Human-centered Injury Thrivorship Pathway for Survivors of Physical Trauma
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Human-Centered Injury Thrivorship Pathway.
- Who it may be relevant to
- Registry conditions: Injury Traumatic, Survivorship, Trauma Injury. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Identifying & Addressing Unmet Needs of Injury Survivors at a Safety Net Hospital in San Francisco
Overview
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.
Interventions
- Other Human-Centered Injury Thrivorship Pathway
Enrollment in the human-centered injury thrivorship pathway.
Primary outcome measures
- Early Implementation Outcomes - Acceptability, Appropriateness, Feasibility [Time frame: 8-12 weeks post-pathway enrollment]
Secondary outcome measures (4)
- Participant pathway resource utilization - type [Time frame: 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 [Time frame: 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 [Time frame: 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 [Time frame: 8-12 weeks post-pathway enrollment plus subsequent time points if continued resource engagement until study completion up to 1 year]
Eligibility criteria
Inclusion criteria
- 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
Exclusion criteria
- Patient < 18 years old
- Deceased during index hospitalization
- Unable to provide informed consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
United States · 1 center
- Zuckerberg San Francisco General Hospital — San Francisco
Publications
- Proctor E, Silmere H, Raghavan R, Hovmand P, Aarons G, Bunger A, Griffey R, Hensley M. Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda. Adm Policy Ment Health. 2011 Mar;38(2):65-76. doi: 10.1007/s10488-010-0319-7. PMID 20957426
Identifiers
NCT: NCT06292039 · P0555788 · 2KL2TR001870