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NCT05166356

Determinants and Effects in the Use of NOHARM Pain Management

Describing the Determinants and Effects of Variation in the Adoption and Use of the NOHARM Pain Management Intervention Among Diverse Surgical Practices
Mayo Clinic·ClinicalTrials.govRecruiting
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Study focus
Disease/Condition
Surgical Procedure, Unspecified
Study type
Observational
Sponsor & location
Primary sponsor
Mayo Clinic
Location
Rochester, United States of America
Timeline & enrollment
Phase
N/A
Start date
Mar 01, 2022
End date
Mar 01, 2024
Enrollment
500 participants
Primary outcome

Aim 1,Determinants of patient engagement with the intervention,Sustainability of the NOHARM intervention

Summary

The objective of this study is to enrich the ongoing Non-pharmacological Pain Management
 After Surgery (NOHARM) pragmatic trial (NCT04570371) with a mixed methods analysis of patient
 and care team factors that affect the routine adoption, implementation, and meaningful and
 sustainable use of the NOHARM intervention.

ICD-10 classifications
Surgical procedure, unspecifiedMedical procedure, unspecifiedOther surgical proceduresDuring unspecified surgical and medical careDuring unspecified surgical and medical care
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05166356
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05166356 through Pure Global AI's free database. This phase not specified trial is sponsored by Mayo Clinic and is currently Recruiting. The study focuses on Surgical Procedure, Unspecified. Target enrollment is 500 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.