+1 877 705 191424 / 7
HIPAA Compliant
ISO 27001 Certified

Actively Recruiting

Age: 18Years +
All Genders
ID05044520

Clinical Features Associated With Restless Legs Syndrome Clin-RLS

Led by University Hospital, Montpellier · Updated on 2021-09-24

2000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating the clinical features and progression of Restless Legs Syndrome RLS, a chronic neurological condition causing an urge to move the legs at night, leading to sleep problems, daytime sleepiness, and reduced quality of life. This observational study aims to assess how RLS symptom severity changes over time in relation to different RLS types, other health conditions, and medications used by patients, involving members of French and European RLS associations. The study does not involve experimental treatments but observes patients who are already diagnosed with RLS and are members of patient associations. It will collect clinical and biological data as well as information on current RLS medications. The study will measure symptom severity and related impacts using various rating scales and questionnaires during scheduled assessments. Participants will be asked to complete several rating scales including the International Restless Legs Syndrome Study Group rating scale and questionnaires assessing sleep issues, depression, quality of life, and fall risk. The study will monitor these measures over time to understand symptom progression. Participants must be adults, able to communicate in French, and affiliated with social security. The study duration extends through to 2027, with ongoing data collection and follow-up.

CONDITIONS

Brief Title

Clinical Features Associated With Restless Legs Syndrome.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult subjects
  • Diagnosed with restless legs syndrome
  • Member of a restless legs syndrome patient association
  • Able to speak and understand French
  • Able to understand the study details
  • Signed written informed consent
  • Affiliated with social security
Not Eligible

You will not qualify if you...

  • Subjects who are vulnerable, such as those deprived of liberty or under legal guardianship or trusteeship

Research Team

S

Sofiene Chenini, MD

Y

Yves DAUVILLIERS, MD PhD

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here