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Набор скоро начнётся NCT07553364

Auditory Stimulation for Insomnia and Depression

Без фазы С лечением Depression - Major Depressive Disorder Insomnia

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: Alpha phase-locked auditory stimulation, Sham Stimulation.
Кому может быть актуально
Состояния в реестре: Depression - Major Depressive Disorder, Insomnia. Базовые параметры: 20 лет — 50 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 →
Официальное название

Feasibility of Using Alpha Phase-Locked Auditory Stimulation for Insomnia Symptoms in People With Depression

Обзор

The goal of this clinical trial is to determine if alpha phase-locked auditory stimulation can improve sleep in people with insomnia and depression. The main goals of the pilot study are the following: Determine whether alpha phase-locked auditory stimulation (active stimulation) improves objective and subjective sleep in individuals with insomnia and depression. The study team hypothesizes that active auditory stimulation will reduce objective and subjective sleep onset latency (SL) and wake after sleep onset (WASO) compared to a sham stimulation. Participants will: * Wear Elemind Neuromod headband nightly for 4 weeks (1 week baseline, 1 week active/sham stimulation, 1 week washout, and 1 week opposite condition - active/sham stimulation) * Wear actigraphy watch for duration of the study * Complete questionnaires regarding their sleep, mood, and satisfaction with the device

Подробное описание

The purpose of this pilot study is to determine if non-invasive alpha-phase locked auditory stimulation delivered before sleep can improve objective and subjective sleep outcomes in individuals with depression and insomnia. Moreover, the study team will determine if this protocol design is feasible and acceptable to this population to inform the design of a larger scale clinical trial in this population.

Insomnia is highly prevalent among individuals with major depressive disorder (MDD) and is a strong risk factor for onset and recurrence. Effective treatment of insomnia has been shown to accelerate antidepressant response and reduce suicidal ideation. Insomnia is associated with increased cortical arousal during sleep, reflected by elevated alpha, beta, and theta EEG activity. Although cognitive behavioral therapy for insomnia (CBT-I) and pharmacologic treatments can improve sleep and depression, CBT-I is time-intensive and often inaccessible, while medications pose risks of side effects, dependence, and patient reluctance. Scalable, home-based neuromodulation during sleep represents a promising alternative.

Elemind has developed a closed-loop, audio-driven neurostimulation device that reduces sleep latency by modulating alpha oscillations during pre-sleep quiet wakefulness. The device uses a wearable headband to track sleep stages and deliver precisely timed auditory stimulation to reduce alpha activity and facilitate sleep onset. The auditory stimulation can be applied both at the beginning of the night, and following nighttime awakenings to help reduce sleep onset latency and wake after sleep onset.

After screening and enrolling in the study, participants will wear the headband to sleep nightly for up to 4 weeks, including one week of baseline, one week of either active or sham stimulation, 1 week of washout, and 1 final week of the opposite stimulation condition. Participants will also wear an actigraphy watch and keep a sleep diary throughout the duration of the study. Finally, participants will complete several questionnaires regarding their sleep, mood, and satisfaction with the device throughout the study.

Вмешательства

  • Устройство Alpha phase-locked auditory stimulation
    Using the ENMod device, participants will receive alpha phase-locked auditory stimulation delivered as pink noise pulses through a bone conduction driver placed near the middle of the forehead. To mask the sound of the stimulation, natural rain sounds will be played alongside the pink noise.
  • Устройство Sham Stimulation
    Using the ENMod device, participants will receive sham stimulation, which is presented as natural rain sounds alone, through a bone conduction driver placed near the middle of the forehead.

Первичные конечные точки

  • Sleep Onset Latency - Measurement 1 [Срок оценки: from baseline to week 2]
  • Wake after sleep onset - Measurement 1 [Срок оценки: from baseline to week 2]
  • Sleep Onset Latency - Measurement 2 [Срок оценки: from baseline to week 4]
  • Wake after sleep onset - Measurement 2 [Срок оценки: from baseline to week 4]
Вторичные конечные точки (7)
  • Insomnia Severity Index [Срок оценки: Baseline, Week 2, Week 4]
  • Epworth Sleepiness Scale (ESS) [Срок оценки: Baseline, Week 2, Week 4]
  • Patient Health Questionnaire (PHQ-9) [Срок оценки: Baseline, Week 2, Week 4]
  • Beck's Depression Inventory (BDI) [Срок оценки: Baseline, Week 2, Week 4]
  • Satisfaction Survey [Срок оценки: Week 2, Week 4]
  • Subjective Sleep Onset Latency [Срок оценки: Baseline, Week 2, Week 4]
  • Subjective wake after sleep onset [Срок оценки: Baseline, Week 2, Week 4]

Критерии участия

Критерии включения

  • Ability to complete overnight EEG study including placement of EEG leads
  • Ability to read and understand English
  • Presence of Insomnia
  • Moderate Depression
  • Home internet and smartphone (Android or Apple) device access

Критерии исключения

  • Presence of severe, untreated sleep apnea
  • Presence of restless leg syndrome
  • Significant neurological disease (e.g. Parkinson's disease, epilepsy)
  • Diagnosed with schizophrenia, bipolar disorder, substance use disorder, or presence of current suicidal ideation
  • Has active implanted device ( e.g. intracranial device, cochlear implant)
  • Currently deaf or experiencing hearing loss or using hearing aids
  • Currently taking medications that could alter EEG
  • Currently pregnant

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Перекрёстный дизайн
Маскирование
Двойное слепое
Основная цель
Лечение

Центры проведения

США · 1 центр
  • Wake Forest University Health Sciences — Winston-Salem

Публикации

  • Bressler S, Neely R, Yost RM, Wang D, Read HL. A wearable EEG system for closed-loop neuromodulation of sleep-related oscillations. J Neural Eng. 2023 Oct 5;20(5). doi: 10.1088/1741-2552/acfb3b. PMID 37726002
  • Peterson MJ, Benca RM. Sleep in mood disorders. Psychiatr Clin North Am. 2006 Dec;29(4):1009-32; abstract ix. doi: 10.1016/j.psc.2006.09.003. PMID 17118279
  • Bressler S, Neely R, Yost RM, Wang D. Author Correction: A randomized controlled trial of alpha phase-locked auditory stimulation to treat symptoms of sleep onset insomnia. Sci Rep. 2024 Sep 19;14(1):21867. doi: 10.1038/s41598-024-72802-4. No abstract available. PMID 39300282

Идентификаторы

NCT: NCT07553364 · IRB00145704

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗