Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT05070013

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

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

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)
Not Eligible

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

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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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