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临床试验/NCT07631559
NCT07631559尚未招募不适用

Pilot Study of an Adapted Partner Navigation Intervention Booster Session for Sustained Healthcare Engagement Among People Who Inject Drugs

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年9月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
试验地点
1

研究概览

简要总结

This study builds upon an ongoing NIH-funded randomized controlled trial (R01DA053325) evaluating a Partner Navigation Intervention to increase hepatitis C virus (HCV) treatment initiation among young adult people who inject drugs (PWID) and their injecting partners in San Francisco. The proposed research includes secondary analyses of existing trial data, additional survey measures, qualitative interviews, and a pilot intervention adaptation.

The study has two primary objectives. First, it examines how racialized discrimination (structural, interpersonal, and internalized) affects HCV treatment initiation and dyadic partner support processes within injecting partnerships. Second, it evaluates whether a brief, adapted "booster" partner navigation session delivered at HCV treatment completion can improve engagement in ongoing healthcare.

Participants include adults (≥18 years) who inject drugs and have been diagnosed with HCV, along with their primary injecting partners. Study activities include longitudinal surveys, qualitative interviews with a subset of participants, and a pilot intervention session with follow-up evaluation.

This research addresses critical gaps in understanding how social relationships and structural inequities influence healthcare engagement among PWID. Findings will inform culturally responsive adaptations to dyadic interventions and improve continuity of care in a population disproportionately affected by HCV and systemic barriers to healthcare.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

入选标准

  • For index participants:
  • 18 years of age or older at enrollment
  • History of injecting drug use
  • Completed HCV treatment within the past 3 months
  • Report a primary injecting partner willing to participate
  • Willing and able to provide informed consent
  • English or Spanish speaking
  • For primary injecting partners:
  • Primary injecting partner of an enrolled index participant:
  • 18 years of age or older at enrollment
  • Willing and able to provide informed consent
  • English or Spanish speaking
  • has context menu

排除标准

  • For both index participants and injecting partners:
  • Unable to provide informed consent due to cognitive impairment or acute intoxication at the time of enrollment
  • Previously participated in this study in any capacity

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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