The Effect of Virtual Tour Training Before Orthopedic Surgery

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

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-04-12

Study Completion Date

2025-10-12

Brief Summary

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The purpose of the study is to determine the effect of training on surgical environments provided with virtual tour before orthopedic surgical ıntervention on patients' anxiety and satisfaction level.

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Detailed Description

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Although preoperative anxiety is accepted as a normal patient response, severe anxiety can lead to a number of negative physiological, emotional and cognitive consequences for patients and ultimately to prolonged hospitalization. If anxiety is not managed effectively in the preoperative period, recovery time is prolonged and the risk of anesthesia and surgery-related complications increases. Moreover, it can lead to respiratory distress and cardiac problems. It causes life threats by increasing the risk of bleeding with deterioration in hemodynamic parameters and negatively affects surgical outcomes and patient satisfaction. For all these reasons, this study was designed to contribute to the management of anxiety, which is seen as a problem that needs to be addressed in surgical nursing.

Conditions

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Anxiety Satisfaction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The study was planned as an open-label, randomized, controlled, parallel group interventional study. Participants will be randomly assigned to either the intervention group or the control group. The intervention group will be trained by the researcher with a virtual tour material about surgical environments via a tablet computer. The control group will not receive any intervention other than verbal training in the routine of the organization.

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Intervention group

The intervention group will be trained by the researcher with a virtual tour material about surgical environments via a tablet computer.

Group Type OTHER

Virtual Tour

Intervention Type OTHER

The intervention group will be trained by the researcher with a virtual tour material about surgical environments via a tablet computer.

Control group

The control group will not receive any intervention other than verbal training in the routine of the organization.

Group Type OTHER

No Interventions

Intervention Type OTHER

The control group will not receive any intervention other than verbal training in the routine of the organization.

Interventions

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Virtual Tour

The intervention group will be trained by the researcher with a virtual tour material about surgical environments via a tablet computer.

Intervention Type OTHER

No Interventions

The control group will not receive any intervention other than verbal training in the routine of the organization.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Between the ages of 18-65
* Being literate
* No comprehension and perception problems
* No hearing and vision problems
* Not being under psychiatric treatment
* No surgical experience
* To undergo elective orthopedic surgery in the operating room
* Acceptance to participate in the research