Support for people recovering from opioid overdoses in Seattle
Official title: Overdose Recovery and Care Access (ORCA) Qualitative Stakeholder Interviews and County-level Data
Run by University of Washington · NCT06768814 · Data updated 2026-11-12
This study tests a new support center for people recovering from opioid overdoses in Seattle to see if it helps them get better care and stay safe compared to those who don’t use the center.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 40000 (estimated) |
| Sponsor | University of Washington Academic / other |
| Locations | 1 site (Seattle, Washington) |
| Status | Recruiting |
| Started | December 15, 2024 |
| Main results expected | May 31, 2028 |
| Study ends | May 31, 2029 |
| Registry record updated | May 6, 2026 |
| Trial ID | NCT06768814 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older who have experienced or are at high risk for opioid overdose and are willing to consent to transfer of care to the SASC.
✕Probably not a fit
Patients who are not experiencing an opioid overdose or do not meet the clinical inclusion criteria will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates a new sub-acute stabilization center (SASC) designed for individuals who have experienced or are at risk of opioid overdoses. Participants will be referred by Seattle Fire Department emergency medical services and will receive comprehensive care, including monitoring, medication-assisted treatment, and linkage to ongoing support services. The study will compare outcomes for those who utilize the SASC with those who do not, using data from EMS records and stakeholder interviews to assess implementation and effectiveness.
Why it matters
Potential benefit: If successful, this initiative could significantly improve recovery outcomes and access to care for individuals affected by opioid use disorder.
How similar studies have gone: Other studies have shown promise in similar approaches to overdose recovery and harm reduction, indicating potential for success in this intervention.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Verbally consents to transfer of care to SASC. 2. Awake and oriented to person and place, with no significant deficits in mental status or neurological function. 3. Age \>=18 4. Patent airway and effective respirations with adequate oxygenation. 5. Stable heart rate and blood pressure, with no evidence of cardiac arrhythmias or other significant cardiovascular disfunction. 6. Vitals: * Heart rate: 45-130 * Blood pressure: systolic 95-190, diastolic 50-120 * Respiratory rate: 10-24 * SpO2: \>92 on room air or supplemental O2 via nasal cannula. * SpO2 \<92% with supplemental O2 requires ED transfer. * EtCO2: \<50 * Temperature: 95.5-100.3 F * Blood glucose (if indicated): 60-300 7. No signs of head trauma: * Dizziness or loss of balance * Blurred vision or double vision * Sensitivity to light or noise * Seizures or convulsions * Weakness or numbness in the arms or legs * Persistent or worsening headache * CSF or blood leaking from the nose or ears * Unequal pupils or pupils that are slow to react to light. 8. No signs of other traumatic injury or medical needs requiring immediate treatment. 9. No signs of respiratory infection. Screen for COVID-19. See COVID-19 Screening protocol. Exclusion Criteria: \- People under 18 and who do not meet SASC admission criteria will be excluded.
Where it's running
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Downtown Emergency Service Center's Overdose Recovery and Care Access Centers
Seattle, Washington, United States Recruiting
Study contacts
- Principal investigator: Caleb Banta-Green, PhD, MPH, MSW — University of Washington
- Study coordinator: Anthony S Floyd, PhD
- Email: asfloyd@uw.edu
- Phone: 206-616-7382
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Non-invasive treatment for opioid withdrawal using vagal nerve stimulation
This study is testing whether a non-invasive treatment using Vagal Nerve Stimulation can help people with opioid use disorders feel better during withdrawal and reduce cravings.
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Community-based program for youth with opioid use disorder
This study is testing a community program that helps young people with opioid use disorder get better treatment and support to see if it keeps them engaged in recovery and reduces overdoses.
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CBD for Opioid Dependence and Pain on Buprenorphine
This study tests whether different doses of cannabidiol (CBD) can affect pain and opioid cravings in adults with opioid use disorder who are on buprenorphine, using a short, randomized, placebo-controlled setup.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.