跳至主要内容
临床试验/NCT06730555
NCT06730555招募中不适用

Project ACCESS: Advancing Access to HIV/HCV Testing Through Transformation in Syringe Services Programs: A Cluster Randomized Trial

University of Miami1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年6月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Number of SSP participants reached

研究概览

简要总结

The purpose of this study is to test the effectiveness of the ACCESS strategy: an organizational-level intervention that uses funding and practice facilitation to improve the organizational capacity of syringe services programs (SSPs) to implement routine, opt-out HIV and Hepatitis C (HCV) testing and linkage to care for people who inject drugs (PWID).

研究设计

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

入排标准

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

入选标准

  • •SSPs must:
  • •be operating in an Ending the HIV Epidemic (EHE) or Centers for Disease Control and Prevention (CDC) determined vulnerable jurisdictions;
  • •serve at least 300 unique participants per year;
  • •not currently offer opt-out HIV/HCV testing;
  • •be capable and willing to prospectively collect aggregated, site-level data on the number of participants who are: i) offered HIV/HCV screening, ii) completed these tests, and iii) linked to care, as well as provide participant demographics;
  • •have key staff that consent to participate in study surveys, qualitative interviews and practice facilitation throughout the study.

排除标准

  • •SSPs must not:
  • •currently receive or have received Frontline Communities in the United States (FOCUS) funding;
  • •have already implemented opt-out HIV/HCV testing.
  • •currently participating in SAIA-SSP-HIV (NCT06025435)

研究组 & 干预措施

ACCESS Group

Experimental

Participants in this group will receive the ACCESS intervention for up to 18 months

干预措施: ACCESS Intervention (Behavioral)

Control Group

Active Comparator

Participants in this group will receive a link to the CDC Compendium of Evidence-Based Interventions for up to 18 months.

干预措施: Control Group (Behavioral)

结局指标

主要结局

Number of SSP participants reached

时间窗: up to 18 months

Number of total HIV/HCV tests completed divided by the number of unique individuals seen

Adoption

时间窗: up to 6 months

Proportion of SSPs that have created an HIV/HCV opt-out testing policy

次要结局

  • Number of SSP participants reached after the intervention(up to 30 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tyler Scott Bartholomew

Associate Professor

University of Miami

研究点 (1)

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