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Sleep Disordered Breathing and Its Impact on Neuro-cognitive Performance and Quality of Life in Parkinson Disease

Sleep Disordered Breathing and Its Impact on Neuro-cognitive Performance and Quality of Life in Parkinson Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02034357
Enrollment
89
Registered
2014-01-13
Start date
2011-06-30
Completion date
2016-03-31
Last updated
2016-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's Disease, Sleep Disordered Breathing, Sleep Obstructive Apnea

Keywords

Parkinson Disease, Sleep Disordered Breathing, Sleep Obstructive Apnea, Polysomnography, CPAP (continuous positive airway pressure) titration, CPAP (continuous positive airway pressure) treatment

Brief summary

The purpose of this study is to determine the impact of sleep and breathing problems during sleep on memory, attention, and general well being (quality of life) in people with Parkinson Disease.

Detailed description

During the 2 year award period, we will prospectively enroll 200 patients with idiopathic Parkinson Disease (PD), who meet eligibility criteria below. All patients will undergo a baseline polysomnography (PSG) to diagnose Sleep Disordered Breathing (SDB) and will be asked to complete validated questionnaires to measure Sleep Quality, SDB risk, insomnia severity, daytime sleepiness, presence of restless leg syndrome (RLS), anxiety/depression, and quality of life. Medical records will be reviewed to determine co-morbidities and medication use. Each PD participant will undergo a full neurological examination, including the Unified Parkinson's Disease Rating Scale (UPDRS), the Hoehn & Yahr stage and a battery of neuro-cognitive measures at baseline. Patients with SDB will be offered PAP titration and treatment for 4 months. All patients (SDB \[PAP compliant, non-compliant\], and no SDB \[controls\]) will complete repeat neuro-cognitive evaluation, questionnaires, neurological evaluation and UPDRS assessment at 4 month and at 1 year follow-up. PD participants will be assessed in the on state in the morning. In the event that a participant goes off during testing, a break will be taken and participants will be given the option of taking their medication to return to the on state and resume testing or they can return later in the week to complete the evaluation. Although participants will understand the general purpose of the study, they will be blinded to the major study hypothesis. Neuropsychological examiners and the neurologist conducting the neurological exam will be blinded to the SDB status of the patient. Four month follow-up will be staggered according to enrolment date and will be completed by Year 2.

Interventions

OTHERNeurocognitive function

Each eligible participant will complete a neuro-cognitive assessment as measured by CVLT at the beginning of the study. Neurocognitive evaluations will be repeated at 4-month and 1-year follow-up.

OTHERSleep evaluations

Each eligible participant will complete sleep questionnaires and undergo a baseline sleep study at the beginning of the study. The sleep questionnaires will be repeated at 4-month and 1-year follow-up.

Sponsors

National Parkinson Foundation
CollaboratorOTHER
University of Miami
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Able to give consent. * ≥18 years and have a Hoehn and Yahr stage at the time of enrollment of ≤3, clinical diagnosis of idiopathic Parkinson's Disease meeting the United Kingdom Parkinson's Disease Society Brain Bank criteria. * Stable medical condition, including medications in the 1 month prior to enrollment.

Exclusion criteria

* Previous diagnosis of SDB with active use of Positive Airway Pressure (PAP), surgery for SDB or tracheostomy. * Inability to read and comprehend English and/or Spanish at a grade 5 level. * Prior history of neurosurgical procedures for PD or any other condition. * Diagnosis of dementia as defined by Mini-mental state examination (MMSE) of \< 26. * History of major uncontrolled psychiatric illness. * History of drug or alcohol abuse/dependence. * History of major head injury or other neurological disease. * Patients with observable craniofacial abnormalities that may be a relative contraindication to PAP.

Design outcomes

Primary

MeasureTime frameDescription
Changes from Baseline Neurocognitive function in Parkinson's disease patients at 4 month and 1 year follow-up as measured by California Verbal Learning Test (CVLT)Baseline, week 4, year 1Changes from Baseline Neurocognitive function (verbal learning and memory) in Parkinson's disease patients at 4 month and 1 year follow-up as measured by California Verbal Learning Test (CVLT).

Secondary

MeasureTime frameDescription
Prevalence of Sleep Disordered Breathing (SDB) in a diverse cohort of idiopathic PD patients.BaselineDetermine the Prevalence of Sleep Disordered Breathing (SDB) in a diverse cohort of idiopathic PD patients.
Prevalence of Insomnia in a diverse cohort of idiopathic PD patients.BaselinePrevalence of Insomnia in a diverse cohort of idiopathic PD patients.
Prevalence of Poor Sleep Quality in a diverse cohort of idiopathic PD patients.BaselinePrevalence of Poor Sleep Quality in a diverse cohort of idiopathic PD patients.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026