Feasibility of Continuous Sleep Recording in Patients Undergoing Deep Brain Stimulation for Parkinson's Disease

Fondation Ophtalmologique Adolphe de Rothschild5 enrolled

Overview

This pilot study aims to assess a new device designed for an objective measure of sleep parameters. The purpose of the device is to assess, in a more simple and precise way, the impact of deep brain stimulation on patient's sleep.

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Parkinson Disease

Interventions

Sleep RecordingDEVICE

the device records movements during patients' sleep

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * patient \> 18 years old * with Parkinson disease * scheduled for implantation of electrodes for deep brain stimulation Exclusion criteria: * pregnant or breast feeding patient * refusal to participate in the study * patient under legal protection * no health insurance coverage

Outcomes

Primary Outcomes

mean sleep duration per night

Time frame: 15 days

mean sleep onset latency

Time frame: 15 days

mean number of awakenings per night

Time frame: 15 days

Data from ClinicalTrials.gov

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