Wearable Technology in Endoscopy

Mayo Clinic

Status: Completed

Conditions: Healthy

Treatments: Device: Consumer-facing wearable smart watch

Study type: Interventional

Funder types: Other

Identifiers

NCT05044104

21-007738

Details and patient eligibility

About

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

Full description

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.

Enrollment: 292 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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292 participants in 1 patient group

Wearable technology in endoscopic gastrointestinal procedures with sedation

Experimental group

Description:

Subjects undergoing a endoscopic gastrointestinal procedure with sedation as part of standard of care will wear a consumer-facing wearable smart watch for the duration of the procedure.

Treatment:

Device: Consumer-facing wearable smart watch