Restless Legs Syndrome Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are 18 years of age or older
- You have been diagnosed with Restless Legs Syndrome (RLS)
- Your RLS symptoms are rated as moderate to severe (based on a standard scoring system used by doctors)
- You are not currently receiving any treatment for your RLS
- You have not been doing regular physical activity (at least 30 minutes a day) on more than 2 days per week for the past six months
- You are able to walk on your own without using a cane, walker, or wheelchair
- You are willing to complete all measurements and participate in the full exercise program
Who may not be able to join:
- You have a condition that could cause similar symptoms to RLS or trigger RLS as a side effect — for example, iron deficiency anemia, nerve pain in the back, swelling in the legs, nerve damage in the hands or feet, or diabetes
- You have been assessed as being at moderate or high risk when doing intense or maximum-effort exercise (confirm with trial site)
⚠️ Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Emmanuel Mignot, MD, PhD, Stanford University
Phone: (650) 725-6517
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Protein Expression Profile; Protein Expression Profile
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.