Collecting Outcomes and Managing Pain After Surgery (COMPAS)

Duke University

Status: Enrolling

Conditions: Surgery

Treatments: Behavioral: COMPAS Participants

Study type: Interventional

Funder types: Other

Identifiers

NCT03834818

Pro00094157

Details and patient eligibility

About

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.

Enrollment: 10,000 estimated patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

10,000 participants in 1 patient group

COMPAS Participants

Experimental group

Description:

Patents between the ages of 18 and 90 who are undergoing orthopedic surgery at Duke Health will be eligible for enrollment.

Treatment:

Behavioral: COMPAS Participants