Ecological Momentary Assessment in Patients With Restless Legs Syndrome (DAILY-REST)
Restless Legs Syndrome
About this trial
This is an interventional other trial for Restless Legs Syndrome focused on measuring Restless Legs Syndrome, Risk Factor, Ecological Momentary Assessment, Mobile Technology, Sleep, Actigraphy
Eligibility Criteria
Inclusion Criteria: Patient over 18 years old and less than 65 Any patient with a diagnosis of idiopathic RLS based on medical history and the presence of the 5 RLS diagnostic criteria Normal clinical examination Person affiliated or benefiting from a social security scheme Free, informed and written consent signed by the participant and the investigator (no later than the day of inclusion and prior to any review required by the research). Exclusion Criteria: Any significant psychiatric illness (schizophrenia, bipolar disorder, severe depression, dementia, obsessive compulsive disorder, attention-deficit/hyperactivity disorder ...) or mood disorder History or presence of chronic pain other than that associated with RLS, history of epilepsy or serious head injury, history of peripheral neuropathy, diabetes Clinically significant sleep apnea, narcolepsy, or any secondary causes of RLS (e.g. chronic renal failure/hemodialysis, pregnancy) Other active clinically significant illness, including unstable cardiovascular, or neoplasic pathology which could interfere with the study conduct or interfere with study assessments or compromise the study participation Pregnant or breastfeeding woman Persons referred to in articles L.1121-5 to L.1121-8 (persons deprived of liberty by judicial or administrative decision, minors, adults subject to a legal protection measure or unable to express their consent).
Sites / Locations
- CHU de Bordeaux - Neurophysiologie Clinique de l'Enfant et de l'Adulte
Arms of the Study
Arm 1
Experimental
Restless Legs Syndrome