COMPAS Trial. Collecting Outcomes and Managing Pain After Surgery: Predicting Patients at High Risk for Chronic Opioid Use and Creating Algorithms to Responsibly Tailor Opioid Prescribing and Weaning After Surgery

Duke University

Summary

The primary aim of this study is to measure pain and psychosocial patient reported outcomes, objective functionality, and actual daily at home opioid usage in orthopedic patients. The study's goal following the data collection is to predict which patients are at high risk for chronic opioid use.

Eligibility

Age range: 18–90 years
Sex: All
Healthy volunteers: No

Detailed criteria

Inclusion Criteria: * aged 18-90 years old who are undergoing elective orthopedic surgery at Duke Health. * Patients must have their own smartphone IOS or Android device. * Patients must be able to read English. Exclusion Criteria: * Lacking capacity to provide consent. * Cannot read English * Under 18 years of age * Older than 90 years of age

Interventions

Behavioral
COMPAS Participants
The schedule of events for this study are as follows: Day 1 Pre-Surgery: * Download the Medable App * Register to the study * Validated Questionnaires * Active Task Every Day * 9:00 a.m. Daily Questions * 9:00 p.m. Daily Questions Outcome Surveys and Active Task: * Day 1 Pre-Surgery * 1-Week Post Operation * 2-Weeks Post Operation * 1-Month Post Operation * 3-Months Post Operation * 6-Months Post Operation

Location

Duke Orthopaedics
Durham, North Carolina
neil.d.ray@duke.edu 919-681-1924

COMPAS Trial. Collecting Outcomes and Managing Pain After Surgery: Predicting Patients at High Risk for Chronic Opioid Use and Creating Algorithms to Responsibly Tailor Opioid Prescribing and Weaning After Surgery

Summary

Eligibility

Interventions

Location

Run this study?

Details

Conditions