Transcutaneous Auricular Vagus Nerve Stimulation in Psoriatic Arthritis
11 июня 2026 г. обновлено: Marmara University
The Effect of Transcutaneous Auricular Vagus Nerve Stimulation on Disease Activity and Related Clinical Parameters in Patients With Psoriatic Arthritis
This prospective single-center interventional study aims to investigate the effects of transcutaneous auricular vagus nerve stimulation (taVNS) on disease activity, pain, quality of life, autonomic dysfunction symptoms, and inflammatory biomarkers in patients with psoriatic arthritis (PsA).
Participants diagnosed with PsA according to the Classification Criteria for Psoriatic Arthritis (CASPAR) will undergo non-invasive auricular vagus nerve stimulation using the Vagustim device.
Clinical outcomes including the Disease Activity Index for Psoriatic Arthritis (DAPSA), Ankylosing Spondylitis Disease Activity Score based on C-reactive protein (ASDAS-CRP), Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), pain scores, sleep quality, quality of life, anxiety/depression, and inflammatory markers including C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) will be evaluated before and after treatment.
Обзор исследования
Статус
Рекрутинг
Условия
Вмешательство/лечение
Подробное описание
Psoriatic arthritis (PsA) is a chronic, immune-mediated inflammatory disease characterized by heterogeneous clinical manifestations including peripheral arthritis, spondylitis, enthesitis, and dactylitis. Although currently available pharmacological therapies such as conventional synthetic disease-modifying antirheumatic drugs (DMARDs), biologic DMARDs, and targeted synthetic DMARDs are effective in many patients, treatment response may vary, and long-term use may be associated with adverse effects, infection risk, high cost, and treatment resistance.
Recent neuroimmunology studies have demonstrated that the vagus nerve plays a significant role in modulation of inflammatory responses through the cholinergic anti-inflammatory pathway. Transcutaneous auricular vagus nerve stimulation (taVNS) is a non-invasive neuromodulation technique targeting the auricular branch of the vagus nerve and has emerged as a potentially safe and reproducible therapeutic approach in inflammatory disorders.
Previous studies have shown that vagus nerve stimulation may reduce inflammatory cytokine production and improve clinical outcomes in diseases such as rheumatoid arthritis and systemic lupus erythematosus. However, evidence regarding the clinical and biological effects of taVNS in patients with psoriatic arthritis remains limited.
The aim of this prospective, single-center, single-arm interventional study is to evaluate the effects of taVNS on disease activity, pain, functional status, quality of life, autonomic dysfunction symptoms, sleep quality, anxiety/depression symptoms, and inflammatory biomarkers including C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR) in patients with PsA diagnosed according to the Classification Criteria for Psoriatic Arthritis (CASPAR).
Eligible participants aged 18-65 years with moderate-to-severe disease activity will undergo non-invasive auricular vagus nerve stimulation using the Vagustim device. Electrodes will be placed on the tragus and cymba conchae regions of the auricle, and electrical stimulation will be applied for 20 minutes per session according to predefined stimulation parameters.
Clinical assessments including the Disease Activity Index for Psoriatic Arthritis (DAPSA), Ankylosing Spondylitis Disease Activity Score based on C-reactive protein (ASDAS-CRP), Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), Visual Analog Scale (VAS) pain scores, the Short Form-12 Health Survey (SF-12), Pittsburgh Sleep Quality Index (PSQI), Composite Autonomic Symptom Score-31 (COMPASS-31), Hospital Anxiety and Depression Scale (HADS), and Fibromyalgia Rapid Screening Tool (FiRST) will be evaluated before and after treatment.
Тип исследования
Интервенционный
Регистрация (Оцененный)
15
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: Zeynep M Kurt, MD
- Номер телефона: +90 533 485 59 11
- Электронная почта: kurtzeynepmelis@gmail.com
Места учебы
-
-
-
Istanbul, Турция (Туркие), 34899
- Рекрутинг
- Marmara University Pendik Training and Research Hospital
-
-
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:
- Diagnosis of psoriatic arthritis according to the CASPAR criteria
- Age between 18 and 65 years
- Stable treatment regimen for at least 12 weeks prior to enrollment
- Visual Analog Scale (VAS) pain score ≥4 on a 0-10 scale
- Moderate-to-high disease activity according to the Disease Activity Index for Psoriatic Arthritis (DAPSA)
- Ability and willingness to provide written informed consent
Exclusion Criteria:
- Presence of an implanted cardiac device (e.g., pacemaker, implantable cardioverter-defibrillator) or implanted neurostimulator
- History of epilepsy or other uncontrolled neurological disorders
- Active severe infection or immunosuppressive condition (e.g., sepsis)
- Pregnancy or breastfeeding
- Presence of deep auricular injury, previous ear surgery, or active skin lesions involving the auricle
- Inability to comply with the treatment protocol or history of severe psychiatric disorders
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: taVNS Group
Participants with psoriatic arthritis will receive transcutaneous auricular vagus nerve stimulation (taVNS) using the Vagustim device.
Electrical stimulation will be applied through electrodes placed on the tragus and cymba conchae regions of the auricle for 20 minutes per session over a 10-day treatment period.
|
Non-invasive transcutaneous auricular vagus nerve stimulation (taVNS) will be administered using the Vagustim device.
Electrodes will be placed on the tragus and cymba conchae regions of the auricle, which are anatomically associated with the auricular branch of the vagus nerve.
Electrical stimulation will be applied for 20 minutes per session over a 10-day treatment period while participants are in a seated position.
All procedures will be performed according to standardized stimulation parameters and patient safety protocols.
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change in Disease Activity According to Disease Activity Index for Psoriatic Arthritis (DAPSA)
Временное ограничение: Baseline, Day 10, and Month 3
|
Disease activity will be assessed using the Disease Activity Index for Psoriatic Arthritis (DAPSA).
Higher scores indicate greater disease activity and worse clinical status.
|
Baseline, Day 10, and Month 3
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Change in Disease Activity According to Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)
Временное ограничение: Baseline, Day 10, and Month 3
|
Disease activity and symptom severity will be assessed using the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).
Scores range from 0 to 10, with higher scores indicating greater disease activity and symptom burden.
|
Baseline, Day 10, and Month 3
|
|
Change in Disease Activity According to Ankylosing Spondylitis Disease Activity Score Based on C-Reactive Protein (ASDAS-CRP)
Временное ограничение: Baseline, Day 10, and Month 3
|
Disease activity will be evaluated using the Ankylosing Spondylitis Disease Activity Score based on C-reactive protein (ASDAS-CRP).
Higher scores indicate greater inflammatory disease activity and worse clinical status.
|
Baseline, Day 10, and Month 3
|
|
Change in Pain Severity According to Visual Analog Scale (VAS)
Временное ограничение: Baseline, Day 10, and Month 3
|
Pain severity will be assessed using the Visual Analog Scale (VAS), a validated self-reported measure in which participants rate their pain intensity on a scale ranging from 0 (no pain) to 10 (worst imaginable pain).
|
Baseline, Day 10, and Month 3
|
|
Change in Global Disease Assessment According to Visual Analog Scale Global Assessment (VAS Global)
Временное ограничение: Baseline, Day 10, and Month 3
|
Participants' overall perception of disease activity will be assessed using the Visual Analog Scale Global Assessment (VAS Global), scored from 0 to 10. Higher scores indicate greater perceived disease activity and worse health status.
|
Baseline, Day 10, and Month 3
|
|
Change in Disease Activity According to Physician Global Assessment (PGA)
Временное ограничение: Baseline, Day 10, and Month 3
|
Overall disease activity will be evaluated using the Physician Global Assessment, scored from 0 to 10. Higher scores indicate greater disease activity and worse clinical status as assessed by the physician.
|
Baseline, Day 10, and Month 3
|
|
Change in Psoriasis Severity According to Psoriasis Area and Severity Index (PASI)
Временное ограничение: Baseline, Day 10, and Month 3
|
Psoriasis severity and extent of skin involvement will be assessed using the Psoriasis Area and Severity Index (PASI).
Scores range from 0 to 72, with higher scores indicating more severe psoriasis and greater skin involvement.
|
Baseline, Day 10, and Month 3
|
|
Change in Quality of Life According to Short Form-12 Health Survey (SF-12)
Временное ограничение: Baseline, Day 10, and Month 3
|
Health-related quality of life will be assessed using the Short Form-12 Health Survey (SF-12).
Scores range from 0 to 100, with higher scores indicating better health-related quality of life.
|
Baseline, Day 10, and Month 3
|
|
Change in Sleep Quality According to Pittsburgh Sleep Quality Index (PSQI)
Временное ограничение: Baseline, Day 10, and Month 3
|
Sleep quality and sleep disturbances will be assessed using the Pittsburgh Sleep Quality Index (PSQI).
Scores range from 0 to 21, with higher scores indicating poorer sleep quality and greater sleep disturbance.
|
Baseline, Day 10, and Month 3
|
|
Change in Autonomic Dysfunction Symptoms According to Composite Autonomic Symptom Score-31 (COMPASS-31)
Временное ограничение: Baseline, Day 10, and Month 3
|
Autonomic nervous system symptoms will be assessed using the Composite Autonomic Symptom Score-31 (COMPASS-31).
Scores range from 0 to 100, with higher scores indicating greater autonomic symptom burden and worse autonomic dysfunction.
|
Baseline, Day 10, and Month 3
|
|
Change in Anxiety and Depression Symptoms According to Hospital Anxiety and Depression Scale (HADS)
Временное ограничение: Baseline, Day 10, and Month 3
|
Symptoms of anxiety and depression will be evaluated using the Hospital Anxiety and Depression Scale (HADS).
Total scores range from 0 to 42, with higher scores indicating greater psychological distress.
|
Baseline, Day 10, and Month 3
|
|
Change in Fibromyalgia Symptoms According to Fibromyalgia Rapid Screening Tool (FiRST)
Временное ограничение: Baseline, Day 10, and Month 3
|
Fibromyalgia-related symptoms will be screened using the Fibromyalgia Rapid Screening Tool (FiRST).
Scores range from 0 to 6, with higher scores indicating a greater likelihood of fibromyalgia.
|
Baseline, Day 10, and Month 3
|
|
Change in C-Reactive Protein (CRP) Level
Временное ограничение: Baseline, Day 10, and Month 3
|
Inflammatory activity will be evaluated by measuring serum C-reactive protein (CRP) levels.
Higher values indicate greater systemic inflammation.
|
Baseline, Day 10, and Month 3
|
|
Achievement of Minimal Disease Activity (MDA)
Временное ограничение: Baseline, Day 10, and Month 3
|
Minimal Disease Activity (MDA) status will be assessed as a composite outcome according to established Psoriatic Arthritis Minimal Disease Activity criteria.
Participants will be classified as achieving or not achieving MDA at each assessment time point.
|
Baseline, Day 10, and Month 3
|
|
Change in Functional Status According to Health Assessment Questionnaire (HAQ)
Временное ограничение: Baseline, Day 10, and Month 3
|
Functional disability and daily living activities will be evaluated using the Health Assessment Questionnaire (HAQ).
Scores range from 0 to 3, with higher scores indicating greater functional impairment and disability.
|
Baseline, Day 10, and Month 3
|
|
Change in Erythrocyte Sedimentation Rate (ESR)
Временное ограничение: Baseline, Day 10, and Month 3
|
Inflammatory activity will be evaluated by measuring erythrocyte sedimentation rate (ESR).
Higher values indicate greater systemic inflammation.
|
Baseline, Day 10, and Month 3
|
Соавторы и исследователи
Здесь вы найдете людей и организации, участвующие в этом исследовании.
Спонсор
Следователи
- Главный следователь: Halise Hande Gezer, MD, Associate Professor, Marmara University Faculty of Medicine
Публикации и полезные ссылки
Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.
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 (Действительный)
2 июня 2026 г.
Первичное завершение (Оцененный)
2 июня 2027 г.
Завершение исследования (Оцененный)
2 августа 2027 г.
Даты регистрации исследования
Первый отправленный
2 июня 2026 г.
Впервые представлено, что соответствует критериям контроля качества
11 июня 2026 г.
Первый опубликованный (Действительный)
17 июня 2026 г.
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
17 июня 2026 г.
Последнее отправленное обновление, отвечающее критериям контроля качества
11 июня 2026 г.
Последняя проверка
1 июня 2026 г.
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- Marmara FTR ZMK 01
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
НЕТ
Описание плана IPD
Individual participant data are not planned to be shared.
Aggregated results will be reported in publications.
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. .