Noninvasive Peripheral Nerve Stimulation for Restless Legs Syndrome

Restless Legs Syndrome Clinical Trial

Official title:

Chronic Efficacy and Usability of Transcutaneous Electrical Nerve Stimulation in Subjects With Restless Leg Syndrome (RLS)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04700683
• Other study ID #: RLS-SNS01
• Status: Completed
• Phase: N/A
• Start date: July 14, 2019
• Est. completion date: March 1, 2020

Study information

• Verified date: January 2021
• Source: Noctrix Health, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Prospective multi-site randomized sham-controlled crossover feasibility study evaluating tolerability and efficacy of noninvasive peripheral nerve stimulation (NPNS) for patients with moderate-severe primary Restless Legs Syndrome (RLS). Response to NPNS investigational device was compared to sham control in a 2x2 crossover design such that subjects were assigned to receive 2 weeks of NPNS and 2 weeks of sham, in randomized order.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 43
• Est. completion date: March 1, 2020
• Est. primary completion date: March 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Subject has moderate-severe RLS symptoms as defined by a score of 15 or greater points on IRLS.

• RLS symptoms are primarily noticeable in the subject's lower legs and/or feet.

• Subject reports having a medical diagnosis of primary idiopathic restless legs syndrome (RLS) or Willis-Ekbom Disorder (WED) OR Investigator has diagnosed the subject with primary idiopathic restless legs syndrome (RLS) or Willis-Ekbom Disorder (WED).

• Subject has experienced RLS symptoms at night on 2 or more nights per week during the previous month.

• On typical dose and schedule of RLS medication (if any), subject typically experiences RLS symptoms on 2 or more nights per week.

• RLS symptoms are primarily in the evening and night.

• Subject owns the necessary equipment to respond to texts, phone calls, and video calls.

• Subject is 18 years of age or older when written informed consent is obtained.

• Subject has signed a valid, Institutional Review Board (IRB)-approved informed consent form, can understand the requirements of the study and instructions for device usage, and can converse in English.

Exclusion Criteria:

• Subject has RLS that is known to be caused by another diagnosed condition.

• Subject has active implantable medical devices anywhere in the body (including pacemakers), or passive medical devices implanted in the leg.

• Subject has an uncontrolled sleep disorder other than RLS that significantly interferes with their sleep as determined by the trial director or physician.

• Subject has been diagnosed with one of the following conditions: Epilepsy or other seizure disorder, Cellulitis or open sores of the legs, Renal failure, Iron-Deficiency Anemia, Severe movement disorder symptoms (Parkinson's disease, Huntington's disease, dyskinesia, dystonia), Deep Vein Thrombosis, Stage 4-5 Chronic Kidney Disease, Multiple sclerosis, Current, active or acute or chronic infection other than viral upper respiratory tract infections, A malignancy within the past 5 years (not including basal or squamous cell skin cancer)

• Subject is on dialysis or anticipated to start dialysis while participating in the study

• Subject is allergic to electrode gel, polyurethane foam, or lycra.

• Subject has severe edema in lower legs.

• Subject has failed a nerve conduction study prescribed by a physician or has been diagnosed with severe peripheral neuropathy.

• During Visit 1, subject cannot notice the stimulation at the maximal dose or cannot tolerate the stimulation at the minimal effective dose

• Subject selects Statement 2 or is unable to decide which of the following two statements most closely describe their condition: Statement 1: My symptoms are best characterized by a strong or overwhelming urge to move my legs. Moving my legs often results in temporary relief of that urge. Statement 2: My symptoms are best characterized by involuntary leg spasms that happen at regular intervals. These leg spasms can wake me up in the middle of the night."

• Subject has significantly changed medication dose or schedule of antidepressants, sleep medications, or RLS medications within the past 30 days.

• Recent history of alcohol or recreational drug abuse (within the past 6 months).

• Subject has received an investigational drug or device within the last 30 days or is planning to receive an investigational device during the duration of the study.

• Subject has undergone a major surgery (excluding dental work) in the previous 30 days.

• Subject has another medical condition that may affect validity of the study or put the subject at risk as determined by the investigator.

• Subject is unable or unwilling to comply with study requirements

Related Conditions & MeSH terms

• Psychomotor Agitation
• Restless Legs Syndrome
• Syndrome

Intervention

Device:
• Noctrix Health NPNS device v1.0 - Active
Wearable device programmed to deliver electrical stimulation to peripheral nerves of the lower limbs.
• Noctrix Health NPNS device v1.0 - Sham
Wearable device programmed to deliver sham stimulation.

Locations

Country	Name	City	State
United States	Mark J Buchfuhrer private practice	Downey	California
United States	SRI International Human Sleep Research Lab	Menlo Park	California
United States	Sleep Medicine Specialists of California	San Ramon	California

Sponsors (1)

Lead Sponsor	Collaborator
Noctrix Health, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change to NRS score of RLS severity during SIT procedure	The 60-minute Suggested Immobilization Test (SIT) assesses RLS symptom severity in a controlled procedure in the following three conditions: no device, NPNS device, Sham device. At SIT start and after every 10 minutes, the participant rates average RLS symptom severity from 0-10 on a Numerical Rating Scale (NRS) scale, where 10 is the most severe.	During the 60 minute SIT procedure
Primary	Evaluate the clinical tolerability, usability, and patient response for the prototype device, with the intention of improving overall device performance.	Subject satisfaction and usability questionnaire	Weeks 1-2 of each intervention
Secondary	Change from baseline in International Restless Legs Syndrome Study Group Rating Scale (IRLS) score at week 2	International Restless Legs Syndrome Study Group Rating Scale is a participant-rated questionnaire that rates RLS severity from 0-40, where 40 is the most severe.	Week 2 of each intervention compared to week prior to study entry
Secondary	Change to Summary NRS score of RLS symptom severity	Participant rating of average RLS symptom severity from 0-10 on a Numerical Rating Scale (NRS) scale, where 10 is the most severe. Participants complete a single Summary NRS scale at the end of each 2-week intervention, rating the average RLS symptoms before, during, and after device usage.	Weeks 1-2 of each intervention
Secondary	Change to Daily NRS score of RLS symptom severity	Participant rating of average RLS symptom severity from 0-10 on a Numerical Rating Scale (NRS) scale, where 10 is the most severe. Participants complete the Daily NRS scale each day during each 2-week intervention, rating the RLS symptoms before, during, and after the previous night of device use.	Weeks 1-2 of each intervention
Secondary	Responder rate on CGI-I scale at week 2 relative to baseline	Responder rate is defined as the proportion of responses of "Much Improved" or "Very Much Improved" relative to baseline on the 7-point participated-rated Clinical Global Impressions-Improvement (CGI-I) scale.	Week 2 of each intervention compared to week prior to study entry