Augmented Reality Perioperative Training and Patient Satisfaction

NCT ID: NCT04727697

Last Updated: 2022-11-08

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

140 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-15

Study Completion Date

2022-10-04

Brief Summary

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

Detailed Description

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Conditions

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Anxiety State

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

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.

Group Type ACTIVE_COMPARATOR

Standard of Care preoperative teaching and handouts

Intervention Type OTHER

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.

Group Type EXPERIMENTAL

Augmented Reality

Intervention Type OTHER

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

Intervention Type OTHER

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.

Intervention Type OTHER

Standard of Care preoperative teaching and handouts

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

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Miami

OTHER

Sponsor Role lead

Responsible Party

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Lee Kaplan

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

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

Site Status

Countries

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United States

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.

Reference Type DERIVED
PMID: 37589975 (View on PubMed)

Other Identifiers

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20201439

Identifier Type: -

Identifier Source: org_study_id

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