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Transcranial Direct Current Stimulation for Long COVID Brain Fog and Fatigue (NEUROSTIM-LC)

19 июля 2026 г. обновлено: David Morales Álamo, University of Las Palmas de Gran Canaria

The Impact of Transcranial Direct Current Stimulation on Quality of Life, Brain Fog, and Fatigue in Patients With Long COVID: Study Protocol of the NEUROSTIM-LC Study

Long COVID can cause persistent symptoms such as fatigue, cognitive difficulties commonly described as brain fog, reduced exercise tolerance, and impaired quality of life. Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that may help modulate brain activity in regions involved in cognition, fatigue, and executive function.

The NEUROSTIM-LC study will evaluate the feasibility and potential effects of repeated tDCS sessions in adults with long COVID presenting fatigue and/or brain fog. Participants will receive 30 sessions of tDCS applied over the left dorsolateral prefrontal cortex. Assessments will be performed before and after the intervention to evaluate changes in quality of life, fatigue, cognitive function, brain metabolism, physical performance, autonomic function, sleep quality, psychological symptoms, respiratory function, and blood biomarkers.

Обзор исследования

Статус

Еще не набирают

Условия

Вмешательство/лечение

Подробное описание

The NEUROSTIM-LC study is a prospective, single-arm, interventional before-and-after study designed to evaluate the feasibility, tolerability, and preliminary effects of transcranial direct current stimulation (tDCS) in patients with long COVID. The study will recruit adults aged 18 to 70 years diagnosed with long COVID according to World Health Organization criteria and presenting persistent fatigue and/or cognitive impairment commonly described as brain fog.

Participants will receive 30 sessions of tDCS delivered over consecutive weeks in a controlled clinical setting. Stimulation will be applied over the left dorsolateral prefrontal cortex, with the anode positioned at F3 according to the international 10-20 EEG system and the cathode over the contralateral supraorbital region. Each session will be delivered at 2 mA for 20 minutes. Sessions will be performed on weekdays under the supervision of trained healthcare professionals, and adherence, tolerability, and adverse effects will be monitored throughout the intervention period.

Assessments will be conducted at baseline and after completion of the intervention. Clinical outcomes will include health-related quality of life, fatigue, cognitive performance, sleep quality, anxiety and depression symptoms, and perceived symptom evolution. Neurobiological and physiological outcomes will include brain metabolism assessed by PET-CT, autonomic nervous system activity assessed by heart rate variability, exercise capacity assessed using the Ekblom-Bak submaximal cycle ergometer test, upper-limb muscle strength assessed by handgrip dynamometry, lower-limb neuromuscular performance assessed by countermovement jump testing, respiratory function, oxygen saturation, and routine blood biomarkers. Blood samples may also be stored for future analysis of inflammatory and oxidative stress markers.

The study aims to provide preliminary information on whether repeated tDCS may be associated with measurable improvements in fatigue, brain fog, quality of life, and physiological function in patients with long COVID. The findings will help inform the design of future controlled trials evaluating non-invasive neuromodulation strategies for persistent neurological and fatigue-related symptoms after COVID-19.

Тип исследования

Интервенционный

Регистрация (Оцененный)

20

Фаза

  • Непригодный

Контакты и местонахождение

В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.

Контакты исследования

  • Имя: Juan Francisco Vigueras, MD
  • Номер телефона: +34 606 63 86 98
  • Электронная почта: juanfraviguerasperez@yahoo.es

Учебное резервное копирование контактов

  • Имя: David Morales Álamo, PhD
  • Номер телефона: +34 623 062 814
  • Электронная почта: david.moralesalamo@ulpgc.es

Критерии участия

Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.

Критерии приемлемости

Возраст, подходящий для обучения

  • Взрослый
  • Пожилой взрослый

Принимает здоровых добровольцев

Нет

Описание

Inclusion Criteria:

  • Adults aged between 18 and 70 years.
  • Diagnosis of long COVID according to World Health Organization criteria, defined as symptoms persisting for at least three months after acute SARS-CoV-2 infection and lasting for a minimum of two months without an alternative explanation.
  • Presence of persistent fatigue and/or cognitive impairment, commonly described as brain fog, attributed to long COVID and confirmed at screening.
  • Stable clinical condition allowing participation in the intervention and assessment procedures.
  • Ability to understand the study procedures and provide written informed consent.

Exclusion Criteria:

  • Contraindications to transcranial direct current stimulation, including the presence of implanted electronic devices such as pacemakers or neurostimulators, intracranial metallic implants, or history of epilepsy or seizures.
  • History of neurological disorders that may affect cognitive function, including stroke, Parkinson's disease, or neurodegenerative disorders.
  • Pre-existing conditions associated with chronic fatigue or cognitive impairment prior to SARS-CoV-2 infection, such as fibromyalgia, chronic fatigue syndrome, or multiple sclerosis.
  • Severe psychiatric disorders, including psychosis or severe depression.
  • Substance abuse, including alcohol or drugs.
  • Current oncological treatment with chemotherapy or radiotherapy.
  • Pregnancy.
  • Any medical condition that, in the opinion of the investigators, may interfere with participation or with the interpretation of the results.

Учебный план

В этом разделе представлена ​​подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.

Как устроено исследование?

Детали дизайна

  • Основная цель: Уход
  • Распределение: Н/Д
  • Интервенционная модель: Одногрупповое задание
  • Маскировка: Нет (открытая этикетка)

Оружие и интервенции

Группа участников / Армия
Вмешательство/лечение
Экспериментальный: tDCS Intervention
Participants will receive 30 sessions of transcranial direct current stimulation applied over the left dorsolateral prefrontal cortex. Stimulation will be delivered at 2 mA for 20 minutes per session, once daily, five days per week, under supervision of trained healthcare professionals.
Устройство: Transcranial Direct Current Stimulation
Transcranial direct current stimulation will be delivered using a constant-current stimulator through surface electrodes placed over the scalp. The anode will be positioned over the left dorsolateral prefrontal cortex, corresponding to F3 according to the international 10-20 EEG system, and the cathode will be placed over the contralateral supraorbital region. Each session will be delivered at 2 mA for 20 minutes. Participants will complete 30 sessions.
Другие имена:
  • tDCS
  • Неинвазивная стимуляция мозга
  • EPTE Bipolar tDCS device

Что измеряет исследование?

Первичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Change in EuroQol 5-Dimension 5-Level Questionnaire Score
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Health-related quality of life will be assessed using the EuroQol 5-Dimension 5-Level questionnaire (EQ-5D-5L). The EQ-5D-5L assesses five health dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each rated across five levels of severity. Higher scores or index values reflect better health status, depending on the scoring method used. Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Modified Fatigue Impact Scale Score
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Fatigue will be assessed using the Modified Fatigue Impact Scale (MFIS). The MFIS assesses the impact of fatigue on physical, cognitive, and psychosocial functioning. The total score ranges from 0 to 84, with higher scores indicating greater fatigue impact. Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Montreal Cognitive Assessment Score
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Global cognitive function will be assessed using the Montreal Cognitive Assessment (MoCA). The MoCA evaluates cognitive domains including attention, memory, language, visuospatial abilities, executive function, abstraction, calculation, and orientation. The total score ranges from 0 to 30, with higher scores indicating better cognitive performance. Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Short Form-36 Health Survey Score
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Health-related quality of life will be assessed using the Short Form-36 Health Survey (SF-36). The SF-36 evaluates eight domains of health-related quality of life: physical functioning, role limitations due to physical health, role limitations due to emotional problems, energy/fatigue, emotional well-being, social functioning, pain, and general health. Scores are transformed to a 0-100 scale, with higher scores indicating better health-related quality of life. Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Verbal Fluency Task Performance
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Verbal fluency will be assessed using verbal fluency tasks. Performance will be evaluated based on the number of correct words generated within the specified time period. Higher scores indicate better verbal fluency performance. Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Stroop Test Performance
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Executive function, inhibitory control, and cognitive flexibility will be assessed using the Stroop test. Performance will be evaluated using test-specific measures such as response accuracy and/or completion time. Better performance is reflected by higher accuracy and/or shorter completion time, depending on the scoring method used. Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention

Вторичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
Change in Brain Metabolism
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Brain metabolism will be assessed using positron emission tomography-computed tomography (PET-CT). Changes from baseline to post-intervention will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Heart Rate Variability
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Autonomic nervous system activity will be assessed using heart rate variability (HRV) recorded under resting conditions. Time-domain, frequency-domain, and non-linear HRV indices will be evaluated to characterize changes in autonomic regulation.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Endurance Capacity
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Endurance capacity will be assessed using the Ekblom-Bak submaximal cycle ergometer test. Heart rate responses, perceived exertion, estimated maximal oxygen uptake, and internal load will be evaluated under standardized conditions.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Handgrip Strength
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Upper-limb muscle strength will be assessed using handgrip dynamometry. Participants will perform three maximal attempts, and the highest value will be used for analysis.
Baseline and 3 days after completion of the 30-session tDCS intervention
Change in Lower-Limb Neuromuscular Performance
Временное ограничение: Baseline and 3 days after completion of the 30-session tDCS intervention
Lower-limb neuromuscular performance will be assessed using the countermovement jump test performed on a force platform. Variables related to force and power production will be evaluated.
Baseline and 3 days after completion of the 30-session tDCS intervention
Tolerability of the tDCS Intervention
Временное ограничение: During each tDCS session throughout the 30-session intervention period
Tolerability of the tDCS intervention will be assessed during each stimulation session using session monitoring records and participant reports. Tolerability will be evaluated based on the number of completed tDCS sessions out of the 30 scheduled sessions and the participant's ability to complete each session without clinically relevant discomfort. A higher number of completed sessions indicates greater intervention tolerability
During each tDCS session throughout the 30-session intervention period
Adverse Effects Related to tDCS
Временное ограничение: During each tDCS session throughout the 30-session intervention period
Adverse effects related to tDCS will be monitored and recorded at each stimulation session. Potential adverse effects include tingling, itching, headache, discomfort, burning sensation, dizziness, or transient erythema at the electrode site. The presence, type, and severity of adverse effects will be documented. Severity will be classified as mild, moderate, or severe.
During each tDCS session throughout the 30-session intervention period

Соавторы и исследователи

Здесь вы найдете людей и организации, участвующие в этом исследовании.

Спонсор

University of Las Palmas de Gran Canaria

Соавторы

Canary Islands Health Service
Fundación Canaria Instituto de Investigación Sanitaria de Canarias

Следователи

  • Главный следователь: Juan Francisco Vigueras, MD, Canary Islands Health Service

Даты записи исследования

Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.

Изучение основных дат

Начало исследования (Оцененный)

15 сентября 2026 г.

Первичное завершение (Оцененный)

22 декабря 2027 г.

Завершение исследования (Оцененный)

1 марта 2028 г.

Даты регистрации исследования

Первый отправленный

11 июля 2026 г.

Впервые представлено, что соответствует критериям контроля качества

11 июля 2026 г.

Первый опубликованный (Действительный)

16 июля 2026 г.

Обновления учебных записей

Последнее опубликованное обновление (Действительный)

22 июля 2026 г.

Последнее отправленное обновление, отвечающее критериям контроля качества

19 июля 2026 г.

Последняя проверка

1 июля 2026 г.

Дополнительная информация

Термины, связанные с этим исследованием

Ключевые слова

Дополнительные соответствующие термины MeSH

Другие идентификационные номера исследования

  • NEUROSTIM-LC-2026
  • CGC-2025-10415 (Другой идентификатор: Fundación Canaria Instituto de Investigación Sanitaria de Canarias (FIISC))

Информация о лекарствах и устройствах, исследовательские документы

Изучает лекарственный продукт, регулируемый FDA США.

Нет

Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.

Нет

Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .

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