Sleep Apnea in Multiple Sclerosis Positive Airway Pressure Trial

McGill University49 enrolled

Overview

Fatigue is highly prevalent among multiple sclerosis (MS) patients and has pervasive adverse effects on daily functioning and quality of life. The investigators found in a recent study that obstructive sleep apnea-hypopnea (OSAH) is the most common sleep abnormality in multiple sclerosis (MS) patients. There was also a significant relationship between OSAH and higher fatigue scores in MS patients. Preliminary work from the investigators in this group of subjects shows that treatment of sleep disorders (mostly OSAH) can improve fatigue and other symptoms in some MS patients. However, it is now necessary to systemically test the effect of OSAH treatment in a randomized, controlled study, to be sure that it really does improve fatigue and other symptoms. The best treatment for OSAH in the general population is continuous positive airway pressure (CPAP). This treatment has been well tolerated by most MS patients who have used the device at the investigators' center. This project will therefore be a randomized, controlled, clinical trial of CPAP in MS patients with OSAH. The effects of six months of CPAP treatment on fatigue as well as sleep quality, somnolence, pain, disability, and quality of life will be studied.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Obstructive Sleep Apnea-hypopnea in Multiple Sclerosis Patients

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Diagnosis of multiple sclerosis by a neurologist based on standard criteria (Annals Neurol 2011; 69:292-302) * Expanded Disability Status Scale score of 0 to 7.0 * MS-relapse free for \>30 days prior to screening * Pittsburgh sleep quality Index \> 5 * Fatigue Severity Scale score \>=4 * Montreal Cognitive Assessment (MoCA) \>= 26 * diagnosis of OSAH by polysomnography showing AHI \>= 15 events/h of sleep * forced vital capacity \>60% predicted Exclusion Criteria: * pregnancy or planned pregnancy * psychiatric conditions which could preclude compliance with informed consent, study procedures, or study requirements * other significant neurological, pulmonary, otorhinological, and medical disorders * major depression within the past year * any value of \>1.5 times the upper limit or \<0.75 the lower limit of the reference range for any standard clinical hemogram and biochemistry determinations which is clinically significant * current treatment for OSAH * presence of another untreated sleep disorder which is clinically significant * very severe OSAH (safety criterion)defined as an AHI \>30 with either a 4% O2 desaturation index \>15 events/h OR work in a safety-critical position OR an ESS score \>=15

Outcomes

Primary Outcomes

Fatigue Severity Scale

Time frame: Six months