Brief Smartphone Treatment Study
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: Mindfulness ecological momentary intervention, Self-monitoring placebo.
- Кому может быть актуально
- Состояния в реестре: Generalized Anxiety Disorder. Базовые параметры: от 18 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
- США
- 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
Brief Smartphone Treatment Study for Anxiety and Depression
Обзор
Little is known about whether and how brief mindfulness therapies yield clinically beneficial effects. This gap exists despite the rapid growth of smartphone mindfulness applications and presence of mental health treatment gap. Specifically, no prior brief, smartphone mindfulness ecological momentary intervention (MEMI) has targeted generalized anxiety disorder (GAD). Moreover, although theories propose that mindfulness intervention can boost attentional control (AC), executive functioning (EF), perspective-taking, and social cognition skills they have largely gone untested. Thus, this randomized controlled trial (RCT) aims to address these gaps by assessing the efficacy of a 14-day smartphone mindfulness EMI (vs. placebo). Participants with GAD will be randomly assigned to either MEMI or self-monitoring placebo (SMP). Those in treatment will exercise multiple core mindfulness strategies (open monitoring, acceptance, attending to small moments, slowed rhythmic diaphragmatic breathing). Also, those in MEMI will be reminded before bedtime that mindfulness is a lifelong practice. Comparatively, participants assigned to SMP will only be prompted to practice self-monitoring. They will notice their thoughts, rate any distress associated with them, and will not be taught any mindfulness strategies. All prompts will occur 5 times a day, for 14 consecutive days. They will complete self-reports and neuropsychological assessments at pre-, post-, and 1-month follow-up. Multilevel modeling analyses will determine if treatment (vs. self-monitoring placebo (SMP)) produces substantially larger reductions in trait worry and negative perseverative cognitions as well as steeper increases in AC and EF (inhibition, set-shifting, working memory updating). In addition, the investigators hypothesized that MEMI (vs. SMP) would lead to greater increases in performance-based and self-reported trait mindfulness, empathy, and perspective taking. Findings will advance understanding of the efficacy of unguided, technology-assisted, brief mindfulness in a clinical sample.
Вмешательства
- Устройство Mindfulness ecological momentary intervention
Access to a smartphone-delivered mindfulness ecological momentary intervention with the Personal Analytics Companion (PACO) app that regularly prompts participants to practice various mindfulness skills at 5 preset times each day. - Устройство Self-monitoring placebo
Access to a smartphone-delivered self-monitoring placebo with the PACO app that regularly prompts participants to practice self-monitoring at 5 preset times each day.
Первичные конечные точки
- Change from Baseline Generalized Anxiety Disorder Symptoms at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Generalized Anxiety Disorder Symptoms at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
- Change from Baseline Perseverative Cognitions at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Perseverative Cognitions at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
Вторичные конечные точки (12)
- Change from Baseline Depression Symptom Severity at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Depression Symptom Severity at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
- Change from Baseline Attentional Control at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Attentional Control at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
- Change from Baseline Working Memory at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Working Memory at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
- Change from Baseline Set-Shifting at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Set-Shifting at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
- Change from Baseline Inhibitory Control at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Inhibitory Control at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
- Change from Baseline Verbal Fluency at 14-Day Post-Treatment [Срок оценки: Baseline to 14-Day Post-Treatment]
- Change from Baseline Verbal Fluency at 6-Week Post-Randomization [Срок оценки: Baseline to 6-Week Post-Randomization]
Критерии участия
Критерии включения
- Presence of Generalized Anxiety Disorder based on the Generalized Anxiety Disorder Questionnaire-IV self-report and Mini International Neuropsychiatric Interview
- Current student at the Pennsylvania State University or a community-dwelling adult who expressed interest to participate through the PSU StudyFinder portal
- Expressed interest to seek treatment
- Currently not receiving treatment from a mental health professional
- Able to provide consent
- Proficient in English
Критерии исключения
- Below age 18
- Failure to meet any of above inclusion criteria
- Participant currently undergoing
- Presence of suicidality, mania, psychosis, or substance use disorders
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
США · 1 центр
- The Pennsylvania State University — University Park
Публикации
- Zainal NH, Newman MG. Who engages? Machine learning insights into digital mindfulness-based intervention for generalized anxiety disorder. J Affect Disord. 2026 Apr 15;399:120963. doi: 10.1016/j.jad.2025.120963. Epub 2025 Dec 19. PMID 41422949
- Zainal NH, Newman MG. Examining the Effects of a Brief, Fully Self-Guided Mindfulness Ecological Momentary Intervention on Empathy and Theory-of-Mind for Generalized Anxiety Disorder: Randomized Controlled Trial. JMIR Ment Health. 2024 May 24;11:e54412. doi: 10.2196/54412. PMID 38787613
Идентификаторы
NCT: NCT04846777 · STUDY00010664