Join the EASE-RLS Clinical Study for Restless Leg Syndrome (RLS)

The REST-RLS Clinical study is evaluating the long-term effectiveness and safety of the Nidra TOMAC (Tonic Motor Activation) System, a non-drug treatment designed to help reduce symptoms of Restless Leg Syndrome (RLS) in adults.

This study is conducted entirely online and involves completing electronic questionnaires about your health and experiences. The purpose of the study is to assess the long-term effectiveness and safety of the TOMAC System in a Real-World population. Participation in this study would last approximately 1-2 years. You will be compensated for all visits completed.

To see if you might qualify for this study, you will need to answer some questions about your health history and present condition. Some of these questions may be sensitive, you may stop at any time. If you are eligible or agree to have your medical information obtained during this pre-screening, it will be stored for other studies, and your information will be kept in a binder at a locked location and/or in a password-protected database for two years. This section is expected to take about 10-15 minutes.

Schedule an appointment: https://bookings.cloud.microsoft/book/TheEASErlsstudy@noctrixhealth.com/?ismsaljsauthenabled=true

Email: ease-rlsstudy@noctrixhealth.com

Phone: (925) 243-7641

Sign up below if you're interested in taking part and see if you might qualify for the study.

Your email address

Phone Number

I consent to receive automated SMS messages about this research study at the phone number provided above. This text consent is not required to sign up for this research study and consent may be revoked at any time. Standard Msg & data rates apply. Message frequency varies. Reply SMS HELP for text support and STOP to unsubscribe at any time.

I have read and accept the Privacy Policy and Terms of Use.

Participant Benefits

Contribution to research that may benefit future RLS patients
Potential reduction in RLS symptoms and improved sleep quality
Objective device usage and leg-movement data collection that may inform personalized care
Individualized device titration and training on safe/effective use

Privacy:

Your privacy is important to us. The information you provide (such as your email address and mobile number) will be used solely for study-related purposes, including communication and survey reminders. Your information will not be shared with third parties for marketing or promotional purposes. All data will be handled in accordance with applicable privacy regulations.

Terms of Use:

a. Program Name: REST-RLS Clinical Study for Restless Leg Syndrome (RLS)
b. Message Frequency: You will receive daily automated SMS based on your specific study schedule.
c. Costs: Message and data rates may apply.
d. Support: For assistance contact one of the study coordinators at the phone number(s) listed in this document. Email- restrlsstudy@noctrixhealth.com
e. Opt-Out: You can cancel the SMS service at any time. Reply STOP to stop SMS
f. Carrier Liability: Carriers are not liable for any delayed or undelivered messages

EASE-RLS Study