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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04336592
Other study ID # 20-001864
Secondary ID UG3AG067593
Status Completed
Phase
First received
Last updated
Start date May 13, 2020
Est. completion date February 28, 2021

Study information

Verified date August 2021
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Researchers are promoting non-pharmacological pain management strategies for patients by assisting them in identifying post-surgical pain care preference following an operative procedure at Mayo Clinic.


Description:

This is a pilot study to test promoting non-pharmacological pain management strategies for patients by assisting them in identifying post-surgical pain care preference following an operative procedure. This pilot study will confirm the feasibility of patient-facing as well as clinician-facing decision support components of an electronic health record (EHR) imbedded evidence-based bundle.


Recruitment information / eligibility

Status Completed
Enrollment 128
Est. completion date February 28, 2021
Est. primary completion date February 28, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients scheduled to receive a surgical spine procedure at Mayo Clinic - Surgeons, Physician pain specialists and allied health caring for patients meeting patient inclusion criteria Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms

  • Non-Pharmacological Pain Management

Intervention

Behavioral:
Non-pharmacological Options in post-operative Hospital and Rehabilitative Management (NOHARM)
Gathers patient preferences for non-pharmacological pain management strategies through medical record and inform clinicians (via prompts, orders, etc.) of these preferences and encourages conversation about these preferences throughout their routine pre- and post-surgical interactions with patients. Resources will be provided to bedside clinicians as they assist patients in identifying a personalized post-discharge pain management strategy.

Locations

Country Name City State
United States Mayo Clinic Health System - Eau Claire Eau Claire Wisconsin
United States Mayo Clinic Florida Jacksonville Florida
United States Mayo Clinic Health System - Franciscan Healthcare La Crosse Wisconsin
United States Mayo Clinic Health System in Mankato Mankato Minnesota
United States Mayo Clinic in Rochester Rochester Minnesota
United States Mayo Clinic in Arizona Scottsdale Arizona

Sponsors (2)

Lead Sponsor Collaborator
Mayo Clinic National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Non-Pharmacological options participation Number of participants to complete the non-pharmacological options in post-operative Hospital and Rehabilitative Management 1 month post-operative

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