CompletedNot Applicable

Non-pharmacological Pain Management After Surgery

United States81,938 participantsStarted 2020-10-16

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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

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.

What they're measuring

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

Trial details

NCT IDNCT04570371

SponsorMayo Clinic

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-05-02

Results submitted2025-09-25

View on ClinicalTrials.gov More Surgical Procedure, Unspecified trials