Evaluating a Digital Cognitive Training Intervention in Adults With ADHD
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Digital Cognitive Training, Digital Non-cognitive Training Intervention.
- Кому может быть актуально
- Состояния в реестре: ADHD. Базовые параметры: 18 лет — 65 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Список центров уточняется — проверьте первичный протокол.
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Не всё понятно в терминах? Прочитайте наш гид для пациентов →
Официальное название
Evaluating the Feasibility and Tolerability of a Digital Cognitive Training Intervention in Adults With ADHD: A Randomized, Placebo-controlled Trial
Обзор
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
Вмешательства
- Другое Digital Cognitive Training
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. - Другое Digital Non-cognitive Training Intervention
This is a gamified computer platform lacking cognitive training components.
Первичные конечные точки
- Number of participants who prematurely withdraw from the study protocol [Срок оценки: From enrollment to the end of treatment at 11 weeks]
- The feasibility of digital cognitive training on ADHD symptoms in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
Вторичные конечные точки (6)
- The effect of digital cognitive training on ADHD symptoms in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
- The effects of digital cognitive training on problematic internet use in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
- The effects of digital cognitive training on visual processing and working memory in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
- The effects of digital cognitive training on cognitive flexibility in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
- The effects of digital cognitive training on working memory in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
- The effects of digital cognitive training on verbal short-term and working memory in adults diagnosed with ADHD of moderate-severe severity [Срок оценки: From enrollment to the end of treatment at 11 weeks]
Критерии участия
Критерии включения
- 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.
Критерии исключения
- 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.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Простое слепое
- Основная цель
- Лечение
Центры проведения
Список центров уточняется — проверьте первичный протокол.
Идентификаторы
NCT: NCT07050225 · DCOG_ADHD