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Clinical Trials in France / NCT07532382
Recruiting Observational

Personalized Stories for Pediatric Kidney Recipients

NCT07532382 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2026-03-01
Last updated
2026-04-15

Condition(s) studied

Kidney Transplant

Investigational drug(s) / intervention(s)

AI-generated storyAI generated story

AI-generated story: A story generated by artificial intelligence is created and personalized for pediatric kidney recipient

AI generated story: This is a minimal-risk observational study. Families complete a questionnaire and receive an AI-generated, clinically supervised personalized story. During the pilot phase, there is no direct child-AI interaction. All stories are reviewed by the clinical lead before delivery.

Study summary

Pediatric kidney transplant recipients often face major psychosocial challenges that are difficult to address with existing tools. This study evaluates whether clinically supervised AI can generate personalized, age-adapted therapeutic stories for these children and their families.

Eligibility

Sex
ALL
Min age
5 Years
Max age
12 Years
Healthy volunteers
No
Inclusion Criteria: * Age 5-12 years inclusive at enrolment. * Recipient of a kidney transplant. * Clinically stable at enrolment (no active rejection, acute infection, or current hospitalization for a graft-related complication). * Fluency in French or English. * Written informed consent from parent(s)/legal guardian(s); child assent when age-appropriate. Exclusion Criteria: * Severe cognitive impairment precluding engagement with narrative content. * Mental state not allowing participation. * Family unwilling or unable to commit to the study timeline and interview requirements.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Necker hospital Paris Île-de-France Region Recruiting

More Paris Translational Research Center for Organ Transplantation trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07532382 on ClinicalTrials.gov ↗ ← All trials in France