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| ID | Type | Description | Link |
|---|---|---|---|
| 2KL2TR001870 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Center for Advancing Translational Sciences (NCATS) | NIH |
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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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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Injury Thrivorship Pathway | Experimental | Enrollment in the human-centered injury thrivorship pathway. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Human-Centered Injury Thrivorship Pathway | Other | Enrollment in the human-centered injury thrivorship pathway. |
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| Measure | Description | Time Frame |
|---|---|---|
| Early Implementation Outcomes - Acceptability, Appropriateness, Feasibility | 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." | 8-12 weeks post-pathway enrollment |
| Measure | Description | Time Frame |
|---|---|---|
| Participant pathway resource utilization - type | Participant engagement with applicable pathway resources will be tracked by type of resource(s) accessed | 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Marissa A Boeck, MD, MPH | Contact | 415-502-4745 | marissa.boeck@ucsf.edu |
| Name | Affiliation | Role |
|---|---|---|
| Marissa A Boeck, MD, MPH | University of California, San Francisco | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Zuckerberg San Francisco General Hospital | San Francisco | California | 94110 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 20957426 | Background | 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. |
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The investigators are undecided how individual participant data will be shared with other researchers, which the investigators will update prior to the initial recruitment date. The primary outcome will be qualitative data from in-depth semi-structured interviews linked to participant demographic and clinical information. The secondary outcome will be quantitative based on resource utilization, also linked to participant demographic and clinical information.
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| ID | Term |
|---|---|
| D014947 | Wounds and Injuries |
| D000081084 | Accidental Injuries |
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Participant engagement with applicable pathway resources will be tracked by frequency of use of the resource(s) |
| 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 | Participant engagement with applicable pathway resources will be tracked by duration of use of the resource(s) | 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 | Participant engagement with applicable pathway resources will be tracked by overall % of resources utilized out of resource(s) offered | 8-12 weeks post-pathway enrollment plus subsequent time points if continued resource engagement until study completion up to 1 year |