Clinical trial Recruiting at 1 site Interventional Ages 5 to 12

Behavioral parent training with optional AI support for children with disruptive behaviors

Official title: A Pilot Randomized Controlled Trial of Behavioral Parent Training (BPT) With or Without AI Support in Children With Disruptive Behaviors

Run by Fundació Sant Joan de Déu · NCT07469215 · Data updated 2026-11-12

This trial will test whether adding a 24/7 AI assistant to online group behavioral parent training helps parents manage children aged 5–12 with disruptive behaviors.

Quick facts

Study typeInterventional
Ages5 Years to 12 Years
SexAll
Enrollment40 (estimated)
SponsorFundació Sant Joan de Déu
Academic / other
Locations1 site (Barcelona, Barcelona)
StatusRecruiting
StartedApril 2026
Main results expectedMarch 2027
Study endsMarch 2027
Registry record updatedMarch 13, 2026
Trial IDNCT07469215 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Primary caregivers (Spanish- or Catalan-speaking) of children aged 5–12 with disruptive behaviors who have reliable internet access, stable concurrent treatments, and are willing to attend eight weekly online group sessions.

Probably not a fit

Families where the child has a primary autism diagnosis, severe mood disorder, psychosis, intellectual disability (IQ < 70), active self-harm, or who are already receiving concurrent psychological treatment are excluded and 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 randomized controlled trial compares standard online Behavioral Parent Training (BPT) with BPT plus continuous access to ParenteAI, a 24/7 virtual assistant that offers personalized guidance between sessions. Parents attend eight weekly online group sessions and are randomized to receive the app or not, with outcomes measured at baseline and follow-ups over six months. The primary focus is feasibility and acceptability (utility, satisfaction, therapeutic alliance, attendance, dropout), and secondary outcomes include child disruptive behaviors and irritability and parent depression, anxiety, and stress. Participants are Spanish- or Catalan-speaking primary caregivers of children aged 5–12 with disruptive behavior problems who have regular internet access.

Why it matters

Potential benefit: If successful, the AI app could provide immediate, personalized support between sessions, improving access to care and reducing children's disruptive behaviors and parental stress.

How similar studies have gone: Behavioral Parent Training is a well-established effective treatment for disruptive behaviors, and while digital adjuncts have shown promise, continuous AI virtual assistants are relatively novel and less tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Being a primary caregiver with a child aged 5 to 12 years exhibiting disruptive behaviors (e.g., symptoms of ODD, CD, IED, ADHD, and/or unspecified behavioral problems).
* Having access to an electronic device and regular internet access.
* Stable concomitant intervention including medications throughout the study.
* Speak Spanish or Catalan language.
* Signed informed consent by parents or legal guardians of the child.

Exclusion Criteria:

* Having ASD as primary diagnosis.
* Psychosis, self-harming behaviors, severe mood disorder.
* Known Intelligent quotient \< 70
* Caregivers and/or children receiving any concurrent psychological treatment.
* No signing the informant consent.

Where it's running

  • Hospital Sant Joan de Déu
    Barcelona, Barcelona, Spain
    Recruiting

Study contacts

  • Principal investigator: Pablo Vidal-Ribas Belil, PhD — Fundació de Recerca Sant Joan de Déu
  • Study coordinator: Pablo Vidal-Ribas Belil, PhD
  • Email: pablo.vidalribas@sjd.es
  • Phone: +34644890465

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.