Behavioral Parent Training With and Without AI Support for Children With Disruptive Behaviors
NCT07469215 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2026-03-13
Summary
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
- Behavior Problem of Childhood and Adolescence
- Parent Management Training
- Artificial Intelligence (AI)
- Disruptive Behaviours
- Irritability
- Attention Deficit Disorder With Hyperactivity (ADHD)
Interventions
- BEHAVIORAL
-
Behavioral Parent Training (BPT)
Eight (8) weekly online sessions of BPT
- COMBINATION_PRODUCT
-
Behavioral Parent Training (BPT) + Support of AI app
Eight (8) weekly online sessions of BPT supported by AI app, with access 24/7 from baseline to 6 month follow up after last group session.
Sponsors & Collaborators
-
Parente AI
collaborator UNKNOWN -
Fundació Sant Joan de Déu
lead OTHER
Principal Investigators
-
Pablo Vidal-Ribas Belil, PhD · Fundació de Recerca Sant Joan de Déu
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 5 Years
- Max Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-04-30
- Primary Completion
- 2027-03-31
- Completion
- 2027-03-31
Countries
- Spain
Study Locations
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