Evaluation of Clinical Decision Support in Opioid Tapering

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age12-89
SponsorUniversity of Colorado, Denver

About this trial

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 examine the state of tapering in primary care across the system as well as conduct stakeholder interviews to understand the resources available across the system to support providers in tapering and identify opportunities for clinical decision support to be implemented to support guideline concordant tapering. Utilization of a clinical care pathway that gives providers information, recommendations, and educational material on strategies for opioid tapering will be examined. The rate of opioid tapering in line with CDC guidelines will be examined as well as long term patient outcomes of opioid overdose of poisoning using existing patient health records. The study period will be approximately 8 months.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial population

Residents and visitors to the state of Colorado who seek healthcare within the University of Colorado Health (UCHealth) primary care system receiving long-term opioid treatment.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

  • Observational study without a prospective intervention

    Other intervention

    observational study without a prospective intervention

Treatment groups

200,000 Participants
are divided into 1 treatment group
Group A: Usual Care1 intervention

Trial outcomes

Primary outcomes

1

Percentage of potential taper-benefit patients

The percentage of chronic opioid primary care patients for which EHR risk indicates tapering may be beneficial

Time frame
8 months

Secondary outcomes

1

Observed tapering

The percentage of primary care patients with sustained opioid morphine milligram equivalence (MME) rates declining monthly as an indication of tapering

Time frame
8 months
2

Taper magnitude

The percentage of primary care patients with sustained opioid morphine milligram equivalence (MME) rates declining monthly at a rate in line with guideline recommendations

Time frame
8 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Colorado, Denver

Lead sponsor

National Institute on Drug Abuse (NIDA)

Collaborator

National Institutes of Health (NIH)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: