Actively Recruiting
Adaptive Neurostimulation to Restore Sleep in Parkinson's Disease (Aim 2)
Led by University of Nebraska · Updated on 2025-07-22
20
Participants Needed
2
Research Sites
240 weeks
Total Duration
On this page
Sponsors
U
University of Nebraska
Lead Sponsor
N
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Parkinson's Disease (PD) is the second most common of the age-related neurodegenerative disorders, affecting over 1,900 adults per 100,000 over the age of 80 in the US. The prevalence of sleep dysfunction in PD is estimated at nearly 80-90% which includes sleep fragmentation, insomnia, rapid eye movement (REM or dream sleep) Sleep Behavior Disorder (RBD), Restless legs syndrome (RLS), periodic limb movement, excessive daytime sleepiness, and sleep apnea. Sleep is vital to homeostasis, cognition, and nervous system repair. The dysfunctional sleep accompanying PD adversely affects both motor and non-motor symptoms, resulting in diminished quality of life for both patients and caregivers, including impairments in mood and behavior, and increased morbidity and mortality. Knowledge of sleep phenomenology and pathology in humans has largely been informed by analysis of non-invasive scalp electroencephalogram (EEG), and despite the profound importance of sleep, the underlying neural circuits important for controlling sleep and wakefulness in humans remain poorly understood. This study assesses whether adaptive stimulation of the Subthalamic Nucleus (STN) drives changes in sleep episode maintenance and improves sleep quality. Participants are adults with PD who experience inadequate motor symptom relief, and who have been offered implantation of a deep brain stimulator system targeting STN for the treatment of motor symptoms (standard-of-care). Prior to surgery, participant sleep patterns will be assessed with questionnaires and monitored with a non-invasive watch-like device. Approximately four months after implantation surgery, participants will each receive 2 1-week deep brain stimulation (DBS) treatments and 1 1-week control session with no DBS in random order. Sleep patterns will again be monitored during the treatments and compared to the patterns before surgery.
CONDITIONS
Official Title
Adaptive Neurostimulation to Restore Sleep in Parkinson's Disease (Aim 2)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent
- Diagnosis of idiopathic Parkinson's disease with motor symptoms for at least 4 years
- Severe motor symptoms despite optimized medical therapy warranting deep brain stimulation surgery
- UPDRS-III score off medication between 20 and 80 with improvement on medication, or tremor-dominant PD with significant functional disability
- Stable anti-PD medication dose for 30 days before enrollment
- Approved for Subthalamic Nucleus deep brain stimulation surgery by study team
- No abnormalities on brain MRI suggesting alternate diagnosis or surgery contraindication
- No significant cognitive deficits or depression (BDI-II score 20 or less)
- Age between 18 and 80 years (19 to 80 years in Nebraska)
- Able to receive follow-up neurological care at study site for device lifespan (9 years)
You will not qualify if you...
- Medical conditions increasing surgical risk such as coagulopathy, uncontrolled hypertension, seizures, heart disease, or inability to undergo anesthesia
- Pregnancy without negative urine pregnancy test before surgery
- Significant untreated depression (BDI-II over 20 or GDS over 8)
- Personality or mood disorders interfering with study requirements
- Ongoing treatment with electroconvulsive therapy, transcranial magnetic stimulation, or diathermy
- Existing implanted stimulation system or ferromagnetic metallic implant
- Prior brain surgery
- History or active drug or alcohol abuse
- Parkinson's disease with mild cognitive impairment defined by cognitive testing
- Restless Leg Syndrome
- Obstructive Sleep Apnea
- Inability to perform recharge process for brain stimulation system
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
University of Nebraska Medical Center
Omaha, Nebraska, United States, 68198
Actively Recruiting
2
University of Pennsylvania Health System
Philadelphia, Pennsylvania, United States, 19106
Actively Recruiting
Research Team
D
Dulce Maroni, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
3
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