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NCT07636720Recruiting

Sensing in Sleep Deep Brain Stimulation

Sensing in Sleep and Deep Brain Stimulation

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

Participants in this study have Parkinson's Disease and already have a device, called the Percept RC Deep Brain Stimulation device implanted. People with Parkinson's disease often have issues related to sleep such as bad quality of sleep, waking up often and sleep apnea (breathing stops and starts during sleep). For this study, participants will be sleeping overnight in the study sleep lab for two nights. One night, Deep Brain Stimulation (DBS) device turned on and one night with the DBS off, either in this order or the reverse.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
6 Apr 2026
Start date
27 Feb 2026
Primary completion date
1 Feb 2028
Lead sponsor
The University of Texas Health Science Center at San Antonio
NCT number
NCT07636720

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 27 Feb 2026 to the primary completion date, 1 Feb 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Report dopaminergic medication changes in the past month.

Other illness

  • History of severe cardiovascular disease, untreated obstructive sleep apnea (OSA).
  • History of other neurological disorders affecting the central nervous system such as stroke, multiple sclerosis, tumors, amyotrophic lateral sclerosis or muscle disease such as muscular dystrophy, myopathy.
  • History of Dementia.

Who the study is looking for

  • Ability of subject to understand and the willingness to sign a written informed consent document.
  • Males and females; Age 40-80
  • Subjects with the diagnosis of idiopathic PD consistent with the United Kingdom Parkinson Disease society brain bank criteria, or documented diagnosis of Parkinson Disease who have a Deep Brain Implant, Percept RC device to subthalamic nucleus (STN) or Globus pallidus internus (GPi).
  • Willingness to adhere to the PSG regimen and turn DBS off for one night.
  • A score of ≥23 on the Montreal Cognitive Assessment (MoCA)
  • Be willing to stop any sleep hypnotics such as benzodiazepines and Ambien, with a 3 day washout period.

Age in the registry: 40 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The University of Texas Health Science Center at San Antonio - Brain Health Center
Coordinator of this site? Confirm its status
San AntonioUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.