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ADRIS Driving Simulator for Adolescents With Attention Deficit and Hyperactivity Disorder

ADRIS Driving Simulator for Adolescents With Attention Deficit and Hyperactivity Disorder

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07478458
Acronym
ADRIS-ADHD
Enrollment
120
Registered
2026-03-17
Start date
2025-11-10
Completion date
2028-01-01
Last updated
2026-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ADHD - Attention Deficit Disorder With Hyperactivity

Keywords

ADHD, Driving simulator

Brief summary

This study aims to evaluate a new driving simulator, called ADRIS 2.1, developed for adolescents aged 13-18 years with Attention Deficit Hyperactivity Disorder (ADHD). ADHD is a common neurodevelopmental disorder that can affect attention, self-control, and decision-making. These challenges may impact daily activities, including driving. The ADRIS simulator allows participants to "drive" in a virtual environment while their performance is monitored. The system measures driving errors (such as not stopping at red lights), head and body movements, and heart rate, helping researchers understand how ADHD may affect driving-related behavior. Participants in the study will include both adolescents with ADHD and typically developing adolescents. All participants will complete standardized cognitive and behavioral assessments and take part in at least one driving simulation session. Adolescents with ADHD will return for follow-up visits and a subgroup will participate in a 6-week training program using the simulator. The main goal of the study is to measure differences in driving performance and attention between adolescents with and without ADHD. The study will also explore whether the simulator can detect improvements over time and in response to clinical treatment or simulator-based training. The results may help inform future clinical evaluations and support tools for adolescents with ADHD, with the potential to improve safety and quality of life.

Detailed description

INTRODUCTION Attention Deficit Hyperactivity Disorder (ADHD) is a common neurodevelopmental condition characterized by persistent symptoms of inattention, hyperactivity, and impulsivity. These impairments can significantly impact an adolescent's daily functioning, academic achievement, and social development. Among the various life skills affected by ADHD, driving represents a particularly complex and high-risk activity, requiring the integration of cognitive, attentional, and executive functions. Adolescents with ADHD are disproportionately involved in traffic violations and accidents compared to their neurotypical peers, largely due to reduced inhibitory control, poor hazard perception, and increased distractibility. Traditional clinical assessments often fail to capture how cognitive and behavioral deficits associated with ADHD manifest in ecologically valid tasks such as driving. Existing tools are limited in their ability to provide objective, task-based evaluations of attention and self-regulation under realistic conditions. Moreover, there is a scarcity of tailored assessment instruments for the adolescent ADHD population, especially those that can be integrated into clinical pathways for diagnosis, monitoring, and intervention. RATIONALE OF THE STUDY This study addresses the need for innovative tools to assess and monitor cognitive-behavioral functioning in adolescents with ADHD. We introduce ADRIS 2.1, a customizable driving simulation platform specifically designed for this population. ADRIS integrates real-time measurement of driving behavior, physiological response (heart rate), and body movements, offering a safe and standardized environment for testing attention, impulse control, and decision-making in dynamic scenarios. Unlike conventional evaluations, ADRIS allows for adaptive testing: the simulation parameters (e.g., scenario duration, obstacle type, voice prompts) can be modified to match the cognitive load and attentional profile of the user. This flexibility enables clinicians to replicate real-world challenges while collecting objective, quantifiable data related to attentional lapses, impulsive actions, and physiological stress responses. The study aims to validate ADRIS as a clinical support tool by comparing the driving performance of adolescents with and without ADHD, assessing the correlation between simulator outcomes and standardized neuropsychological tests, and analyzing changes in driving behavior following usual clinical interventions (pharmacological and non-pharmacological). In addition, the study explores whether repeated training with ADRIS may contribute to improvements in attention regulation and driving strategies. DEVICE DESCRIPTION ADRIS 2.1 is a driving simulator composed of the following components: * Steering wheel and pedals connected to a PlayStation console * 32" monitor displaying high-resolution driving environments * Integrated camera system for tracking head and torso movements * Heart rate monitor positioned on the left pectoral area The system is supported by software developed on the Unreal Engine platform, designed to: * Generate realistic urban and suburban driving scenarios * Provide interactive navigation with auditory guidance * Present neutral, congruent, and incongruent visual stimuli to test attentional control * Acquire and analyze metrics such as lane crossing, reaction time, speed variability, and physiological responses STUDY OBJECTIVES Primary Objective: Compare the number of traffic violations (e.g., ignored stop signs, red lights, speed limits, collisions) between adolescents with ADHD and neurotypical controls as an index of impulsivity and attentional regulation. Secondary Objectives: * Analyze body movement and heart rate data to assess physiological and behavioral differences during driving tasks * Correlate simulator performance with standardized neuropsychological test results * Monitor intra-individual changes over time (baseline vs. follow-up) to assess the impact of clinical treatments * Evaluate the effect of repeated ADRIS-based training on driving behavior and attentional control in a randomized subgroup PARTICIPANTS A total of 120 participants (60 ADHD, 60 controls) aged 13 to 18 years will be enrolled across two centers: IRCCS Istituto Giannina Gaslini (Genoa) and IRCCS Fondazione Stella Maris (Pisa). Recruitment will include both clinic-referred individuals and participants engaged via ADHD family associations and educational institutions. STUDY PROCEDURES T0 (All participants): ADHD group: full neuropsychological battery, standardized questionnaires (e.g., WISC/WAIS, NEPSY-II, CBCL, CONNERS 3), first ADRIS session (6 driving scenarios) Control group: short screening questionnaire, ADRIS simulator session (same protocol) T1 (ADHD only): At 3 months: repeat ADRIS session and neuropsychological assessments (excluding cognitive battery) T2 Sub-study (ADHD only): 30 ADHD participants will be randomized into two age- and sex-matched groups: Training group: 12 simulator training sessions over 6 weeks Control group: no training Both subgroups will undergo pre- and post-training ADRIS testing and neuropsychological evaluation (excluding cognitive battery) STIMULI AND TASK DESIGN During simulator sessions, participants will encounter: * Neutral stimuli: non-threatening static obstacles (e.g., trash bins) * Congruent stimuli: dynamic, context-appropriate obstacles (e.g., pedestrian crossing) * Incongruent stimuli: misleading cues followed by sudden hazards (e.g., decoy pedestrian followed by car) These scenarios test attentional capture, inhibition, and adaptive decision-making. Each session lasts \ 30 minutes. Statistical Analysis Sample size was calculated using G\*Power for independent-sample t-tests, assuming a medium effect size (d = 0.5), a power of 95%, and an alpha level of 0.05. This yielded a requirement of 54 participants per group. To account for an estimated 10% dropout rate, the total sample size was increased to 120 participants (60 per group). The primary outcome (number of traffic violations) will be analyzed using parametric or non-parametric tests, depending on the distribution and homogeneity of variance of the data. Secondary outcomes will be analyzed as follows: * Correlation analyses (Pearson or Spearman) to assess relationships between clinical and instrumental measures. * Repeated measures ANOVA or Friedman tests for within-subject comparisons over time. * Mixed-model ANOVA for analyzing training effects, with group as a between-subject factor and time as a within-subject factor. Both statistical significance (p-values) and clinical relevance will be evaluated to interpret the results meaningfully. ETHICAL CONSIDERATIONS The study will follow the Declaration of Helsinki and GCP standards. Ethics approval has been obtained from the National Pediatric Ethics Committee. Participants will provide informed consent/assent. Risks are minimal and limited to possible simulator-related discomfort (e.g., motion sickness). Mitigation protocols and trained staff will ensure participants' safety. POTENTIAL BENEFITS While no direct clinical benefits are guaranteed, participants may gain greater awareness of their attentional functioning. The study will contribute to developing novel clinical tools for ADHD assessment and training, potentially improving treatment personalization and long-term outcomes in adolescents.

Interventions

DEVICEADRIS-ADHD

30 ADHD participants will be divided into two subgroups: 15 will undergo an intensive training program with the ADRIS simulator (12 sessions, twice a week for 6 weeks), and they will be evaluated pre- and post-training through driving simulator test sessions and neuropsychological testing excluding cognitive evaluation. A comparator arm of 15 patients will partecipate only in evaluation sessions with no training.

Sponsors

Istituto Giannina Gaslini
Lead SponsorOTHER
IRCCS Fondazione Stella Maris
CollaboratorOTHER
University of Genova
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

In the first phase of the study, 60 subjects with ADHD will be assessed using neuropsychological tests, while 60 control subjects without ADHD will complete a brief questionnaire to evaluate attentional and executive functioning. Both groups will also be assessed through the performance of tasks using the ADRIS driving simulator. In the second phase, subjects with ADHD will undergo a follow-up assessment using neuropsychological tests (excluding cognitive evaluation) and tasks on the ADRIS driving simulator, in order to investigate any cognitive-behavioral changes following the therapy prescribed as per standard of care. In the third phase, 30 subjects with ADHD will be divided into two groups of 15 subjects each. One group will complete neuropsychological tests (excluding cognitive evaluation) and driving simulator tasks before and after a training cycle of ADRIS, while the other group will undergo the same assessments without the training.

Eligibility

Sex/Gender
ALL
Age
13 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

for ADHD subjects: * Age range 13-18 years (up to the age of nineteen) * Diagnosis of ADHD (hyperactive, inattentive and combined subtype) * Consent to participate in the study by the participant or, in the case of a minor, by their parent(s)/guardian(s). Inclusion Criteria for Control Group subjects: * Age- and sex-matched neurotypical adolescents * No diagnosis of ADHD or other neurodevelopmental disorders * Informed consent obtained from the participant if of legal age or from the legal guardian and assent from the minor

Exclusion criteria

* Visual deficits not corrected/correctable with the normal use of lenses. * Motor deficits clinically detected and/or previously diagnosed and that could compromise the use of the simulator (e.g. neurological diseases, psychiatric diseases, etc.). * Categorical diagnoses according to DSM-5 criteria such as Psychosis, Mood Disorders, Autism Spectrum Disorders, Intellectual Disabilities, Borderline Intellectual Functioning, Anxiety Disorders. * Patients with other conditions that could affect driving ability. * Denial / withddrawal of consent to the protocol

Design outcomes

Primary

MeasureTime frameDescription
Attention assessment in adolescents with / without ADHD using ADRIS driving simulator[Baseline - T0] Day 0Difference in total number of driving infractions in adolescents with / without ADHD, assessed using ADRIS driving simulator. Number of infractions (N) are calculated as the sum of: * ignored stop signs (N) * ignored red lights (N) * collisions (N) * wrong way driving (N) * speed limits ignored (N) * ignored safety distance (N). These measures are directly provided by the simulator). Unit of measure: count (N)

Secondary

MeasureTime frameDescription
Heart rate differences in driving subjects (adolescents with / without ADHD)[Baseline - T0] Day 0Heart rate (HR) during driving task, measured using a wearable chest strap with heart rate sensor. Unit of measure: beats per minute (bpm) This measure is directly provided by the simulator
Heart rate variability differences in driving subjects (adolescents with / without ADHD)[Baseline - T0] Day 0Heart rate variability (HRV) during driving task, measured using a wearable chest strap with heart rate sensor. Calculated as mean and standard deviation of R-R intervals. Unit of measure: milliseconds (ms) This measure is directly provided by the simulator
Trunk movements differences in driving subjects (adolescents with/without ADHD)[Baseline - T0] Day 0Trunk movements on frontal and sagittal planes, extracted from stereo camera recordings. Unit of measure: degrees (°) This measure is directly provided by the simulator
Head direction differences in driving subjects (adolescents with/without ADHD)[Baseline - T0] Day 0Head direction (heading) during driving task, extracted from stereo camera recordings. Unit of measure: degrees (°) This measure is directly provided by the simulator
Cognitive assessment with Wechsler Scale in ADHD patients[Baseline - T0] Day 0Cognitive assessment will be performed depending on subjects' age with * Wechsler Intelligence Scale for Children - 4th Edition (WISC IV) \[Total standard score, Perceptual Reasoning Index score, Block Design score, Picture Concepts score, Matrix Reasoning score, Working Memory Index score, Digit Span score, Letter-Number Sequencing score, Processing Speed Index score, Coding score, Symbol Search score, Cancellation score\] * Wechsler Adult Intelligence Scale - 4th Edition (WAIS IV) \[Total standard score, Perceptual Reasoning Index score, Block Design score, Visual Puzzles score, Matrix Reasoning score, Working Memory Index score, Digit Span score, Arithmetic score, Processing Speed Index score, Coding score, Symbol Search score, Cancellation score\]
Behavior, adaptive skills and emotional-behavioral difficulties assessment in ADHD patients, as reported by their parents or primary caregivers.[Baseline - T0] Day 0 [T1] Month 3 [T2] 6 weeks after [T0] or [T1]Assessment will be performed through administration of the following questionnaire: Child Behavior CheckList (CBCL) Parent Form \[Anxious/Depressed percentile score, Withdrawn/Depressed percentile score, Somatic Complaints percentile score, Social Problems percentile score, Thought Problems percentile score, Attention Problems percentile score, Rule-Breaking Behavior percentile score, Aggressive Behavior percentile score, Internalizing Problems percentile score, Externalizing Problems percentile score, Other Problems percentile score, Total Problems percentile score, Depressive Problems percentile score, Anxiety Problems percentile score, Somatic Problems percentile score, Attention Deficit/Hyperactivity percentile score, Oppositional Defiant Problems percentile score, Conduct Problems percentile score, Sluggish Cognitive Tempo percentile score, Obsessive-Compulsive Problems percentile score, Stress Problems percentile score\]
Self reported behavior, adaptive skills and emotional-behavioral difficulties assessment in ADHD patients[Baseline - T0] Day 0, [T1] Month 3, [T2] 6 weeks after [T0] or [T1]Assessment will be performed through administration of the following questionnaire: Youth Self Report 11-18 Form \[Anxious/Depressed percentile score, Withdrawn/Depressed percentile score, Somatic -Complaints percentile score, Social Problems percentile score, Thought Problems percentile score, Attention Problems percentile score, Rule-Breaking Behavior percentile score, Aggressive Behavior percentile score, Internalizing Problems percentile score, Externalizing Problems percentile score, Total Problems percentile score, Affective Problems percentile score, Anxiety Problems percentile score, Somatic Problems percentile score, Attention Deficit/Hyperactivity percentile score, Oppositional Defiant Problems percentile score, Conduct Problems percentile score, Stress Problems percentile score, Positive Qualities percentile score, Obsessive-Compulsive Problems percentile score\]
Attention, behavior, and emotional regulation assessment in ADHD patients[Baseline - T0] Day 0 [T1] Month 3 [T2] 6 weeks after [T0] or [T1]Assessment will be performed through administration of the following questionnaires: * Conners-3 Parent Form \[ADHD Index score, Inattention percentile score, Hyperactivity/Impulsivity percentile score, Learning Problems percentile score, Executive Functioning percentile score, Defiance/Aggression percentile score, Peer Relations percentile score, Global Index T score\] * Conners-3 Self Report Form \[ADHD Index score, Inattention percentile score, Hyperactivity/Impulsivity percentile score, Learning Problems percentile score, Executive Functioning percentile score, Defiance/Aggression percentile score, Peer Relations percentile score, Global Index T score\]
Visual-Motor Integration assessment in ADHD patients[Baseline - T0] Day 0 [T1] Month 3 [T2] 6 weeks after [T0] or [T1]Assessment will be performed through administration of the following: Developmental Test of Visual-Motor Integration \[Total standard score, Total scaled score, Visual standard score, Visual scaled score, Motor standard score, Motor scaled score\]
Sustained and selective attention assessment in ADHD patients[Baseline - T0] Day 0 [T1] Month 3 [T2] 6 weeks after [T0] or [T1]Assessment will be performed through administration of the following: \- NEPSY II (A Developmental Neuropsychological Assessment - Second Edition) \[Auditory Attention total percentile score, Response Set total percentile score, Naming Attention Time scaled score, Naming Total Errors percentile score, Naming Combination scaled score, Inhibition Attention Time scaled score, Inhibition Total Errors percentile score, Inhibition Combination scaled score, Switching Attention Time scaled score, Switching Total Errors percentile score, Switching Combination scaled score\]
Inhibitory control and cognitive interference assessment in ADHD patients[Baseline - T0] Day 0 [T1] Month 3 [T2] 6 weeks after [T0] or [T1]Assessment will be performed through administration of the following: Stroop Test \[Color Naming score, Incongruent Naming score, Corrected score, Equivalent score\]

Countries

Italy

Contacts

CONTACTLino Nobili, MD PhD
linonobili@gaslini.org+3901056262381
PRINCIPAL_INVESTIGATORLino Nobili, MD PhD

IRCCS Istituto Giannina Gaslini

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026