Immersive Technology in the Pediatric Perioperative Phase of Care for Mask Inductions Integration

Overview

About this study

The purpose of this study is to utilize a projector based software (Sevo and Desi, invincikids.org) and a screen connected to patient transport bed to engage with pediatric patients in the perioperative environments and assess implementation effectiveness in the perioperative care flow and satisfaction using the technology from patients, staff, and parents. 

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:

  • Pediatric patients aged 4-18 years, listed for surgery on NT3 in the pediatric perioperative area. Patients and their parents must provide verbal assent and consent.

Exclusion Criteria:

  • Patients with a history of severe motion sickness, seizure disorder, or unwillingness to participate will not be included. In addition, if they are too anxious to comply with an orientation to the immersive technology being offered, they will not be included.

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

Eligibility last updated 11/1723. 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

Rochester, Minn.

Mayo Clinic principal investigator

Kathryn Handlogten, M.D.

Open for enrollment

Contact information:

Kathryn Handlogten M.D.

(507) 255-6219

Handlogten.Kathryn@mayo.edu

More information

Publications

Publications are currently not available