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 have been diagnosed with Restless Legs Syndrome (RLS)
- Your RLS medications have not changed significantly in the past 4 weeks
- You are willing and able to follow the study's rules and schedule
- You are a healthy person without RLS (for the healthy comparison group in the study)
- You are able to understand and sign a consent form agreeing to take part
Who may not be able to join:
- You have a mental or physical condition that would stop you from completing the study activities
- You are currently using a device (such as a wearable or medical device) to treat your RLS
- You are not willing or able to follow the study's rules and schedule
- You have another medical condition that the study doctor believes could put you at risk
- You are pregnant, breastfeeding, or trying to become pregnant
- You are currently taking part in, or planning to join, another clinical study that might affect your RLS
- You have any of the following conditions: spinal cord injury, severe nerve damage or nerve root problems, a serious psychiatric or memory/thinking disorder, a history of drug or alcohol abuse in the past year, epilepsy or seizures, an active or ongoing infection (other than a common cold), a cancer diagnosis within the past 5 years (excluding certain minor skin cancers), a severe movement disorder such as Parkinson's disease, deep vein thrombosis (a blood clot in a vein), or multiple sclerosis
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
Phone: 2059343411
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
Changes in H-reflex neurophysiological activity in response to Spinal Cord Stimulation (SCS); Changes in Somatosensory Evoked Potential (SSEP) activity in response to Spinal Cord Stimulation (SCS); Changes in Vibratory Electrophysiological Response Potential (ERP) activity in response to Spinal Cord Stimulation (SCS); Changes in Transcranial Magnetic Stimulation (TMS) activity in response to Spinal Cord Stimulation (SCS)
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.