Ireland
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Starting soon Not applicable

Evaluation of the LUSHA Digital Application for Children With ADHD - Feasibility Study

NCT07204873 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-10
Last updated
2025-10-02

Condition(s) studied

Attention Deficit Disorder With or Without Hyperactivity (ADHD)Children

Investigational drug(s) / intervention(s)

LUSHA digital app

LUSHA digital app: Children with Attention Deficit Disorder with or without Hyperactivity (ADHD) and their parents will be asked to use LUSHA app during 3 months.

Study summary

Attention Deficit Disorder with or without Hyperactivity (ADHD) is a neurodevelopmental disorder characterized by a triad of symptoms combining inattention, hyperactivity, and/or impulsivity. It causes developmental and functional disturbances (cognitive, behavioral, and emotional) that have a detrimental impact on the child's family, school, and/or social life. Treatment requires psychoeducation for the child and their parents, individual treatment for the child, and finally family treatment, particularly through specific parenting skills training programs (such as the Barkley program, 1997). It is sometimes necessary to combine this with medication (psychostimulants).

This care pathway can be complex to implement in practice, due to lack of regional actors (CMPPs, medical-psychological-educational centers) and a decrease in the number of child psychiatrists in hospital services.

Recently, digital applications enabling the digitization of the psychotherapeutic approach have been developed to complement and reinforce the care provided to these children, offering an immediately available non-pharmacological alternative.

LUSHA is a digital application (digital game) developed in collaboration with healthcare professionals. It aims to motivate the children to change their behavior and help parents to interact with them.

The goal of this observational study is to evaluate the adoption of LUSHA app by children with Attention deficit disorder with or without Hyperactivity (ADHD) and their parents :

* The primary objective of this study is to assess adherence/use of a digital application among children with ADHD and their parents over a period of 90 days
* The secondary objectives are to assess the clinical impact of the LUSHA digital application using validated questionnaires (i.e quality of life, behavioural, family functioning).

Participating children and their parents will be asked to use the LUSHA digital application during 3 months and to answer online surveys.

Eligibility

Sex
ALL
Min age
7 Years
Max age
12 Years
Healthy volunteers
No
Inclusion Criteria: * Children aged 7-12 years * Already diagnosed with ADHD * Consulting in a participating center * No indication of treatment changes (no treatment or medication stabilized for 2 months) * Family with a smartphone compatible with downloading the app * Non-opposition of both parents and the child (if possible) Exclusion Criteria: * Parent under guardianship or deprived of liberty

Primary outcome measure(s)

  • To evaluate the use of the LUSHA app among children and their parents at 3 months. — 90 days
    Use is defined as a cumulative usage of more than 30 minutes per week on average within 3 months (90 days) of app installation.

Trial sites (2)

FacilityCityRegionStatus
University Hospital, Grenoble Grenoble France
University Hospital, Montpellier Montpellier France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07204873 on ClinicalTrials.gov ↗ ← All trials in France