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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
10,000
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
Duke Orthopaedics
Durham, North Carolina, United States
RECRUITINGReported Pain of Participants measured via PROMIS-29
28 Questions regarding pain are ranked on a 5-point Likert Scale with 1 meaning "not at all" and 5 meaning "very much".
Time frame: 6 Months
Reported Pain of Participants measured via PROMIS-29
One question on an 11-point rating scale for pain intensity, with 0 meaning "no pain" and 10 meaning "worst imaginable pain".
Time frame: 6 Months
Reported Pain of Participants measured via Pain Catastrophizing pain scale.
Statements regarding pain are rated on a scale from 0 to 4 with 0 meaning "not at all" and 4 meaning "all the time"
Time frame: 6 Months
Opioid Use of Participants
Total number of patients with self reported use of opioids.
Time frame: 6 months
Practicality of Mobile Application
How long participants actively use the app to track their opined use and pain.
Time frame: 6 Months
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