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Набор скоро начнётся NCT07679087

Study of the Frequency and Characteristics of Pain Symptoms in Restless Legs Syndrome

Наблюдательное RLS

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: Patients with RLS.
Кому может быть актуально
Состояния в реестре: RLS. 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
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

Обзор

Restless Legs Syndrome (RLS) is a neurological disorder affecting between 4% and 29% of adults. It is characterized by an urge to move the legs or other parts of the body, often accompanied by unpleasant and sometimes painful sensations. The pathophysiology of RLS, whether associated with pain or not, remains poorly understood, and only a limited number of studies have specifically investigated this aspect. The aim of this study is to determine the prevalence of the painful component of symptoms in a large cohort of patients with RLS, to further characterize its clinical features, and to assess its impact on patients' quality of life. This work could improve the identification of patients experiencing pain, enhance our understanding of pain characteristics in RLS, and help optimize patient management. Furthermore, in the context of emerging therapeutic approaches such as neuromodulation, a better characterization of pain in RLS may contribute to the development and evaluation of new treatment strategies. This is particularly relevant given the high prevalence of RLS and its substantial impact on patients' quality of life. Participants will be recruited either through their neurologist during routine follow-up visits at the Neurology Department of Clermont-Ferrand University Hospital or through the France Ekbom Association. Individuals interested in participating will be provided with access to the online questionnaire via a QR code or a dedicated web link. One thousand patients will be include in this study (RIPH type 3). The online questionnaire is expected to take approximately 30 minutes to complete. It includes the collection of demographic data (age, sex, lifestyle factors, weight, height, employment status, comorbidities, and dietary habits), as well as questions regarding the patient's medical history and sleep habits. The questionnaire also includes validated instruments assessing sleep, pain, RLS severity, anxiety and depression, and quality of life. At the end of the questionnaire, participants will be invited to take part in an optional ancillary study aimed at validating the French translation of the Restless Legs Syndrome Quality of Life questionnaire (RLS-QOL). Participants who agree to participate will complete the questionnaire once at baseline and will subsequently receive an email reminder to complete it a second time two weeks later. This test-retest procedure will be used to assess the reproducibility of the French-adapted version of the questionnaire.

Вмешательства

  • Другое Patients with RLS
    The online questionnaire is expected to take approximately 30 minutes to complete. It includes the collection of demographic data (age, sex, lifestyle factors, weight, height, employment status, comorbidities, and dietary habits), as well as questions regarding the patient's medical history and sleep habits. The questionnaire also includes validated instruments assessing sleep, pain, RLS severity, anxiety and depression, and quality of life. At the end of the questionnaire, participants will b

Первичные конечные точки

  • Pain evaluation according to the Brief Pain Inventory (PBI) [Срок оценки: at day 0]
Вторичные конечные точки (8)
  • Pain characteristics using the DN4 questionnaire [Срок оценки: at day 0]
  • RLS severity using the International Restless Legs Syndrome Rating Scale (IRLS) [Срок оценки: at day 0]
  • Fibromyalgia using the FIRST (Fibromyalgia Rapid Screening Tool) [Срок оценки: at day 0]
  • Biopsychosocial dimensions of pain according to the Pain Catastrophizing Scale (PCS). [Срок оценки: at day 0]
  • Anxiety and depression using the Hospital Anxiety and Depression Scale (HADS) [Срок оценки: at day 0]
  • Quality of life using the EQ-5D-5L [Срок оценки: at day 0]
  • Daytime sleepiness using Epworth Sleepiness Scale (ESS). [Срок оценки: at day 0]
  • RLS-specific quality of life using the Restless Legs Syndrome Quality of Life questionnaire (RLS-QOL). [Срок оценки: at day 0]

Критерии участия

Критерии включения

  • Male or female participants aged 18 years or older.
  • Diagnosis of Restless Legs Syndrome (RLS) according to the criteria of the International Classification of Sleep Disorders, Third Edition (ICSD-3).
  • French-speaking.

Критерии исключения

  • Patient under guardianship, curatorship, or legal protection measures.
  • Patient who has never had an appointment with a neurologist as part of their SJSR care pathway.

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Другое

Центры проведения

Франция · 1 центр
  • CHU de Clermont-Ferrand — Clermont-Ferrand

Идентификаторы

NCT: NCT07679087 · RNI 2026 FANTINI (PAIN-RLS) · 2026-A00401-50

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗