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NCT Number: NCT07310303

Simulation-Based Preoperative Education in Total Knee Arthroplasty

This randomized controlled trial aims to evaluate the effect of simulation-based preoperative education on surgical fear and kinesiophobia in patients undergoing total knee arthroplasty. Eligible patients are randomly assigned to either a simulation-based education group or a standard verbal education (control) group. Surgical fear, kinesiophobia, and postoperative pain are assessed using validated measurement tools. The findings of this study are expected to contribute to evidence-based nursing practices by informing the development of effective preoperative education strategies to improve postoperative recovery outcomes.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Acibadem Mehmet Ali Aydinlar University

Istanbul, 34752, Turkey (Türkiye)

About this study

Total knee arthroplasty is a major orthopedic surgical procedure that may lead to significant physical and psychological challenges for patients during the perioperative period. In addition to postoperative pain and functional limitations, patients frequently experience surgical fear and fear of movement (kinesiophobia), which may negatively affect early mobilization and recovery. Preoperative education is considered an essential nursing intervention to support patients in coping with these challenges; however, the optimal method for delivering such education remains an area of ongoing research.

Simulation-based education has increasingly been used in healthcare education to enhance understanding, reduce uncertainty, and improve preparedness by allowing individuals to actively engage with the anticipated care process. While its effectiveness has been well documented in student education, evidence regarding its use in preoperative patient education, particularly in orthopedic surgery, is limited.

This randomized controlled trial aims to examine the effect of simulation-based preoperative education on surgical fear and kinesiophobia in patients undergoing primary total knee arthroplasty. Eligible patients are randomly assigned to either an intervention group receiving simulation-based preoperative education or a control group receiving standard verbal preoperative education according to institutional routine practice. The educational intervention is delivered one day prior to surgery.

Data are collected using validated instruments, including the Surgical Fear Questionnaire, the Tampa Scale of Kinesiophobia, and the Visual Analog Scale for pain assessment. Surgical fear is assessed during the preoperative period, while kinesiophobia and postoperative pain are evaluated following surgery during the early mobilization phase.

The results of this study are expected to provide evidence to inform nursing-led preoperative education strategies and to support the development of patient-centered approaches aimed at improving psychological preparedness and postoperative recovery in individuals undergoing total knee arthroplasty.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 18 years and older
  • Scheduled for primary total knee arthroplasty
  • Able to communicate and cooperate
  • Able to speak and understand Turkish
  • No diagnosed major psychiatric disorder
  • No diagnosed neurological disorder
  • Willing to participate and able to provide written informed consent

Exclusion criteria

  • Revision total knee arthroplasty
  • Bilateral total knee arthroplasty
  • Total knee arthroplasty performed due to trauma
  • Presence of neurological, traumatic, or systemic conditions that may limit mobility
  • Development of postoperative surgical or prosthesis-related complications
  • Development of any condition preventing postoperative mobilization

Treatment and study plan

Simulation-Based Preoperative Education

Other

Simulation-based education provided preoperatively to prepare patients for postoperative mobilization and recovery.

Standard Verbal Preoperative Education

Other

Routine verbal preoperative education provided according to institutional standards.

Total knee arthroplasty

Procedure

All participants in both study arms undergo standard total knee arthroplasty performed according to institutional clinical protocols.

Primary outcomes

  1. Surgical Fear

    Time frame: Preoperative period (one day before surgery)

    Surgical fear will be assessed using the Surgical Fear Questionnaire, a validated self-report instrument measuring short-term and long-term fear related to surgery. Surgical fear will be assessed using the Surgical Fear Questionnaire, a validated self-report instrument measuring short-term and long-term fear related to surgery. Scores range from 0 to 80, with higher scores indicating greater levels of surgical fear.

Secondary outcomes

  1. Kinesiophobia

    Time frame: Postoperative period after recovery of cognitive function

    Kinesiophobia will be measured using the Tampa Scale of Kinesiophobia, a validated self-report scale assessing fear of movement and re-injury. Scores range from 17 to 68, with higher scores indicating greater levels of kinesiophobia.

  2. Postoperative Pain Intensity

    Time frame: Early postoperative period during first mobilization

    Postoperative pain intensity will be assessed using the Visual Analog Scale (VAS). Scores range from 0 to 10, with higher scores indicating greater pain intensity.

Sponsors and collaborators

Lead sponsor

Nermin Ocaktan

Other

Registry information

Official study title

The Effect of Simulation-Based Preoperative Education on Surgical Fear and Kinesiophobia in Patients Undergoing Total Knee Arthroplasty: A Randomized Controlled Trial

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 30, 2025
Registry last updated
May 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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