Clinical trial Recruiting at 1 site Observational Ages 6 to 17

Digitizing and automating diagnostic interviews for children and teens with mental health concerns

Official title: Digitizing and Automating the Diagnostic Psychiatric Assessment Process

Run by Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud · NCT07468214 · Data updated 2026-11-12

This project will test a Spanish digital interview (EPSI-C) to see if it helps diagnose children and teens aged 6–17 referred for mental health care.

Quick facts

Study typeObservational
Ages6 Years to 17 Years
SexAll
Enrollment35 (estimated)
SponsorFundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud
Academic / other
Locations1 site (Málaga, Málaga)
StatusRecruiting
StartedJanuary 9, 2026
Main results expectedOctober 1, 2026
Study endsFebruary 1, 2027
Registry record updatedMarch 12, 2026
Trial IDNCT07468214 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children aged 6–17 with a mental health referral from primary care and a stable caregiver able to report clinical history, without moderate-to-severe intellectual disability or global developmental disorder, are ideal candidates.

Probably not a fit

Children under state care without a stable caregiver, those with global developmental disorders or moderate-to-severe intellectual disability, or those with incomplete or unclear medical data may not receive benefit from this tool.

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

What this trial studies

This is a real-world, prospective, multicenter, single-arm observational effort within an international consortium to digitize and automate diagnostic evaluation in child and adolescent psychiatry using an explainable AI–based solution. The Spanish team is responsible for WP1, which covers translation, cross-cultural adaptation, and validation of the Electronic Semi-Structured Psychiatric Interview for Children and Adolescents (EPSI-C) based on DSM-5 criteria. WP4 will run a pilot feasibility validation across and within countries to test integration of the EPSI-C with new technologies and AI to support diagnostic workflows. The study recruits children aged 6–17 referred from primary care and compares EPSI-C outputs against clinical information gathered in routine care.

Why it matters

Potential benefit: If successful, this could make diagnostic interviews faster and more consistent, helping children get the right care sooner.

How similar studies have gone: The EPSI-C was developed in Sweden and similar digital semi-structured interview tools have shown promise for improving diagnostic consistency, but cross-cultural validation is still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion criteria:

\- Families and children aged 6 to 17 with a mental health referral from primary care.

Exclusion criteria:

* Minors under state care without stable attachment figures to report clinical history.
* Presence of global developmental disorder or moderate to severe intellectual disability.
* Incomplete, inaccurate, or unclear medical data.

Where it's running

  • Plaza del Hospital Civil s/n, Pabellón 4, 1ª Planta
    Málaga, Málaga, Spain
    Recruiting

Study contacts

  • Principal investigator: Marina Romero-González, Doctor — Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina y Salud
  • Study coordinator: Irene Lopez Armenteros, PhD student
  • Email: ireloar@gmail.com
  • Phone: +34687415627

Similar studies

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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.