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The Effect of Virtual Tour Training Before Orthopedic Surgery

The Effect of Training on Surgical Environments Provided With Virtual Tour Before Orthopedic Surgical Intervention on Patients' Anxiety and Satisfaction Level

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06936540
Enrollment
70
Registered
2025-04-20
Start date
2025-04-12
Completion date
2025-10-12
Last updated
2025-11-18

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

Conditions

Anxiety, Satisfaction

Keywords

Anxiety, Satisfaction, Virtual Reality, Orthopedic Surgical Procedures

Brief summary

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.

Detailed description

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.

Interventions

OTHERVirtual Tour

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

OTHERNo Interventions

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

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

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.

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Exclusion criteria

* To undergo emergency orthopedic surgery * Wishing to leave at any stage of the study

Design outcomes

Primary

MeasureTime frameDescription
State-Trait Anxiety Inventory (STAI): Pre-test and post-test differences of anxiety levelsFrom immediately before preoperative training to immediately after preoperative training (on the day before surgery).The State-Trait Anxiety Inventory (STAI) is accepted as the the gold standard to determine the level of anxiety. The validity and reliability of the STAI in Turkey was conducted by Oner and Le Compte. The STAI can be administered to individuals over the age of 14 and there is no time limit for answering. It includes two separate scales of twenty items each (ie, the State Anxiety Scale (STAI-S) and the Trait Anxiety Scale (STAI-T). STAI-S and STAI-T scores are calculated separately. The total score obtained from the scales varies between 20 and 80, and a high score indicates a high level of anxiety.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS) for Satisfaction: Pre-test and post-test differences of satisfaction levelsFrom immediately before preoperative training to immediately after preoperative training (on the day before surgery).The satisfaction form, created by the researcher using the Visual Analog Scale (VAS), includes a scale for patients to rate their satisfaction. Scoring is between 0 and 10 points (0 to 10 inclusive). A high score indicates a high level of satisfaction.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026