, Standard of Care.
Кому может быть актуально
Состояния в реестре: HIV Prevention. Базовые параметры: от 16 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Malawi
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

UNCPM 22401 - Evaluation of a Differentiated Point-of-care Active Case Finding & Management Model for the Elimination of Mother-to-Child Transmission of HIV in Lilongwe and Mangochi, Malawi

Обзор

Purpose: To conduct a hybrid effectiveness-implementation stepped-wedge trial to: 1. Estimate the effect of the PAC-Man model, compared to SOC, on the proportion of infants who receive timely EID testing. 2. Estimate the effect of the PAC-Man model, compared to SOC, on the proportion of pregnant and breastfeeding women living with HIV who receive guideline-adherent viral load testing. 3. Compare implementation outcomes between the PAC-Man model and SOC. Participants: The total study sample size is 2,426, including 2,304 mother-infant pair (MIP) survey participants, 48 high-risk pregnant/breastfeeding women living with HIV for in-depth interviews (from high-risk MIPs who participated in a survey); 10 PMTCT policy makers and Ministry of Health (MOH)/ President's Emergency Plan for AIDS Relief (PEPFAR) implementing partner senior managers for key informant interviews; and about 48-64 professional and lay health providers for focus group discussions and implementation actor surveys. To rigorously evaluate the PAC-Man model, investigators will use a hybrid (type 3) effectiveness-implementation incomplete stepped-wedge trial design. The hybrid incomplete stepped-wedge design is a rigorous quasi-experimental design that allows for incremental "rollout" of the PAC-Man model and serial measurement of both health outcomes (for infants and mothers in Objectives 1 and 2, respectively), as well as implementation outcomes (Objective 3). The incomplete stepped-wedge design is more efficient than a complete design, minimizes costs, and reduces participant burden, without sacrificing statistical precision. Using this design, sequential crossover from control (i.e., the SOC) to intervention (i.e., SOC plus the PAC-Man model) takes place at each 'step' using cluster randomization until all clusters (defined as a group of "sites," or health facilities plus the surrounding communities in its catchment area) receive the intervention. The 12 sites included in our study will be divided into 4 clusters of 3 sites each.

Подробное описание

PAC-Man Model:

PAC-Man represents an integrated differentiated services delivery (DSD) model for mothers and infants that brings the following three evidence-based practices into the community for elimination of mother to child transmission (EMTCT): 1) pediatric active case finding using novel point-of-care (POC) early infant diagnosis (EID) technology; 2) same-day antiretroviral therapy (ART) initiation for infants newly diagnosed with HIV infection; and 3) maternal viral load (mVL) testing and back-to-care services. PAC-Man uses a mobile approach to offer EMTCT services in the community and reach "high risk" MIPs in which the mother living with HIV did not initiate ART, started ART late during pregnancy or breastfeeding, dropped off treatment following ART initiation, was unsuppressed on ART, was identified with HIV infection for the first-time during the post-partum period, and/or did not return with her infant for EID testing. Because these evidence-based practices are already recommended by the Ministry of Health and will be functioning at the site and not the individual level, delivering the PAC-Man model will be done under the auspices of routine care, applying an overarching implementation strategy of creating new mobile care teams equipped with new diagnostic technology who deploy the m-PIMA™ in community settings.

PAC-Man Implementation Approaches:

The overall implementation strategy being evaluated in this study is the creation of mobile care teams to deploy m-PIMA™ and provide EMTCT services in the community. Complementing this overarching strategy will be two sub-strategies used to enhance PAC-Man adoption: 1) task shifting of active case finding, EID and mVL testing, ART initiation, and back-to-care services to community health workers (CHWs), community nurses, and HIV diagnostic assistants; and 2) changing service sites to convenient locations in the community to overcome barriers to EID and mVL delivery. These strategies are intended to work in concert with the above evidence-based practices to integrate PAC-Man into the EMTCT program.

Вмешательства

  • Поведенческое PAC-Man
    PAC-Man represents an integrated DSD model for mothers and infants that brings the following three evidence-based practices into the community for EMTCT: 1) pediatric active case finding using novel POC EID technology; 2) same-day ART initiation for infants newly diagnosed with HIV infection; and 3) mVL testing and back-to-care services. PAC-Man uses a mobile approach to offer EMTCT services in the community and reach "high risk" MIPs. Delivering the PAC-Man model will be done under the auspices
  • Поведенческое Standard of Care
    Routine care as provided by Ministry of Health.

Первичные конечные точки

  • Proportion of infants who receive EID testing by age 6 months [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
Вторичные конечные точки (12)
  • Proportion of infants who receive EID testing by age 2 months [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of infants who receive EID testing by age 12 months [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of high-risk infants who receive EID testing by age 6 months [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of infants who initiate ART [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Median infant results return time [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of infants newly diagnosed with HIV [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Median age at ART initiation among infants [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Median time to ART initiation among infants [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of infants who initiate ART the same day as diagnosis [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of infants with HIV retained in care at 3 months post-ART initiation [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of infants with HIV retained in care at 6 months post-ART initiation [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]
  • Proportion of MIPs reached with viral load testing [Срок оценки: Within 12 months of MIP enrollment in the national EMTCT program]

Критерии участия

The criteria for Enumerated MIP Cohort is as follows:

Критерии включения

  • Enrolled in the national EMTCT program at a study site in the 12 months preceding a survey.

Критерии исключения

  • None.

The criteria for Enumerated MIP Field Survey is as follows:

Критерии включения

  • Age 16 years or older.
  • Enrolled in the national EMTCT program at a study site in the 12 months preceding a survey.

Критерии исключения

  • Documented transferred out from a site prior to the field survey.
  • Participated previously in the field survey.
  • Decline informed consent.

The criteria for In-Depth Interviews is as follows:

Критерии включения

  • Age 16 years or older.
  • Met high-risk criteria for PAC-Man model.
  • Participated in a field survey.

Критерии исключения

  • Decline informed consent.

The criteria for Focus Group Discussions is as follows:

Критерии включения

  • Age 18 years or older.
  • MOH or implementing partner professional or lay health worker at a study site (such as nurses, community health workers, health surveillance assistants, and HIV diagnostic assistants)
  • Generally familiar with the PAC-Man model and/or EMTCT/ EID service delivery at their site.

Критерии исключения

  • Decline informed consent.

The criteria for Key Informant Interviews is as follows:

Критерии включения

  • Age 18 years or older.
  • HIV/ EMTCT policy maker OR MOH/ PEPFAR implementing partner senior manager.
  • Generally familiar with HIV and/or EMTCT/ EID service delivery.

Критерии исключения

  • Decline informed consent.

The criteria for Implementation Actor Questionnaires is as follows:

Критерии включения

  • Age 18 years or older.
  • Professional or lay health provider at a study site.
  • Generally familiar with HIV and/or EMTCT/ EID service delivery at their site.
  • Participated in a focus group discussion.

Критерии исключения

  • Decline informed consent.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

Malawi · 3 центра
  • Bwaila Hospital — Lilongwe
  • Area 18 Health Centre — Lilongwe
  • Monkey Bay Community Hospital — Monkey Bay

Публикации

  • Herce ME, Cassidy C, Munson A, Edwards JK, Rutstein SE, Matoga M, Kumwenda C, Simon KR, van Oosterhout JJ, Cox CM, Kamanga F, Kumwenda W, Phiri S, Rambiki E, Thawani A, Huwa J, Malewezi B, Mvalo T, Bula A, Chinula L, Hoffman I, Squibb MA, Nyirenda RK, Saidi F, Hosseinipour MC, Chagomerana MB. Study design and procedures for a hybrid effectiveness-implementation incomplete stepped-wedge cluster-ran PMID 40721832

Идентификаторы

NCT: NCT06493357 · 24-0561 · 1P01HD112215

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗