A Study to Evaluate Non-pharmacological Options in Postoperative, Hospital-based Rehabilitation Pain Management

Overview

About this study

The purpose of this study is to confirm the feasibility of each component of the Non-pharmacological Options in postoperative Hospital-based And Rehabilitation pain Management (NOHARM) research strategy.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:

  • Adults, 18 years or older.
  • All patients scheduled for a qualifying surgery throughout Mayo Clinic Rochester.

Exclusion Criteria:

  • Lack of English fluency.
  • Member of a vulnerable population (prisoner)
  • Dementia, severe hearing or visual impairment, intellectual disabilities.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jon Tilburt, M.D.

Open for enrollment

Contact information:

Amanda Nelson

(507)422-6252

Nelson.Amanda2@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20469838

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