RecruitingNot Applicable

Collecting Outcomes and Managing Pain After Surgery

United States10,000 participantsStarted 2025-01-13

Plain-language 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.

Who can participate

Age range18 Years – 90 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

Reported Pain of Participants measured via PROMIS-29

Timeframe: 6 Months

Reported Pain of Participants measured via PROMIS-29

Timeframe: 6 Months

Reported Pain of Participants measured via Pain Catastrophizing pain scale.

Timeframe: 6 Months

Opioid Use of Participants

Timeframe: 6 months

Practicality of Mobile Application

Timeframe: 6 Months

Trial details

NCT IDNCT03834818

SponsorDuke University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2028-04

Contact for this trial

Ashley Burke

+1 919 681 2849 ashley.burke@duke.edu

View on ClinicalTrials.gov More Surgery trials