Clinical trial Recruiting at 1 site Observational Ages 5 to 12

Personalized therapeutic stories for children after kidney transplant.

Official title: Generating Personalized Stories With Artificial Intelligence for Pediatric Kidney Recipients

Run by Paris Translational Research Center for Organ Transplantation · NCT07532382 · Data updated 2026-11-12

We will test whether clinician-supervised AI can create age-appropriate, personalized therapeutic stories for children aged 5–12 who have received a kidney transplant and their families.

More Kidney Transplant trials

Quick facts

Study typeObservational
Ages5 Years to 12 Years
SexAll
Enrollment100 (estimated)
SponsorParis Translational Research Center for Organ Transplantation
Academic / other
Locations1 site (Paris, Île-de-France Region)
StatusRecruiting
StartedMarch 1, 2026
Main results expectedDecember 1, 2026
Study endsDecember 1, 2026
Registry record updatedApril 15, 2026
Trial IDNCT07532382 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 5–12 who have received a kidney transplant, are clinically stable, fluent in French or English, and whose parents/guardians can provide consent and commit to study visits are ideal candidates.

Probably not a fit

Children with severe cognitive impairment, an unstable clinical course (such as active rejection or hospitalization), families unable to participate in interviews, or non–French/English speakers are unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project develops an AI-assisted workflow that uses large language models to generate age-adapted, personalized therapeutic stories for pediatric kidney transplant recipients and their families. Clinicians supervise story generation and tailor content via interviews and iterative feedback to ensure medical accuracy and emotional safety. Participants aged 5–12 who are clinically stable and fluent in French or English will receive AI-generated stories and be followed for acceptability, usability, and psychosocial outcomes. The study is conducted at Necker Hospital in Paris and focuses on feasibility and refinement rather than testing clinical efficacy.

Why it matters

Potential benefit: If successful, the approach could provide a scalable, clinician-approved way to help children process transplant experiences, reduce anxiety, and support family communication.

How similar studies have gone: Narrative and therapeutic storytelling have shown benefit in pediatric psychosocial care, but the use of clinician-supervised large language models to generate personalized stories for transplant patients is novel and not yet proven.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Necker hospital
    Paris, Île-de-France Region, France
    Recruiting

Study contacts

  • Principal investigator: Marc Raynaud, PhD — Paris Institute for Transplantation and Organ Regeneration
  • Study coordinator: Marc Raynaud, PhD
  • Email: mrayna06@gmail.com
  • Phone: +33613493009

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.