Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Illinois Chicago
Age
Any age
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Minors and/or Special-needs patients who are scheduled for standard clinical care with a participating student during the study period may be enrolled as secondary subjects provided that their parent/guardian or legally authorized representative (LAR) grants permission during the consent process and the patient assents to the research when appropriate.
Adult Patients with capacity who are scheduled for standard clinical care with a participating student during the study period may be enrolled as secondary subjects provided that are willing to provide informed consent.
Willing to allow an observer and collection of minimal visit-level variables (behavior/cooperation score, sedation status, broad procedure category).
Patients and/or their parent(s), guardian(s), or legally authorized representative(s) providing consent must be able to understand and communicate in English.
You may not be if
Not assigned to patient-care rotations during the study window.
Known dermatologic, cardiovascular, neurologic, or other medical conditions that would interfere with safe or accurate HR monitoring or tolerability of a wrist device.
Unwilling or unable to provide consent or follow procedures.
Declines consent/permission/assent or withdraws at any time.
Prisoners or individuals under custodial supervision.
Pregnant women
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