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Augmented Reality Perioperative Training and Patient Satisfaction

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University of Miami

Status

Completed

Conditions

Anxiety State

Treatments

Other: Augmented Reality
Other: Standard of Care preoperative teaching and handouts

Study type

Interventional

Funder types

Other

Identifiers

NCT04727697
20201439

Details and patient eligibility

About

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

Enrollment

140 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

140 participants in 2 patient groups

Standard of Care, preoperative teaching group
Active Comparator group
Description:
The participants in this group will receive the preoperative teaching and handouts as is the current standard of care.
Treatment:
Other: Standard of Care preoperative teaching and handouts
Augmented Reality perioperative experiences group
Experimental group
Description:
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.
Treatment:
Other: Augmented Reality
Other: Standard of Care preoperative teaching and handouts

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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