Actively Recruiting
Behavioral Parent Training With and Without AI Support for Children With Disruptive Behaviors
Led by Fundació Sant Joan de Déu · Updated on 2026-03-13
40
Participants Needed
1
Research Sites
47 weeks
Total Duration
On this page
Sponsors
F
Fundació Sant Joan de Déu
Lead Sponsor
P
Parente AI
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Behavioral Parent Training With and Without AI Support for Children With Disruptive Behaviors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- 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.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hospital Sant Joan de Déu
Barcelona, Barcelona, Spain, 08950
Actively Recruiting
Research Team
P
Pablo Vidal-Ribas Belil, PhD
CONTACT
E
Eduardo L Bunge, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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