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| ID | Type | Description | Link |
|---|---|---|---|
| R34DA033384 | U.S. NIH Grant/Contract | View source |
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| Name | Class |
|---|---|
| National Institute on Drug Abuse (NIDA) | NIH |
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The proposed research will develop, demonstrate the feasibility of, and pilot test in a randomized controlled trial a prescription opioid taper support intervention. This intervention aims to prevent opioid misuse and adverse events among patients receiving chronic opioid therapy for chronic non-cancer pain without evidence of current substance abuse.
The project will yield information essential to planning a future, larger-scale RCT designed to evaluate: 1) the efficacy of the intervention in preventing prescription opioid abuse, misuse, overdose and other adverse events among patients receiving chronic opioid therapy for chronic non-cancer pain, 2) the effects of the intervention on opioid use, pain, pain related activity interference, and mood. Participants in our pilot study will be limited to those without current opioid abuse or other substance abuse, but past substance abuse will be allowed. This will provide a sample of patients at risk for opioid abuse, misuse and overdose, but who may be able to taper their opioids successfully. Hypothesis: Patients receiving chronic opioid therapy for chronic non-cancer pain who are randomized to the opioid taper support intervention, as compared with patients randomized to usual opioid prescribing care, will have lower opioid average daily doses at 22 and 34 weeks.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| taper support | Experimental | Weekly visits with pharmacological and psychological support for opioid taper at 10% of original dose per week |
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| Usual care | No Intervention | Usual care for chronic pain. All care allowed except buprenorphine. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| opioid taper support | Behavioral | Weekly visits with physician's assistant (supervised by pain physician/psychiatrist and pain psychologist) who provides pharmacological and psychological support for opioid taper at 10% per week |
| Measure | Description | Time Frame |
|---|---|---|
| mean daily opioid dose over past week | mean daily opioid dose over past week as calculated in morphine equivalent dose | week 22 after randomization |
| Measure | Description | Time Frame |
|---|---|---|
| prescription opioid difficulties | Prescription opioid difficulties subscale scores on: psychosocial problems and opioid control concerns | week 22 after randomization |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Washington Center for Pain Relief | Seattle | Washington | 98115 | United States |
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