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Clinical Trials/NCT03986866
NCT03986866
Completed
Not Applicable

Video-based, Patient-Focused Opioid Education in the Perioperative Period: A Feasibility Study

University of Arkansas1 site in 1 country110 target enrollmentApril 29, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Opioid Use
Sponsor
University of Arkansas
Enrollment
110
Locations
1
Primary Endpoint
Knowledge of Post Operative Opioids
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

This is a pilot study designed to assess the feasibility of using a novel, video-based opioid education tool for opioid naïve ambulatory surgery patients in the perioperative period.

Detailed Description

Patients will be randomized to a video or no video prior to surgery then administered a phone questionnaire at post-op day 7, 30, and 90. The Arkansas Prescriptions Drug Monitoring Database will also be accessed for information on opioid prescription refills. The overall goal of the study is to evaluate the effect that video-based opioid education has on narcotic intake after outpatient surgery. The duration of the study will be approximately 3 months, plus a single 1-hour long focus group if desired by the patient.

Registry
clinicaltrials.gov
Start Date
April 29, 2019
End Date
April 1, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Men and women 18 years or older
  • Not chronically receiving opioid analgesics
  • Patients who have not taken opioids 30 days pre-operatively
  • Undergoing surgical procedure not requiring overnight hospital stay

Exclusion Criteria

  • Non-English speaking
  • Legally deaf or blind
  • On opiate contract
  • Has taken oral narcotic in the past 30 days
  • Unable to operate a telephone

Outcomes

Primary Outcomes

Knowledge of Post Operative Opioids

Time Frame: 7 days

Knowledge of Post operative Opioids after surgery via 7 day post operative phone call. Knowledge is measured on a scale of 1 to 10 with 10 being complete knowledge and 1 being no knowledge.

Number of Patients Who Discontinued Opioids by 3 Months

Time Frame: Up to 3 months

Post-operative pain control as determined by opioid utilization at three months. This is the number of patients that have discontinued opioids at the 3 month mark.

Secondary Outcomes

  • Development of Chronic Opioid Use(90-150 days)
  • Number of Total Days to Opioid Cessation(Up to 3 months)

Study Sites (1)

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