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Evaluation of Clinical Decision Support in Opioid Tapering

Evaluation of Clinical Decision Support in Opioid Tapering

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06527079
Enrollment
200000
Registered
2024-07-30
Start date
2026-08-01
Completion date
2027-06-01
Last updated
2026-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Harm Reduction, Medication Abuse, Opioid Overdose, Opioid Prescribing, Opioid Use Disorder, Prevention

Brief summary

The 2022 Center for Disease Control and Prevention (CDC) clinical practice guideline for prescribing opioids for pain recommends that when tapering a patient's opioid dose, doses should be decreased at a slow rate to reduce the risk of withdrawal symptoms, overdose, and to promote tolerance of the tapering. This project will evaluate a clinical decision support (CDS) tool in the form of a clinical care pathway that gives providers information, recommendations, and educational material on strategies for opioid tapering. Primary care providers will be randomized at the clinic location to a control arm or intervention arm. The control arm will have the clinical care pathway available, but will not be reminded of the pathway when tapering a patient. The intervention arm will receive a nudge when prescribing a tapering opioid strategy to a patient to use the clinical care pathway. The rate of opioid tapering in line with CDC guidelines will be examined as well as long-term patient outcomes of opioid overdose or poisoning using existing patient health records. The study period will be approximately 18 months.

Interventions

OTHEROpioid Tapering Pathway Clinical Decision Support (CDS)

Clinical decision support in the form of an electronic health record (EHR)-integrated, provider facing notification suggesting the provider utilize a clinical care pathway that provides resources and decision support in opioid tapering in line with CDC guidelines.

Sponsors

University of Colorado, Denver
Lead SponsorOTHER
National Institute on Drug Abuse (NIDA)
CollaboratorNIH
National Institutes of Health (NIH)
CollaboratorNIH

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to 89 Years
Healthy volunteers
Yes

Inclusion criteria

Primary care patients being tapered from an opioid. Tapering patients: * Have an active opioid prescription for more than 3 months and * Prescribed more than 90 morphine milligram equivalents (MME) per day or * Co-prescribed an opioid and benzodiazepine or * Received a reduction in opioid dosage by more than 5% MME per day

Exclusion criteria

* Patients \<12 and \>89 * Patients with active cancer diagnosis in last 1 year * Patients with hospice care/palliative care order * Patients with sickle cell disease diagnosis

Design outcomes

Primary

MeasureTime frameDescription
Percentage of encounters tapering within CDC guidelines18 monthsThe number of encounters where a provider's actions are in line with CDC tapering guidelines divided by the total number of opioid tapering prescriptions

Secondary

MeasureTime frameDescription
Clinical decision support (CDS) acceptance rate18 monthsThe number of times providers accepted the clinical decision support (CDS) tool and utilized the clinical care pathway
Subsequent opioid overdose/poisoning rates6 months after taper encounterThe number of patients who had a diagnosis of opioid overdose or poisoning in the six months following an opioid tapering prescription
Health care utilization6 months after taper encounterThe number of emergency department and clinic visits

Contacts

CONTACTHeather Tolle, PhD
heather.tolle@cuanschutz.edu303-724-9924
PRINCIPAL_INVESTIGATORJason Hoppe, DO

University of Colorado, Denver

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 24, 2026