CompletedNot Applicable

Determinants and Effects in the Use of NOHARM Pain Management

United States372 participantsStarted 2022-03-01

Plain-language 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.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Participants eligible for this study will be patients on the NOHARM trial registry (e.g., patients that were automatically assigned to receive the NOHARM intervention as part of their surgical care) and/or their charts and members of their care teams, including nurses, doctors, physical therapists, nurse practitioners and physician assistants, and medical assistants. Exclusion Criteria: * Individuals not on the NOHARM trial registry.

What they're measuring

Aim 1

Timeframe: 3 months post-surgery

Determinants of patient engagement with the intervention

Timeframe: 3 months post-surgery

Sustainability of the NOHARM intervention

Timeframe: 3 months post-surgery

Trial details

NCT IDNCT05166356

SponsorMayo Clinic

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-02-01

View on ClinicalTrials.gov More Surgical Procedure, Unspecified trials