A Study Of Parallel Data-Stream Integration During Simulated Clinical Care

Overview

About this study

The purpose of this study is to demonstrate continuous, valid multi-parameter Omni capture during both scenarios, including scenario-critical channels.

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. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria: Clinicians

  • Age 18 years or older.

  • Employed, credentialed, or training at Mayo Clinic in an eligible clinical role.

  • Able to understand the study procedures and provide informed consent.

  • Able to participate in an English-language simulation and interview.

  • For Scenario 1, able to use translated communication with a standardized patient as part of the simulation.

Exclusion Criteria: Clinicians

  • Unable or unwilling to provide informed consent or be video/audio recorded.

  • Directly supervised by a member of the recruitment or consent team when the relationship could reasonably create undue influence unless an IRB-approved independent recruitment process is used.

  • Prior involvement in developing the exact scripted answer key when participation would compromise blinded performance assessment unless participation is limited to non-scored pilot testing.

Inclusion Criteria: Standardized Patients

  • Age 18 years or older.

  • Be an experienced standardized patient (actor) available to portray scripted clinical scenarios.

  • Be able to follow standardized simulation scripts and study procedures.

  • Able to provide informed consent and tolerate wearing the noninvasive devices for the planned session.

  • For Scenario 1, bilingual proficiency in the selected Spanish and English sufficient to deliver and verify the scripted content.


Exclusion Criteria Standardized Patients

  • Unable or unwilling to be video/audio recorded.

  • Skin condition, allergy, implanted device, or other circumstance identified by the device instructions as incompatible with the wearable sensors.

  • Any discomfort or safety concern identified before or during device placement.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 07/27/2026. Questions regarding updates should be directed to the study team contact.

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

Jacksonville, Fla.

Mayo Clinic principal investigator

Christopher McLeod, M.B., Ch.B., Ph.D.

Open for enrollment

Contact information:

Laura Pacheco-Spann

9049530408

pachecospann.laura@mayo.edu

More information

Publications

Publications are currently not available