The Effect of Video Education on Anesthesia Choice

March 8, 2026 updated by: Ali Genc, Tokat Gaziosmanpasa University

The Effect of Preoperative Artificial Intelligence-Based Video Education on Anxiety and Anesthesia Preference in Patients Scheduled for Arthroscopic Lower Extremity Surgery

This prospective single-group study aims to evaluate the effect of preoperative artificial intelligence-based video education on anxiety, anesthesia preference, satisfaction, and knowledge level in patients undergoing arthroscopic lower extremity surgery.

Study Overview

Status

Enrolling by invitation

Conditions

Detailed Description

Participants' demographic characteristics (age, gender, occupation, education level, income, marital status) will be recorded.

All patients will complete the Spielberger State Anxiety Inventory (STAI-I) before and after watching an AI-generated preoperative information video that explains anesthesia options and the perioperative process.

Their anesthesia preference, satisfaction, and knowledge level will also be assessed before and after the video.

The study aims to determine whether AI-based video education can reduce preoperative anxiety, alter anesthesia preference, and improve patient satisfaction and understanding.

Study Type

Observational

Enrollment (Estimated)

88

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey (Türkiye)
    • Tokat Province
      • Tokat Province, Tokat Province, Turkey (Türkiye), 60100
        • Tokat Gaziosmanpasa University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Adult patients aged 18 to 65 years scheduled for elective arthroscopic lower extremity surgery at Tokat Gaziosmanpaşa University Faculty of Medicine Hospital, Department of Anesthesiology and Reanimation.

Description

Inclusion Criteria:

  • Scheduled for elective arthroscopic lower extremity surgery
  • Able to understand the educational material
  • Voluntarily agrees to participate and provides written informed consent

Exclusion Criteria:

  • Mentally unable to provide valid responses
  • Communication barriers or severe visual impairment
  • Contraindication to regional or general anesthesia
  • Illiteracy or inability to understand Turkish

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
The effect of AI-based video education on preoperative anxiety and anesthesia preference
Patients will watch an artificial intelligence-based preoperative video explaining anesthesia options and perioperative care. The Spielberger State Anxiety Inventory, satisfaction scale, and knowledge questionnaire will be applied before and after the video education. The impact of artificial intelligence-based video training on anesthesia preference will be evaluated.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in anesthesia preference
Time Frame: Baseline (before the AI-assisted video information) and immediately after the AI-assisted video information, within the preoperative assessment period.
The impact of artificial intelligence-based video training on anesthesia preference will be evaluated.
Baseline (before the AI-assisted video information) and immediately after the AI-assisted video information, within the preoperative assessment period.
Change in Preoperative Anxiety Score (STAI-I)
Time Frame: Baseline (before the AI-assisted video information) and immediately after the AI-assisted video information, within the preoperative assessment period
To evaluate whether AI-based video education reduces preoperative anxiety. The State Anxiety Inventory (STAI-I) is a validated self-report instrument consisting of 20 items assessing situational anxiety. Scores range from 20 to 80, with higher scores indicating greater anxiety. A higher score reflects a worse outcome.
Baseline (before the AI-assisted video information) and immediately after the AI-assisted video information, within the preoperative assessment period

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Tokat Gaziosmanpasa University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 20, 2025

Primary Completion (Estimated)

May 1, 2026

Study Completion (Estimated)

June 1, 2026

Study Registration Dates

First Submitted

November 17, 2025

First Submitted That Met QC Criteria

November 20, 2025

First Posted (Actual)

November 24, 2025

Study Record Updates

Last Update Posted (Actual)

March 10, 2026

Last Update Submitted That Met QC Criteria

March 8, 2026

Last Verified

November 1, 2025

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 25-MOBAEK-127

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

The data used to support the findings of this study are available from the corresponding author upon reasonable request.

IPD Sharing Access Criteria

Researchers interested in accessing the data should contact the corresponding author via email with a brief description of their proposed use

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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