Understanding the features of Restless Legs Syndrome.

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the evolution of symptoms in patients with Restless Legs Syndrome (RLS) by examining clinical, biological, and pharmacological factors. It will involve a large cohort of RLS patients who are members of the French RLS association and other European RLS associations. The study will focus on how RLS phenotype, comorbidities, and medications influence the severity of symptoms over time. By gathering data from this population, the study seeks to provide insights into the natural course of RLS and its complications.

Why it matters

Who can join: the full rules

Inclusion criteria:

* Adults subjects
* Restless legs syndrome diagnosis
* Member of the restless legs syndrome association
* French speaking
* Able to understand the study
* Signed written informed consent
* Affiliated to social security

Exclusion criteria:

\- Vulnerable subject : subject deprived of liberty or protected by law (trusteeship, legal guardianship)

Where it's running

• Uhmontpellier
  Montpellier, France Recruiting

Study contacts

• Study coordinator: Sofiene Chenini, MD
• Email: sofienechenini@hotmail.com
• Phone: 467332237

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• Using mobile technology to assess symptoms in patients with Restless Legs Syndrome

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.