N/A
N=7,103
Non-pharmacological Pain Management After Surgery
Surgical Procedure, Unspecified
Bottom Line
View on ClinicalTrials.gov: NCT04570371 ↗Enrolled (actual)
7,103
Serious AEs
0.2%
Results posted
Nov 2025
Primary outcome: Primary: PROMIS-CAT Pain — 59.32; 59.96; 56.94; 56.06 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Conversation Guide + Clinical Support (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Mayo Clinic
- Primary completion
- May 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY PROMIS-CAT Pain |
59.32; 59.96; 56.94; 56.06; 53.08; 53.29 | — |
| PRIMARY PROMIS-CAT Physical Function |
40.50; 39.50; 38.44; 39.68; 42.44; 40.79 | — |
| PRIMARY PROMIS-CAT Anxiety |
50.72; 51.85; 51.93; 51.63; 51.21; 51.75 | — |
| PRIMARY Use of Non-Pharmacological Pain Control Modalities |
23; 752; 58; 2549; 721; 16058 | — |
| PRIMARY Opioid Use |
16158; 26035; 19082; 30414; 22299; 37639 | — |
Summary
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.
Eligibility Criteria
Inclusion Criteria
- All patients 18 years of age and older.
- Must be undergoing qualifying surgeries at participating sites.
- Patients under 18 years of age.
Exclusion Criteria
- Patients under 18 years of age.
Data sourced from ClinicalTrials.gov (NCT04570371). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.