XAI-COMMHuman-Centered Communication on AI-Supported Imaging for Reduced Preoperative Anxiety and Improved Perceived Control
This study aims to reduce your preoperative anxiety by using AI-supported imaging communication, with the primary outcome being the change in your anxiety level as measured by the Amsterdam Preoperative Anxiety and Information Scale (APAIS) before and after the intervention.
Human-Centered Explainable AI Communication
+ Standard Preoperative Information
Prevention Study
Summary
Study start date: February 5, 2026
Actual date on which the first participant was enrolled.This study focuses on how patients feel and respond to the use of AI-supported real-time imaging systems in their care, particularly before surgery. It's common for patients to experience anxiety before an operation, and this study aims to understand if a clear, patient-friendly explanation about these technologies can help reduce this anxiety. The study is important as it doesn't just look at the technical side of AI in healthcare, but also considers the patient's psychological response. This could lead to better ways of communicating with patients about AI, improving their overall experience and satisfaction. Adults scheduled for elective surgery participate in this study. They are divided into two groups: one receives the usual pre-surgery information, while the other gets this standard information plus a brief, face-to-face explanation about AI-supported imaging systems. This explanation uses simple, non-technical language and covers the general purpose of these systems, their role in clinical practice, and their relation to patient safety. The study then measures changes in anxiety levels using the Amsterdam Preoperative Anxiety and Information Scale (APAIS). This scale is used before and after the information session, and the results are compared between the two groups.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.60 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: * Adults aged 18 to 65 years. * Scheduled for elective surgical procedures. * Able to communicate in Turkish. * At least primary school literacy. * Able and willing to provide written informed consent. Exclusion Criteria: * Emergency surgical procedures. * Known diagnosis of psychiatric disorders. * Current use of anxiolytic or antidepressant medications. * Cognitive impairment or communication barriers that may interfere with study participation.
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Ağrı Training and Research Hospital
Ağrı, Turkey (Türkiye)Open Ağrı Training and Research Hospital in Google Maps