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The Effect of Virtual Tour Training Before Orthopedic Surgery

I

Istanbul University - Cerrahpasa

Status

Completed

Conditions

Satisfaction
Anxiety

Treatments

Other: No Interventions
Other: Virtual Tour

Study type

Interventional

Funder types

Other

Identifiers

NCT06936540
IUC-SN-SB-01

Details and patient eligibility

About

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.

Full 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.

Enrollment

70 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

70 participants in 2 patient groups

Intervention group
Other group
Description:
The intervention group will be trained by the researcher with a virtual tour material about surgical environments via a tablet computer.
Treatment:
Other: Virtual Tour
Control group
Other group
Description:
The control group will not receive any intervention other than verbal training in the routine of the organization.
Treatment:
Other: No Interventions

Trial contacts and locations

1

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Central trial contact

Nuray Akyüz, Assoc. Prof.; Seda Baydemir, PhD-candidate

Data sourced from clinicaltrials.gov

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