Augmented Reality Perioperative Training and Patient Satisfaction
NCT ID: NCT04727697
Last Updated: 2022-11-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
140 participants
INTERVENTIONAL
2021-05-15
2022-10-04
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Standard of Care, preoperative teaching group
The participants in this group will receive the preoperative teaching and handouts as is the current standard of care.
Standard of Care preoperative teaching and handouts
At preoperative appointments, patients receive verbal teaching and written handouts about day of surgery instructions and expectations.
Augmented Reality perioperative experiences group
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
Patients will receive the preoperative AR experience during their immediately preoperative office visit. The duration of the exposure is approximately 15 minutes.
Standard of Care preoperative teaching and handouts
At preoperative appointments, patients receive verbal teaching and written handouts about day of surgery instructions and expectations.
Interventions
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Augmented Reality
Patients will receive the preoperative AR experience during their immediately preoperative office visit. The duration of the exposure is approximately 15 minutes.
Standard of Care preoperative teaching and handouts
At preoperative appointments, patients receive verbal teaching and written handouts about day of surgery instructions and expectations.
Eligibility Criteria
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Inclusion Criteria
* Patients who have a scheduled ambulatory procedure with University of Miami Orthopaedic providers.
Exclusion Criteria
* 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.
18 Years
ALL
No
Sponsors
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University of Miami
OTHER
Responsible Party
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Lee Kaplan
Professor
Principal Investigators
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Lee Kaplan, MD
Role: PRINCIPAL_INVESTIGATOR
University of Miami
Locations
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University of Miami
Miami, Florida, United States
Countries
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References
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Rizzo MG Jr, Costello JP 2nd, Luxenburg D, Cohen JL, Alberti N, Kaplan LD. Augmented Reality for Perioperative Anxiety in Patients Undergoing Surgery: A Randomized Clinical Trial. JAMA Netw Open. 2023 Aug 1;6(8):e2329310. doi: 10.1001/jamanetworkopen.2023.29310.
Other Identifiers
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20201439
Identifier Type: -
Identifier Source: org_study_id
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