Augmented Reality Perioperative Training and Patient Satisfaction

Not Applicable

Completed

• Conditions: Anxiety State
• Interventions: Other: Augmented Reality; Other: Standard of Care preoperative teaching and handouts

• Registration Number: NCT04727697
• Lead Sponsor: University of Miami

Brief Summary

The purpose of this study is to learn more about how augmented reality systems can influence perioperative experience and patient satisfaction.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2021-01-22
• Study First Submitted QC: 2021-01-22
• Study First Posted: 2021-01-27
• Study Start: 2021-05-15
• Primary Completion: 2022-09-22
• Study Completion: 2022-10-04
• Status Verified: 2022-11
• Last Update Submitted: 2022-11-07
• Last Update Posted: 2022-11-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 140

Inclusion Criteria

• All patients 18 years old or greater
• Patients who have a scheduled ambulatory procedure with University of Miami Orthopaedic providers.

Exclusion Criteria

• Any patient not scheduled for procedures
• Minors
• Cognitively incapacitated
• Prisoners.
• Have any condition that, in the opinion of the investigator, would compromise the well-being of the patient or the study or prevent the patient from meeting or performing study requirements.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Augmented Reality perioperative experiences group	Augmented Reality	The participants in this group will receive the preoperative teaching and handouts as is the current standard of care in addition to receiving the augmented reality (AR) perioperative experience.
Augmented Reality perioperative experiences group	Standard of Care preoperative teaching and handouts	The participants in this group will receive the preoperative teaching and handouts as is the current standard of care in addition to receiving the augmented reality (AR) perioperative experience.
Standard of Care, preoperative teaching group	Standard of Care preoperative teaching and handouts	The participants in this group will receive the preoperative teaching and handouts as is the current standard of care.

Primary Outcome Measures

Name	Time	Method
Change in Anxiety as measured by the state-trait anxiety inventory (STAI)	Baseline, up to 14 days	STAI has scores ranging from 20 to 80 with higher scores corresponding to greater levels of anxiety.

Secondary Outcome Measures

Name	Time	Method
Change in comfort level as measured by perioperative comfort questionnaire	Baseline, up to 14 days	Perioperative comfort questionnaire ranges from 1-5 with higher scores indicating greater levels of comfort.

Trial Locations

Locations (1)

University of Miami; 🇺🇸 Miami, Florida, United States