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Evaluating a Digital Cognitive Training Intervention in Adults With ADHD

Evaluating the Feasibility and Tolerability of a Digital Cognitive Training Intervention in Adults With ADHD: A Randomized, Placebo-controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07050225
Enrollment
52
Registered
2025-07-03
Start date
2025-08-31
Completion date
2026-02-28
Last updated
2025-07-22

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

Conditions

ADHD

Keywords

ADHD, Attention Deficit Hyperactivity Disorder, Problematic Internet Use, PIU, Cognitive Training Intervention, Executive Functioning, Adult ADHD, ADHD Symptoms, Digital Health, Adjunct Therapy, Hyperactivity, Attention

Brief summary

The goal of this clinical trial is to evaluate whether a digital cognitive training program can reduce symptoms of ADHD, improve executive functioning, and decrease problematic internet use in adults aged 18-65 with a diagnosis of moderate to severe ADHD. The main questions it aims to answer are: Can digital cognitive training improve executive function, and ADHD symptoms in adults with ADHD? Does digital cognitive training reduce problematic internet use in this population? Researchers will compare the digital cognitive training intervention group to a non-cognitive training digital platform to see if the training leads to greater improvements in cognitive and behavioral outcomes. Participants will: Complete an 11-week digital cognitive training program (3, 1-hour sessions/week) or placebo intervention (3, 1-hour sessions/week) Attend baseline, midpoint, and post-intervention assessments Participate in weekly check-ins to monitor engagement and tolerability

Interventions

This digital cognitive training program uses gamified tasks in order to enhance cognitive skills in an engaging manner using machine learning AI algorithms to target the intervention to individual cognitive skill deficits. It consists of personalized gamified cognitive tasks that target individual cognitive deficits associated with ADHD including attention, impulsivity, working memory, and cognitive flexibility.

OTHERDigital Non-cognitive Training Intervention

This is a gamified computer platform lacking cognitive training components.

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Participants must provide informed consent and agree to comply with study protocols for the duration of the study. * Participants must be fluent in speaking and reading English and able to complete rating scales and assessments. * Participants must be adults aged 18-65 years. * Participants must have a clinical diagnosis of ADHD based on DSM-5 Criteria, as confirmed by the Mini Neuropsychiatric interview. * Participants being treated with pharmacotherapy must be stable and on a consistent dose for at least 6 weeks prior to study entry. * Participants must have access to a computer capable of running the cognitive training platform. * Participants must be comfortable operating a computer and be able to log on to the platform without assistance.

Exclusion criteria

* Exclude individuals who meet DSM-5 criteria for psychiatric conditions such as borderline personality disorder, schizophrenia, severe depression, or other psychotic disorders as well as neurological conditions such as epilepsy, dementia, and amnesia, that may interfere with cognitive training. * Exclude participants with active substance use disorders. * Exclude participants receiving behavioral therapy or undergoing similar cognitive training programs for ADHD and/or PIU. * Exclude individuals with severe visual, auditory, or motor impairments that affect the ability to perform the digital cognitive training intervention. * Exclude participants who are uncomfortable using applications or required technology. * Exclude participants who have changed their treatment regimen in the last 6 weeks. * Exclude participants who are not fluent in English.

Design outcomes

Primary

MeasureTime frameDescription
The feasibility of digital cognitive training on ADHD symptoms in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksFeasibility will be evaluated based on the number of people who contact the study team, percent of people who contact who are eligible, and percent of eligible participants who enroll. Percent of participants lost to follow-up will be a key determinant of feasibility, as well as number of completers.
Number of participants who prematurely withdraw from the study protocolFrom enrollment to the end of treatment at 11 weeksTolerability of the digital cognitive training intervention will be assessed by calculating the number of participants who discontinue participation before completing the full 11-week study protocol. Premature withdrawal will be defined as any participant who discontinues the intervention and/or does not complete post-treatment assessments.

Secondary

MeasureTime frameDescription
The effects of digital cognitive training on problematic internet use in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksChanges in the severity of problematic internet use will be evaluated via changes in Compulsive Internet Use Scale (CIUS) scores.
The effects of digital cognitive training on visual processing and working memory in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksPerformance on Trails A and B task will be evaluated.
The effect of digital cognitive training on ADHD symptoms in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksADHD symptom severity will be measured via the Barkley Adult ADHD Rating Scale (BAARS-IV). The minimum score on the Barkley ADHD Rating Scale is 0, and the maximum score is 54. The scale consists of 18 items, each rated on a scale of 0 to 3, where 0 indicates the absence of the symptom and 3 indicates a high level of severity.
The effects of digital cognitive training on verbal short-term and working memory in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksPerformance on the Digit Span Test will be evaluated.
The effects of digital cognitive training on cognitive flexibility in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksPerformance on Berg's Card Sorting Task will be evaluated.
The effects of digital cognitive training on working memory in adults diagnosed with ADHD of moderate-severe severityFrom enrollment to the end of treatment at 11 weeksPerformance on N-back Task will be evaluated.

Other

MeasureTime frameDescription
Changes on symptoms of anxietyFrom enrollment to the end of treatment at 11 weeksThe Generalized Anxiety Disorder 7-item (GAD-7), a 7-item questionnaire will be used to screen for the severity of symptoms of anxiety. The Generalized Anxiety Disorder 7-item (GAD-7) scale has a minimum score of 0 and a maximum score of 21. The scale uses a 4-point Likert scale for each of its 7 items, ranging from 0 (Not at all) to 3 (Nearly every day). Higher scores indicate more severe anxiety symptoms.
Changes on symptoms of depressionFrom enrollment to the end of treatment at 11 weeksThe Patient Health Questionnaire (PHQ)-9, the major depressive disorder (MDD) module of the full PHQ will be used to measure the severity of depressive symptoms. The PHQ-9 is a widely used tool for assessing depression severity. The minimum possible score on the PHQ-9 is 0, and the maximum is 27. Each of the 9 questions is scored from 0 to 3, with higher scores indicating more severe symptoms.
Changes in quality of lifeFrom enrollment to the end of treatment at 11 weeksWorld Health Organization Quality of Life Brief Version (WHOQOL-BREF) will be used to assess impairment and quality of life. The WHOQOL-BREF (World Health Organization Quality of Life Brief Version) is scored on a 1-5 scale for each of the 26 items. These scores are then transformed to a 0-100 scale. The minimum possible score for each domain is 0, representing the worst possible quality of life, and the maximum is 100, representing the best possible quality of life.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026