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Artificial Intelligence-Supported Visual Guide for Preschool Children Undergoing Medical Procedures

Effect of an Artificial Intelligence-Supported Visual Guide on Procedural Anxiety, Pain, and Post-Procedural Behavioral Changes in Preschool Children Undergoing Common Medical Procedures: A Multicenter Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07704112
Acronym
AIVIP
Enrollment
110
Registered
2026-07-15
Start date
2026-04-14
Completion date
2026-05-30
Last updated
2026-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavioral Changes, Procedural Anxiety, Procedural Pain

Keywords

Artificial Intelligence, Preschool Children, Medical Procedures, Procedural Preparation, Procedural Anxiety, Procedural Pain, PHBQ-AS, mYPAS, FLACC, Pediatric Nursing, Child-Centered Care, Family Health Centers, Randomized Controlled Trial, Non-pharmacological Intervention, Digital Health, Google Gemini, CapCut

Brief summary

Children frequently experience anxiety, pain, and negative behavioral changes during common medical procedures such as venous blood sampling, vaccination, injection, and peripheral intravenous catheter insertion. Providing developmentally appropriate procedural preparation before these procedures may improve children's experiences and reduce procedure-related distress. This multicenter randomized controlled trial evaluates the effectiveness of an artificial intelligence (AI)-supported visual guide developed to prepare preschool children aged 3-6 years for common medical procedures. The intervention consists of standardized 1-3-minute procedure-specific educational videos created using Google Gemini 2.5 Pro (Google DeepMind) and finalized using CapCut. The videos incorporate researcher-developed educational scripts, AI-generated illustrations, and AI-generated voice narration to provide child-friendly, visually engaging, and developmentally appropriate procedural preparation. A total of 110 children are randomly assigned to either an intervention group receiving the AI-supported visual guide before the procedure or a control group receiving routine care. The primary outcome is procedural anxiety assessed using the Modified Yale Preoperative Anxiety Scale (mYPAS). Secondary outcomes include procedural pain measured using the Face, Legs, Activity, Cry, and Consolability (FLACC) Pain Scale and post-procedural behavioral changes measured using the Post Hospitalization Behavior Questionnaire for Ambulatory Surgery (PHBQ-AS).

Detailed description

Medical procedures such as venous blood sampling, vaccination, injection, and peripheral intravenous catheter insertion are among the most common sources of anxiety and distress in preschool children. Inadequate preparation before these procedures may increase procedural anxiety, pain perception, and negative behavioral responses, potentially affecting future healthcare experiences and treatment adherence. Developmentally appropriate, child-centered educational interventions are recommended to improve children's understanding of medical procedures and reduce procedure-related distress. Recent advances in artificial intelligence (AI), particularly multimodal generative AI systems, have created new opportunities for developing personalized, engaging, and age-appropriate educational materials. However, evidence regarding the effectiveness of AI-generated visual preparation tools in reducing procedural anxiety, pain, and post-procedural behavioral changes in preschool children remains limited. This multicenter randomized controlled trial evaluates the effectiveness of an AI-supported visual guide developed specifically for preschool children aged 3-6 years undergoing common medical procedures in family health centers. The intervention consists of standardized procedure-specific educational videos created using Google Gemini 2.5 Pro (Google DeepMind) and finalized using CapCut. Educational scripts are developed by the research team based on evidence related to trauma-informed care, child- and family-centered care, procedural preparation, and non-pharmacological interventions. AI-generated illustrations and voice narration are combined with researcher-developed content to produce four standardized educational videos for venous blood sampling, vaccination, injection, and peripheral intravenous catheter insertion. Each video lasts approximately 1-3 minutes and introduces the healthcare environment, healthcare professionals, medical equipment, procedural steps, and positive reinforcement following completion of the procedure. Children are randomly assigned to either an intervention group receiving the AI-supported visual guide approximately 15 minutes before the medical procedure or a control group receiving routine care. Procedural anxiety is assessed using the Modified Yale Preoperative Anxiety Scale (mYPAS) before, during, and immediately after the procedure. Procedural pain is assessed using the Face, Legs, Activity, Cry, and Consolability (FLACC) Pain Scale, while post-procedural behavioral changes are evaluated 15 days after the procedure using the Post Hospitalization Behavior Questionnaire for Ambulatory Surgery (PHBQ-AS). The primary objective of the study is to determine whether AI-supported visual preparation reduces procedural anxiety in preschool children. Secondary objectives are to evaluate its effects on procedural pain and post-procedural behavioral changes. This study is designed to evaluate the effectiveness of AI-assisted, child-centered visual education as a standardized, scalable, and non-pharmacological intervention for procedural preparation in preschool children undergoing common medical procedures.

Interventions

BEHAVIORALAI-Supported Visual Guide

A standardized 1-3-minute, AI-supported, procedure-specific educational video developed using Google Gemini 2.5 Pro and finalized using CapCut. The videos included researcher-developed educational scripts, AI-generated illustrations, and AI-generated voice narration to prepare preschool children for venous blood sampling, vaccination, injection, and peripheral intravenous catheter insertion. The videos were shown approximately 15 minutes before the procedure.

Sponsors

Istanbul Bilgi University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants were randomly assigned in a 1:1 ratio to either an intervention group receiving an AI-supported procedure-specific visual guide before the medical procedure or a control group receiving routine care. Participants remained in their assigned group throughout the study, and outcomes were compared between the two parallel groups.

Eligibility

Sex/Gender
ALL
Age
3 Years to 6 Years
Healthy volunteers
Yes

Inclusion criteria

* Children aged 3-6 years. * Scheduled to undergo venous blood sampling, vaccination, injection, or peripheral intravenous catheter insertion at participating family health centers. * Able to understand Turkish. * Parent or legal guardian provided written informed consent. * Child provided verbal assent when developmentally appropriate.

Exclusion criteria

* Diagnosed neurological, developmental, or psychiatric disorders that could interfere with behavioral assessment. * Visual or hearing impairment preventing participation in the intervention. * Administration of sedative or analgesic medication before the procedure. * Previous participation in this study. * Parent or child unwilling to participate.

Design outcomes

Primary

MeasureTime frameDescription
Procedural AnxietyImmediately before, during, and immediately after the medical procedure.Procedural anxiety measured using the Modified Yale Preoperative Anxiety Scale (mYPAS). The mYPAS total score ranges from 23.3 to 100, with higher scores indicating greater procedural anxiety.

Secondary

MeasureTime frameDescription
Procedural PainImmediately after the medical procedure.Procedural pain assessed using the Face, Legs, Activity, Cry, and Consolability (FLACC) Pain Scale. Total scores range from 0 to 10, with higher scores indicating greater procedural pain.
Post-Procedural Behavioral Changes15 days after the medical procedure.Post-procedural behavioral changes assessed using the Post Hospitalization Behavior Questionnaire for Ambulatory Surgery (PHBQ-AS). Total scores range from 11 to 55, with higher scores indicating more negative post-procedural behavioral changes.

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATOREbru Temizsoy, PhD,RN

İstanbul Bilgi University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 16, 2026