Mode
Text Size
Log in / Sign up
N/A N=652 Randomized Health Services Research

EHR-Based Medication Complete Communication Strategy to Promote Safe Opioid Use

Opioid Use, Unspecified

Enrolled (actual)
652
Serious AEs
0.0%
Results posted
Sep 2019
Primary outcome: Primary: Safe Medication Dosing (Prescription Understanding) — 0.67; 0.83; 0.79 probability

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
EMC2 Strategy (Behavioral); SMS Text Reminders (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
Aug 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Safe Medication Dosing (Prescription Understanding)
0.67; 0.83; 0.79
SECONDARY
Medication Knowledge
5.48; 5.46; 6.06
SECONDARY
Proper Medication Use (Medication Diary)
0.52; 0.66; 0.65
SECONDARY
Current Opioid Misuse Measure (COMM)
0.70; 0.78; 0.71
SECONDARY
Pain Score
2.76; 2.47; 2.60

Summary

The purpose of this study is to test the effectiveness of an electronic health record based strategy in promoting safe use of opioid medications after an Emergency Department (ED) visit. The electronic health record (EHR)-based strategy was designed to enhance provider counseling about opioids and to standardize and simplify the information that patients receive.

Eligibility Criteria

Inclusion Criteria

  • To be eligible to enroll and remain in the study, patient subjects must meet all of the following criteria:
  • Patient age 18 years and older
  • English language speaking
  • prescribed pill form of hydrocodone-acetaminophen opioid pain reliever
  • own a cell phone with text messaging capabilities
  • the patient is the person primarily responsible for administering medication

Exclusion Criteria

  • Subjects will be excluded from the study if any of the following conditions are met:
  • Aged <18
  • non-English speaking
  • clinically unstable, psychologically impaired or intoxicated as judged by research staff member or emergency physician
  • 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 interviews
  • pregnant
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02431793). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search