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| ID | Type | Description | Link |
|---|---|---|---|
| R01HS027790 | U.S. AHRQ Grant/Contract | View source |
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| Name | Class |
|---|---|
| University of Arkansas | OTHER |
| University of Washington | OTHER |
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Because of recent policies to decrease opioid use, some people using long-term opioid therapy (LTOT) are encouraged or required to stop (discontinue) taking opioids. That has led experts to be concerned that patients whose LTOT is discontinued could have untreated pain, turn to other substance use and possibly illicit opioids, or have worsened mental health symptoms leading to suicide. To guide safer policies, guidelines, and care, this study will interview patients and doctors about discontinuing LTOT and use the results to develop a patient-centered decision aid (DA) to improve patient-provider communication around discontinuation of LTOT. Once the DA is finalized, it will be pilot tested with a group of 30 patients who are currently on LTOT. The pilot will assess DA implementation feasibility; acceptability; knowledge transfer; and ability to successfully foster positive, patient-centered conversations about opioid discontinuation.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Decision Aid Pilot Test | Experimental |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Patient-centered Decision Aid to support long-term opioid therapy tapering | Behavioral | Earlier aims of this study developed a patient-centered Decision Aid (DA) that uses stories of people who benefited from discontinuing and clear explanations of evidence for key choices to decrease stigma; empower patients; increase engagement and productive interaction with providers in decision making; and reduce fear, anger and anxiety about tapering. The DA will be designed to support conversations that providers often find challenging and help providers maintain patient trust and satisfaction. Participants in the pilot test will be asked to: 1) complete a pre-DA survey, 2) review the DA, 3) have a guided conversation with a trained study interventionist with a behavioral health background who is trained on how to use the DA, and 4) complete a post-DA survey. |
| Measure | Description | Time Frame |
|---|---|---|
| Acceptability of DA | We will use Matlock et al.'s acceptability ranking scale to assess the acceptability of the DA to patients | 1-2 weeks |
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EHR-based inclusion criteria:
Inclusion criteria confirmed by participant
EHR-based exclusion criteria:
Exclusion criteria determined by study
- participated in an interview for Aim 1 of this study
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| Name | Affiliation | Role |
|---|---|---|
| Clarissa W Hsu, PhD | Kaiser Permanente | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Kaiser Permanente Washington Health Research Institute | Seattle | Washington | 98101 | United States |
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| ID | Term |
|---|---|
| D059350 | Chronic Pain |
| ID | Term |
|---|---|
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
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