Opioid Use, Unspecified Clinical Trial
Official title:
Prescribing Opioid Pain Relievers in the Emergency Department: Understanding and Optimizing the Encounter
NCT number | NCT02299024 |
Other study ID # | SP0017808 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 2012 |
Est. completion date | May 2013 |
Verified date | August 2019 |
Source | Northwestern University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators overall study objective is to improve patients knowledge and safe use of opioid pain relievers upon discharge from the Emergency Department.
Status | Completed |
Enrollment | 278 |
Est. completion date | May 2013 |
Est. primary completion date | May 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - prescribed an opioid pain reliever - English Speaking Exclusion Criteria: - Non-English Speaking - Clinically unstable, psychologically impaired or intoxicated as judged by the research staff member. - Chronic opioid use, defined as daily or near daily use of opioid pain relievers for the past 90 days. - admitted to hospital - unable to complete follow up phone interview in 4 - 7 days. |
Country | Name | City | State |
---|---|---|---|
United States | Northwestern University | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Northwestern University | Emergency Medicine Foundation |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Knowledge of medication name | The primary outcome was the patients ability to identify the medication name of their prescribed opioid pain reliever upon follow-up. | 4-7 days | |
Secondary | Knowledge and counseling recall outcomes | In addition to the outcome of medication name patients were asked additional knowledge and recall questions including: active ingredients in the medication, knowledge about safe daily dose of acetaminophen, side effects, recall of counseling about activities to avoid (drinking alcohol, driving vehicle), knowledge about addictive potential of the medication. | 4-7 days | |
Secondary | Actual Use outcomes | Patients were queried about their home use of the medication including: pain score at home, average number of tabs per day, and satisfaction with pain reduction. Additionally they were asked about the timing of any alcohol consumption or driving in relation to the timing of medication dosing. | 4-7 days | |
Secondary | Response to the intervention | Patients in the intervention arm were asked how they liked the intervention using a series of question with a Likert scale. | 4-7 days |
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