Recruiting

XAI-COMMHuman-Centered Communication on AI-Supported Imaging for Reduced Preoperative Anxiety and Improved Perceived Control

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

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.

What is being tested

Human-Centered Explainable AI Communication

+ Standard Preoperative Information

BehavioralOther
Who is being recruted

From 18 to 65 Years
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: February 2026
See protocol details

Summary

Principal SponsorAgri Ibrahim Cecen University
Study ContactVolkan GOKMEN, DoctorateMore contacts
Last updated: February 12, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitlePerioperative Human-Centered Communication on AI-Supported Real-Time Imaging and Its Effects on Preoperative Anxiety and Perceived Control: A Randomized Controlled Trial
Principal SponsorAgri Ibrahim Cecen University
Study ContactVolkan GOKMEN, DoctorateMore contacts
Last updated: February 12, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

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

60 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

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.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants in this arm will receive standard preoperative information plus a structured, human-centered, non-technical explanation about AI-supported real-time imaging systems, focusing on their role, limitations, and relevance to patient safety.

Group II

Active Comparator
Participants in this arm will receive standard preoperative information routinely provided by the institution, without additional information related to AI-supported real-time imaging systems.

Study 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

Recruiting

Ağrı Training and Research Hospital

Ağrı, Turkey (Türkiye)Open Ağrı Training and Research Hospital in Google Maps
Recruiting
One Study Center
XAI-COMM | Human-Centered Communication on AI-Supported Imaging for Reduced Preoperative Anxiety and Improved Perceived Control | PatLynk