Comparative Effectiveness Trial of Communication Strategies in the Management of Chronic Pain
Chronic Pain
About this trial
This is an interventional health services research trial for Chronic Pain focused on measuring Clinical Decision Support, Patient Education Materials, Opioid Use, Chronic Noncancer Pain
Eligibility Criteria
Inclusion Criteria:
Within a 90-day period prior to the patient recruitment date:
- ≥30 days of prescriptions for opioid medications; or
- 2 or more opioid prescriptions; or
- a total amount of ≥700 Morphine Milligram Equivalents (MME) in a single opioid prescription;
and
- Patients who have had 1 or more Cedars-Sinai Medical Group primary care physician in the year prior to the study start date; and
- At least 1 visit during the follow-up year (the follow-up year will start after they consent to be in the study).
Prescriptions in the inpatient setting will not make a patient eligible for this study.
Exclusion Criteria:
- Individuals less than 18 years of age; or
- Individuals with any cancer treatment (chemotherapy or radiotherapy) administered 180 days or less prior to patient recruitment; or
- Individuals with a cancer diagnosis in the Problem List 180 days or less prior to patient recruitment (patients with cancer surveillance only will be included in the study); or
- Individuals with palliative care treatment administered 180 days or less prior to patient recruitment; or
- Individuals with any end-of-life treatment (comfort care) prior to patient recruitment; or
- Patients currently taking prescription medications (e.g. Suboxone, subutex, Buprenex, Butrans, Probuphine, Belbuca, buprenorphine/naloxone, Zubsolv, and Bunavail) for Opioid Use or other Substance Use Disorder treatment.
Sites / Locations
- Cedars-Sinai Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Clinical Decision Support
Patient Education and Activation Tools
Patients within the physicians randomized to the IDM arm will receive the Clinical Decision Support alerts via the EHR when certain order criteria are triggered appropriately.
Patients within the physicians randomized to SDM will receive the PEAT materials via REDCap two days prior to their PCP office visit. They will receive these materials every time they have an office visit with their PCP.