RECRUITING

The Implementation of a Post-operative Communication App to Improve Pain Control and Opioid Use

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Digital communication tools are becoming ubiquitous in healthcare, though their impact on patient/provider communication, healthcare utilization, and outcomes remains poorly established. M Health Fairview (MHFV) in collaboration with the Center for Learning Health System Sciences (CLHSS) Rapid Eval team will be evaluating one such communication application: OPY, which leverages the Epic-Care Companion functionality to remove barriers in communicating with the patient's care team. This project will evaluate the effectiveness of a digital, post-operative patient engagement tool (Epic-Care Companion made available through MyChart), OPY, which has the goal of preventing patients from becoming addicted to opioids or to suffer from opioid misuse or diversion. In the proposed pragmatic trial, standard care with education available in MyChart and the patient after visit summary will be augmented by OPY. OPY is available to patients starting the same day they go home from surgery with a new opioid prescription. OPY provides a daily interactive experience that collects patient pain and side-effect information, provides advice for pain management, and uses behavioral "nudges" to encourage timely weaning and responsible disposal of opioid medications. The primary goal of this project is to evaluate the effect of two versions of OPY on measures of opiate use relative to the standard of care in a pragmatic randomized controlled trial.

Official Title

The Implementation of a Post-operative Communication App to Improve Pain Control and Opioid Use

Quick Facts

Study Start:2024-07-17
Study Completion:2026-07-17
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06124079

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Surgery at The M Health Fairview Clinics and Surgery Center - Maple Grove (Maple Grove) or M Health Fairview Clinics and Surgery Center - Minneapolis (CSC)
  2. * Active opioid prescription (prescribed between 30 days prior to surgery, until day of surgery)
  3. * Patient class (outpatient or same day surgery)
  4. * Never previously randomized or exposed to OPY
  1. * Age \< 18
  2. * Chronic opiate use defined as:
  3. * Patients aged 18 and older and
  4. * 3 or more opioid dispensing events, in the last 12 months with at least 1 of these events in the last 6 months.
  5. * Any long acting opioid prescription in the last 6 months
  6. * Interpreter needed - YES selected (EPT840)
  7. * Patient has a Health Proxy (Legal Guardian) designated in Epic
  8. * Patients who have opted out of clinical research
  9. * Patients with an active palliative care referral

Contacts and Locations

Study Contact

Maya Peters
CONTACT
612-790-0401
mayap@umn.edu

Principal Investigator

Genevieve Melton-Meaux, PhD
PRINCIPAL_INVESTIGATOR
University of Minnesota

Study Locations (Sites)

University of Minnesota
Minneapolis, Minnesota, 55414
United States

Collaborators and Investigators

Sponsor: University of Minnesota

  • Genevieve Melton-Meaux, PhD, PRINCIPAL_INVESTIGATOR, University of Minnesota

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-17
Study Completion Date2026-07-17

Study Record Updates

Study Start Date2024-07-17
Study Completion Date2026-07-17

Terms related to this study

Additional Relevant MeSH Terms

  • Acute Pain