跳至主要内容
临床试验/NCT06292039
NCT06292039尚未招募不适用

Identifying & Addressing Unmet Needs of Injury Survivors at a Safety Net Hospital in San Francisco

University of California, San Francisco2 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2027年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
25
试验地点
2
主要终点
Early Implementation Outcomes - Acceptability, Appropriateness, Feasibility

研究概览

简要总结

The goal of this clinical trial is to pilot and evaluate a human-centered injury thrivorship pathway in injury survivors. The main question it aims to answer is:

• Is the pathway appropriate, acceptable, and feasible to meet the medical and social needs of injury survivors?

Injury survivors will be purposively sampled to enroll in the pathway and asked to participate in in-depth interviews and their use of pathway resources will be tracked.

研究设计

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

  • Patient ≥ 18 years old presenting with a physical injury to Zuckerberg San Francisco General Hospital
  • Admitted to the hospital ≥ 24 hours
  • Discharged from the hospital alive
  • San Francisco resident or unhoused in San Francisco
  • Capacity for informed consent

排除标准

  • Patient < 18 years old
  • Deceased during index hospitalization
  • Unable to provide informed consent

研究组 & 干预措施

Injury Thrivorship Pathway

Experimental

Enrollment in the human-centered injury thrivorship pathway.

干预措施: Human-Centered Injury Thrivorship Pathway (Other)

结局指标

主要结局

Early Implementation Outcomes - Acceptability, Appropriateness, Feasibility

时间窗: 8-12 weeks post-pathway enrollment

Early implementation outcomes will be assessed via purposive sampling of pathway participants, their caregivers, and trauma care stakeholders for in-depth semi-structured interviews. "Acceptability is the perception among implementation stakeholders that a given treatment, service, practice, or innovation is agreeable, palatable, or satisfactory. Appropriateness is the perceived fit, relevance, or compatibility of the innovation or evidence based practice for a given practice setting, provider, or consumer; and/or perceived fit of the innovation to address a particular issue or problem. Feasibility is defined as the extent to which a new treatment, or an innovation, can be successfully used or carried out within a given agency or setting."

次要结局

  • Participant pathway resource utilization - type(8-12 weeks post-pathway enrollment plus subsequent time points if continued resource engagement until study completion up to 1 year)
  • Participant pathway resource utilization - frequency(8-12 weeks post-pathway enrollment plus subsequent time points if continued resource engagement until study completion up to 1 year)
  • Participant pathway resource utilization - % utilized(8-12 weeks post-pathway enrollment plus subsequent time points if continued resource engagement until study completion up to 1 year)
  • Participant pathway resource utilization - duration(8-12 weeks post-pathway enrollment plus subsequent time points if continued resource engagement until study completion up to 1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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