Behavioral Parent Training With and Without AI Support for Children With Disruptive Behaviors

Recruiting now · Not applicable

Conditions studied: Behavior Problem of Childhood and Adolescence, Parent Management Training, Artificial Intelligence (AI), Disruptive Behaviours, Irritability, Attention Deficit Disorder With Hyperactivity (ADHD)

In brief

The goal of this clinical trial is to learn if adding an artificial intelligence (AI) application called to standard Behavioral Parent Training (BPT) helps families with children who have disruptive behavior problems. It will also help researchers understand if the app is easy to use and helpful for parents. The main question it aims to answer is: \- Is it feasible and acceptable for parents to use the AI app alongside their therapy sessions? The secondary questions it aims to answer are: * Does the app help reduce children's disruptive behaviors and irritability more than therapy alone? * Does using the app help lower stress, anxiety, and depression levels for the parents? Researchers will compare: 1. Standard BPT: Parents receive 8 weekly group training sessions (online). 2. BPT plus ParenteAI: Parents receive the same 8 weekly sessions plus 24/7 access to an AI virtual assistant for personalized support. Participants will: * Attend 8 weekly group training sessions. * Complete surveys about their child's behavior and their own well-being at baseline, after group training sessions 4 and 8, and 3 and 6 months after finalizing the group training. * If in the experimental group, use the ParenteAI app to get real-time coaching and support for managing their child's behavior at home. * Provide feedback on their experience and satisfaction with the program.

Key facts

Study ID: NCT07469215
Run by: Fundació Sant Joan de Déu
People needed: 40
Starts: 2026-04-01
Expected to finish: 2027-03-01
Last updated by the study team: 2026-03-13

Who can join

Age: 5 and older, up to 12. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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.

You may not qualify if…

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 is running

Hospital Sant Joan de Déu — Barcelona, Barcelona, Spain (enrolling)

Full record on ClinicalTrials.gov

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