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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04799418
Other study ID # SNS-PD-003
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date September 15, 2022
Est. completion date September 2024

Study information

Verified date October 2022
Source Scion NeuroStim
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study seeks to establish the safety and efficacy of extended twice daily treatments for treating symptoms associated with PD. Only participants who completed the STEM-PD RCT trial are eligible for the OLE.


Description:

Up to 220 participants will enter an open label extension (OLE) study during which all study participants will receive treatment for 12 weeks (84 days). Study participants will be followed for 16 weeks (112 days) post treatment-cessation and then the twice daily treatments will be re-introduced for the final 8 weeks (56 days).


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 220
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Completion of the study activities in the STEM-PD RCT trial. l. - Participants must be willing and able to give consent to participate in the study trial. Exclusion Criteria: - Participant anticipates being unable to attend all visits and complete all study activities in both the RCT and OLE study trial. - Women of child-bearing potential who are pregnant or plan to become pregnant during the course of the RCT or OLE study trial.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Open Label Extension Study
This study will investigate the safety and efficacy of extended treatments for the management of symptoms related to PD.

Locations

Country Name City State
United States University of New Mexico Albuquerque New Mexico
United States Parkinson's Disease and Movement Disorder of Boca Raton Boca Raton Florida
United States Medical University of South Carolina Charleston South Carolina
United States Cleveland Clinic Cleveland Ohio
United States Quest Research Farmington Hills Michigan
United States Mercy Health Saint Mary's Grand Rapids Michigan
United States Houston Methodist Neurological Institute Houston Texas
United States University of Kansas Medical Center - Parkinson's Disease Center Kansas City Kansas
United States Cedars-Sinai Medical Center Los Angeles California
United States Veracity Neuroscience Memphis Tennessee
United States Riverside Neurology Specialists Newport News Virginia
United States Headlands Research Orlando Orlando Florida
United States Meridian Clinical Research Raleigh North Carolina
United States Movement Disorder Center of Arizona Scottsdale Arizona
United States University of South Florida Tampa Florida

Sponsors (1)

Lead Sponsor Collaborator
Scion NeuroStim

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Change from baseline in the Mini-Balance Evaluation Systems Test a measure of dynamic balance, functional mobility, and gait. This measure will be evaluated as a safety outcome to assess whether device therapy negatively impacts balance or gait for participants with Parkinson's disease (day 197 score) 8 months
Other Change from baseline in the Montreal Cognitive Assessment a screening instrument used to facilitate the assessment of cognitive impairment. 8 months
Other Change from baseline in the Oral Symbol Digit Modality Test a brief and commonly used tests to evaluate processing speed 8 months
Other Change from baseline in the Parkinson's Disease Sleep Scale an assessment to quantify nocturnal sleep issues in Parkinson's disease 8 months
Other Change from baseline in Epworth Sleepiness Scale a brief measure that is commonly used to assess daytime sleepiness 8 months
Other Change from baseline in the Parkinson Anxiety Scale a brief questionnaire to detect anxiety severity in Parkinson's disease 8 months
Other Change from baseline in the Functional Assessment of Chronic Illness Therapy - Fatigue Scale a measure of an individual's level of fatigue during their usual daily activities over the past week 8 months
Other Change from baseline in the Geriatric Depression Scale-15 a short questionnaire for assessing depression in older adults 8 months
Other Change from baseline in the MDS-NMS Non-Motor Fluctuations a rater completed assessment evaluating fluctuations of non-motor symptoms in Parkinson's disease 8 months
Other Change from baseline in the Unified Parkinson's Disease Rating Scale Part IV an assessment of complications of anti-Parkinsonian therapies 8 months
Other Change from baseline in a Non-Motor Symptom focused Clinical Global Impression-Improvement clinician assessment the extent of clinically meaningful change that has occurred as it relates to the patient's non-motor symptoms 8 months
Other Change from baseline in the Zarit Burden Interview measure of caregiving burden completed by caregivers 8 months
Other Change from baseline in the Patient Reported Outcome - Parkinson's Disease a self-rating tool to assess symptom severity in Parkinson's disease 8 months
Other Change from baseline in The Modified Schwab and England Activities of Daily Living Scale a clinical outcome assessment of an individual's ability to function independently in activities of daily living 8 months
Other Change from baseline in EncephaLogTM 3 meter Timed Up and Go Test smart phone application assessment that provides indication of risk of falls in adults 8 months
Other Change from baseline in EncephaLogTM finger tapping test smart phone application providing a quantitative measure of bradykinesia 8 months
Other Change from baseline in EncephaLogTM 10m Timed Up and Go (10m TUG) smart phone application that measures gait and that provides indication of risk of falls in adults 8 months
Other Change from baseline in Unified Parkinson's disease Rating Scale Part I (UPDRS I) a measure of mentation, behavior, and mood in Parkinson's disease 8 months
Other Change from baseline in Hoehn & Yahr (H&Y) staging tool describing the level of disability in Parkinson's disease 8 months
Other Change from baseline in Patient Global Impression of Improvement a patient determined scale to assess how much their illness has improved or worsened relative to a baseline state at the beginning of the intervention 8 months
Primary Change from baseline in The International Parkinson and Movement Disorder Society - Non-Motor Rating Scale (MDS-NMS) Total Score The MDS- NMS is 52-item rater-administered scale used to assess a wide range of non-motor symptoms in Parkinson's disease. Scores range between 0-832, with the higher score indicating greater non-motor symptom burden. (day 197 score) 8 months
Secondary Change from baseline in The International Parkinson and Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part II The MDS- UPDRS Part II is a 13- item patient-reported assessment of activities of motor aspects of experiences of daily living. Scores range between 0-52, with the higher score indicating greater impairment to activities of daily living. (day 197 score) 8 months
Secondary Change from baseline in the Clinical Global Impression - Improvement (CGI-I) The CGI-I is a clinician assessment the extent of clinically meaningful change that has occurred in the patient's illness at day 113 relative to a baseline state (assessed at day 29). Changes in all aspects of Parkinson's disease (e.g., motor symptoms, non-motor symptoms and complications of anti-Parkinsonian medications) are considered. 8 months
Secondary Change from baseline in the MDS-UPDRS Part III The MDS-UPDRS Part III is a 33-item assessment of motor function evaluated by a trained blinded rater. Scores range between 0-132 with higher scores indicating more sever motor symptoms. (day 197 score) 8 months
Secondary Change from baseline in the Parkinson's Disease Quality of Life Questionnaire Summary Index (PDQ-39 SI) The PDQ-39 SI is a 39-item patient-reported quality of life measure that assesses how often people living with PD are affected across 8 dimensions of daily living. Scores range from 0-100, with the higher scores indicating worse perception of quality of life. (day 197 score) 8 months
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