Pleasanton, CANCT07675109Now EnrollingIRB Ready

Restless Legs Syndrome (RLS) Clinical Trial in Pleasanton, CA

Access cutting-edge restless legs syndrome (rls) treatment through this clinical trial at a research site in Pleasanton. Study-provided care at no cost to qualified participants.

Sponsored by Noctrix Health, Inc.

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Expert Care in Pleasanton

Access restless legs syndrome (rls) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related restless legs syndrome (rls) treatment provided free

Apply for This Pleasanton Location

Check if you qualify for this restless legs syndrome (rls) clinical trial in Pleasanton, CA

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Pleasanton

    Convenient for CA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Pleasanton site if eligible
  4. 4Begin participation

About This Restless Legs Syndrome (RLS) Study in Pleasanton

This study assesses the tolerability, safety, and impact of an investigational medical device on restless legs syndrome symptoms. The IRB has established that the investigational device is non-significant risk.

Sponsor: Noctrix Health, Inc.

Who Can Participate

Inclusion Criteria

Subject has signed a valid, IRB-approved informed consent form, can understand the requirements of the study and instructions for device usage, and can converse in English
Subject has received a medical diagnosis of primary restless legs syndrome (RLS).
Subject agrees to not change dosage or schedule of any medications that are known to impact RLS symptoms during the study, including RLS medications, antidepressants, sleep medications, or sedative antihistamines or treatments such as CPAP (continuous positive airway pressure).
Subject reports that RLS symptoms are most significant in lower legs and/or feet.
Subject reports that RLS symptoms caused awakenings or interfered with falling back asleep at least 3 nights per week during the month prior to study entry.
The subject possesses the necessary equipment, internet/phone accessibility, and communication ability to complete electronic questionnaires and respond to electronic communications and phone calls from the research staff throughout the in-home portion of the study.
Subject has moderate-severe RLS symptoms as defined by a score of 15 or greater points on IRLS (International Restless Legs Syndrome Study Group Rating Scale).
Subject is 21 years of age or older.

Exclusion Criteria

The subject has an active medical device implant anywhere in the body (including but not limited to pacemakers, spinal cord stimulators, deep brain stimulators).
The subject has a metal implant at the site of the study device electrode application (not including knee replacements).
The subject has been diagnosed with epilepsy or other seizure disorder.
The subject has a moderate or severe cognitive disorder or mental illness that would affect his or her ability to participate in the study.
The subject has a known allergy to device materials, electrode gel, polyurethane foam, or lycra (or a severe previous reaction to medical adhesives or bandages).
Subject has any of the following at or near the location of device application: Acute injury, Cellulitis, Open sores
The subject is unable or unwilling to comply with study requirements.
The subject has a medical condition not listed above that may put them at risk.
Subject has prior experience with neurostimulation devices developed by the study sponsor
Subject has a primary sleep disorder other than RLS that significantly interferes with sleep at the present time (e.g. obstructive sleep apnea stably controlled via CPAP would not be an exclusion).
On nights with no RLS symptoms (if any), subject reports typical sleep onset latency of \>60min.
Subject has severe peripheral neuropathy affecting the lower legs and/or subject has neuropathy and is unable to clearly distinguish between symptoms of neuropathy and symptoms of RLS.
Subject reports a habitual sleep schedule that is not primarily aligned with nighttime hours (bedtime 8:00pm-2:00am and morning awakening 4:00am-11:00am), or reports that bedtime regularly varies by more than 4 hours (e.g., due to shift work or an inconsistent sleep schedule).
Subject is taking an unstable or inconsistent dose or schedule of medication that is likely to impact RLS symptoms or sleep, such as RLS medications, antidepressants, sleep medications, or sedative antihistamines.
Subject has changed dose or schedule of medication or treatment that is likely to impact RLS symptoms or sleep in the past 30 days, such as RLS medications, antidepressants, sleep medications, or sedative antihistamines or treatments such as CPAP.
During initial device set-up, device does not properly fit the subject or calibrated intensity settings are outside of operational range

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Pleasanton?

Yes, this clinical trial (NCT07675109) has an active research site in Pleasanton, CA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Restless Legs Syndrome (RLS) Treatment Options in Pleasanton, CA

If you're searching for restless legs syndrome (rls) treatment options in Pleasanton, CA, this clinical trial (NCT07675109) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Pleasanton research site is actively enrolling participants for this clinical trial. You'll receive care from experienced restless legs syndrome (rls) specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all restless legs syndrome (rls) clinical trials near you to find additional studies recruiting in your area.

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