Opioid Prescribing Clinical Trial
— POST-OPOfficial title:
Reducing Inappropriate Prescription Opioid Prescribing at Hospital Discharge
Verified date | March 2023 |
Source | RAND |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study tests the effectiveness of two email-based behavioral nudges, one based on peer behavior and one based on best practice guidelines, in reducing excessive opioid prescriptions after surgery. It will be conducted in three surgical specialties (general surgery, orthopedic surgery, and obstetric/gynecological surgery) at 19 hospitals within one healthcare system. These specialties will each be randomized to a control group or one of two nudge groups. Each month for one year, surgeons in the nudge groups will receive emails comparing their opioid prescribing either to their peers' prescribing or to prescribing guidelines. Both types of email-based nudges are expected to reduce opioid prescribing after surgery.
Status | Active, not recruiting |
Enrollment | 778 |
Est. completion date | October 18, 2023 |
Est. primary completion date | October 18, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | The nudges that a surgeon in either intervention arm will receive are based on that surgeon's eligible discharge opioid prescriptions in the previous month. Eligible prescriptions meet all of the following criteria: - the patient is at least 18 years old at the date of surgery - the patient is discharged to their home - the surgical procedure has an applicable post-operative opioid prescribing guideline - the surgical procedure is the only surgical procedure performed during the patient's hospital stay - the prescription is for an opioid taken orally (tablets, capsules, or liquid solution) To avoid contamination between the intervention arms, surgeons who operate across multiple surgical specialties (defined as surgeons who performed less than 90% of their total procedures in one specialty between June 2020 and May 2021) will not be eligible. |
Country | Name | City | State |
---|---|---|---|
United States | Sutter Health | Sacramento | California |
Lead Sponsor | Collaborator |
---|---|
RAND | Sutter Health, University of California, Los Angeles, University of Michigan, University of Southern California |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Share of discharge opioid prescriptions above prescribing guidelines | Prescriptions will be compared to prescribing guidelines via morphine milligram equivalents (MMEs) and coded as within or above guidelines. If no opioid is prescribed at discharge, this will be coded as within guidelines. | 12 months | |
Secondary | Morphine milligram equivalents (MMEs) prescribed at discharge | Continuous measure of the total morphine milligram equivalents prescribed at discharge | 12 months | |
Secondary | Days' supply of opioids prescribed at discharge | Continuous variable indicating the number of days' supply of opioids prescribed at discharge | 12 months | |
Secondary | Share of discharges where any opioid was prescribed | Derived from binary variable indicating if any opioid was prescribed at discharge | 12 months | |
Secondary | Share of patients on opioids for greater than 3 months post-discharge | Derived from binary variable indicating if the patient has any opioid prescriptions between 3 and 6 months after surgery | 3-6 months post-discharge | |
Secondary | Number of 30-day all-cause emergency department visits | Number of emergency department visits the post-operative patient has in the 30 days after the initial procedure | 0-30 days post-discharge | |
Secondary | Number of 30-day all-cause hospitalizations | Number of hospital admissions the post-operative patient has in the 30 days after the initial procedure | 0-30 days post-discharge | |
Secondary | Share of discharge opioid prescriptions above prescribing guidelines in the year after the intervention ends | Prescriptions will be compared to prescribing guidelines via morphine milligram equivalents (MMEs) and coded as within or above guidelines. If no opioid is prescribed at discharge, this will be coded as within guidelines. | 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04509115 -
Variation in Opioid Prescribing and Use for Acute Pain in Diverse Populations
|
||
Completed |
NCT04776928 -
Testing a Provider-Level Feedback Intervention to Optimize Postoperative Prescribing
|
N/A | |
Not yet recruiting |
NCT06443385 -
E-mail Nudges for Prescribing Risky Drugs
|
N/A | |
Completed |
NCT05202795 -
Postpartum Pain Experience and Attitudes About Opioid Prescribing
|
||
Active, not recruiting |
NCT06130904 -
Effect of Academic Detailing on Opioid Prescribing by Dentists to Adolescents and Young Adults
|
N/A | |
Completed |
NCT05299528 -
A Clinician-Focused Nudging Intervention to Optimize Post-Surgical Prescribing
|
N/A | |
Completed |
NCT04425668 -
Effect of Academic Detailing to Reduce Opioid Prescribing in Dentistry
|
N/A |