Wearable Technology in Endoscopy

Mayo Clinic292 enrolled

Overview

Researchers are assessing the accuracy and safety of wearable technology in subjects undergoing endoscopic gastrointestinal procedures with sedation.

This is a prospective, non-blinded, exploratory study to assess the accuracy and safety of wearable devices in the endoscopy suite with patients undergoing procedures using anesthesia assisted sedation using smart watches. We will also simultaneously perform an assessment of patient and provider preferences using narrative-driven, qualitative evaluation.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

292

Conditions

Healthy

Interventions

Consumer-facing wearable smart watchDEVICE

Wearable watch technology that has the ability to measure heart rate, respiratory rate, single-lead electrocardiography, and blood oxygen saturation.

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Adults over 18 years of age. * Undergoing anesthesia-assisted endoscopic procedures. * Able to give appropriate consent to the study or have an appropriate representative to do so. Exclusion Criteria: * Pregnancy. * Physical deformity, wound, or dressing preventing placement of a wearable device on the wrist. * Allergy to aluminum, nickel or acrylate.

Locations (1)

Mayo Clinic in Rochester

Rochester, Minnesota, United States