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临床试验/NCT01810289
NCT01810289已完成不适用

The "START" (a Streamlined ART Initiation Strategy) Study

University of California, San Francisco0 个研究点目标入组 12,024 人开始时间: 2013年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
12,024
主要终点
Cumulative Incidence of ART Initiation 14 Days After Clinical Eligibility in Treatment Eligible HIV-infected Patients

研究概览

简要总结

START is clinic-level (not individual-patient) intervention to catalyze the process of ART initiation among HIV-infected adults who meet CD4-based criteria for combination ART (e.g., adults with a CD4 T cell level < 350/ul). The three START components are: (1) real-time point-of-care CD4 testing using the Alere PIMA platform to ascertain treatment eligibility in real time at first presentation to care, (2) targeted knowledge transfer (i.e., dissemination) of recent scientific evidence regarding effects rapid ART initiation on survival to front line health care workers; and 3) feedback and reporting to clinic and providers. There three components represent empirically validated steps in the PRECEED implementation model.

详细描述

RATIONALE: In Africa, up to a 50-75% of HIV-infected, adults fail to initiate (FTI) ART or encounter delays of months even after eligibility through CD4+ T-cell testing or clinical criteria are established. Recent randomized trials including ACTG Protocol 5164, ACTG 5221, CAMELIA and SAPIT have demonstrated that delays of even weeks in ART initiation increases mortality among patients presenting with active opportunistic infections. Even among those without active infections, mortality among untreated persons with a CD4 < 350 approaches 15/100 person-years - a large proportion of which should be avoidable in patients who have presented to care. New dissemination and implementation strategies that are generalizable across resource-limited settings are needed to address FTI and make the public health approach more effective. The overall goal of the multi-component START strategy is to initiate the greatest number of eligible patients in the shortest amount of time possible, while maintaining safety, efficacy and cost effectiveness.

HYPOTHESIS: The START intervention, a combined intervention using provider education, novel technology and reinforcing feedback, will increase the rapidity and completeness of ART initiation.

INTERVENTION: START is clinic-level (not individual-patient) intervention to catalyze the process of ART initiation among HIV-infected adults who meet CD4-based criteria for combination ART (e.g., adults with a CD4 T cell level < 350/ul). The three START components are: (1) real-time point-of-care CD4 testing using the Alere PIMA platform to ascertain treatment eligibility in real time at first presentation to care, (2) targeted knowledge transfer (i.e., dissemination) of recent scientific evidence regarding effects rapid ART initiation on survival to front line health care workers; and 3) feedback and reporting to clinic and providers. There three components represent empirically validated steps in the PRECEED implementation model.

STUDY DESIGN: A cluster-randomized, step-wedge trail of 20 clinics operated by the Makerere Joint AIDS Program. Four clinic sites will be randomly assigned to the START at 6-month intervals between month six and 24 during the three-year trial.

PRIMARY OBJECTIVE

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All MJAP-supported clinics in Kampala and Mbarara Districts

排除标准

  • 未提供

研究组 & 干预措施

MJAP Clinics Intervention

Experimental

START intervention. This is a stepped wedge design so each clinic will experience both conditions.

干预措施: START (Behavioral)

MJAP Clinics Pre-Intervention

No Intervention

Standard of care. This is a stepped wedge design so each clinic will experience both conditions.

结局指标

主要结局

Cumulative Incidence of ART Initiation 14 Days After Clinical Eligibility in Treatment Eligible HIV-infected Patients

时间窗: 14 days

Patients may be ART eligible at the start of the study or become ART eligible for the first time in the 3 year time frame.

次要结局

  • Retention in HIV Care Among Treatment-eligible, HIV-infected Patients.(1 years)
  • HIV RNA Levels Among Treatment-eligible, HIV-infected Patients One Year Following ART Eligibility(1 year)
  • Incidence of Vertical Transmission in All HIV-infected Women Who Are Treatment-eligible During the Study Period.(3 years)
  • Incidence of Mortality in Treatment-eligible, HIV-infected Patients.(1 years)

研究者

申办方类型
Other
责任方
Sponsor

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