The purpose of this study is to test the impact of a bundled NOHARM Conversation Guide with clinical decision support intervention embedded within an Electronic Health Record (EHR) on pain and function 3 months following surgery.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
PROMIS-CAT Pain
Timeframe: Baseline (before hospital discharge), 1-,2-, and 3-Months Post-Surgery
PROMIS-CAT Physical Function
Timeframe: Baseline (before hospital discharge), 1-,2-, and 3-Months Post-Surgery
PROMIS-CAT Anxiety
Timeframe: Baseline (before hospital discharge), 3-Months Post-Surgery
Use of Non-Pharmacological Pain Control Modalities
Timeframe: 3 Months Post-Surgery
Opioid Use
Timeframe: 3-Months Post-Surgery