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Augmented Reality Perioperative Training and Patient Satisfaction

Patient Reported Outcomes, Satisfaction, and Understanding Following Orthopaedic Ambulatory Procedures Using Augmented/Virtual Reality as an Education Tool

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04727697
Enrollment
140
Registered
2021-01-27
Start date
2021-05-15
Completion date
2022-10-04
Last updated
2022-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety State

Brief summary

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

Interventions

OTHERAugmented Reality

Patients will receive the preoperative AR experience during their immediately preoperative office visit. The duration of the exposure is approximately 15 minutes.

OTHERStandard of Care preoperative teaching and handouts

At preoperative appointments, patients receive verbal teaching and written handouts about day of surgery instructions and expectations.

Sponsors

University of Miami
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

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

Secondary

MeasureTime frameDescription
Change in comfort level as measured by perioperative comfort questionnaireBaseline, up to 14 daysPerioperative comfort questionnaire ranges from 1-5 with higher scores indicating greater levels of comfort.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026