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Clinical Trials/NCT03012087
NCT03012087
Completed
N/A

Using m-Health Tools to Reduce the Misuse of Opioid Pain Relievers

Johns Hopkins Bloomberg School of Public Health2 sites in 1 country123 target enrollmentSeptember 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prescription Drug Abuse
Sponsor
Johns Hopkins Bloomberg School of Public Health
Enrollment
123
Locations
2
Primary Endpoint
Change in Self-Reported Preference for Opioid Pain Reliever
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of this study is to pilot test a web-based, patient-centered educational program that encourages the patient to have an informed discussion about pain medication options with their emergency department (ED) provider.

Detailed Description

This multi-site, randomized trial will evaluate an m-health program designed to aid the patient in making an informed decision about their pain treatment. Patients reporting to the ED with an injury-related chief complaint who agree to participate are randomized to receive the intervention program, My Healthy Choices, or an attention-matched control. My Healthy Choices pairs tailored education with a patient decision aid to describe what opioid and non-opioid pain medications are, assess the patient's risk factors for opioid-related adverse effects, and produce a tailored report that patients are encouraged to share with their doctor. Data are collected through surveys at three time points during the ED encounter (baseline, immediately after the intervention, and just before discharge), and at a 6-week follow-up survey. The primary outcomes are whether the patient prefers an opioid pain reliever (OPR) and whether the patient takes an OPR. The investigators hope this program will facilitate patient-provider communication, as well as reduce the number of prescriptions written for OPRs and thus the number of patients exposed to prescription opioids and the associated risks of addiction and overdose.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
June 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • ED visit for an injury- or pain-related chief complaint
  • 18 years of age or older
  • speak English
  • has a smart phone or email address that is used on a regular basis
  • no previous medical care for the current complaint
  • triage pain score between 7-10

Exclusion Criteria

  • allergy to pain medications
  • have used a prescription pain medication for more than two days in the past month
  • report renal problems or a history of dialysis

Outcomes

Primary Outcomes

Change in Self-Reported Preference for Opioid Pain Reliever

Time Frame: Baseline and Immediate Post-test

Assessed via questionnaire on a scale of 0-10.

Secondary Outcomes

  • Change in Knowledge about Prescription Pain Medication Side Effects and Safe Practices for Taking, Storing and Disposing Prescription Pain Medications(Baseline and 6 weeks)
  • Self-Reported Prescription Drug Storage and Disposal Behaviors(6 weeks)

Study Sites (2)

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