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NCT Number: NCT06292039

Human-centered Injury Thrivorship Pathway for Survivors of Physical Trauma

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.

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Key information

Conditions

Injury Traumatic Accidental Injuries Survivorship Trauma Injury Wounds and Injuries

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Zuckerberg San Francisco General Hospital

San Francisco, California, 94110, United States

Location contact

Marissa A Boeck, MD, MPH

CONTACT

[email protected]

415-502-4745

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Human-Centered Injury Thrivorship Pathway

Other

Enrollment in the human-centered injury thrivorship pathway.

Primary outcomes

  1. Early Implementation Outcomes - Acceptability, Appropriateness, Feasibility

    Time frame: 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."

Secondary outcomes

  1. 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 engagement with applicable pathway resources will be tracked by type of resource(s) accessed

  2. 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 engagement with applicable pathway resources will be tracked by frequency of use of the resource(s)

  3. 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 engagement with applicable pathway resources will be tracked by duration of use of the resource(s)

  4. 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

    Participant engagement with applicable pathway resources will be tracked by overall % of resources utilized out of resource(s) offered

Study contacts

Contact information is provided by the study sponsor or research team.

Marissa A Boeck, MD, MPH

CONTACT

[email protected]

415-502-4745

Sponsors and collaborators

Lead sponsor

University of California, San Francisco

Other

Collaborators

  • National Center for Advancing Translational Sciences (NCATS)

Registry information

Official study title

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

Important dates

Study start
2027
Primary completion
2027
Study completion
2027
First posted
Mar 4, 2024
Registry last updated
May 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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