A Pilot Study of CPAP Adherence Promotion by Peer Buddies With Sleep Apnea (CPAPPs)
Sleep Apnea
About this trial
This is an interventional treatment trial for Sleep Apnea focused on measuring sleep apnea, adherence
Eligibility Criteria
Inclusion Criteria:
- Obstructive Sleep Apnea (defined by Apnea-hypopnea index [AHI] > 5 per hour; with hypopneas defined as greater than 30% reduction in airflow with 4 or greater drop in oxygen saturation). AHI will be determined by full night or split-night polysomnography.
- Age range 21 - 85 years old.
- Stable medical history and no change in medications, including anti-hypertensive and thyroid replacement, in the previous 4 months.
- No regular use (> 3 times/week) of sedative or hypnotic medications in the last 4 months.
Exclusion Criteria:
- Central sleep apnea (central apnea index > 5 per hour and >50% of Apnea-hypopnea index constituted by central apneas and non-obstructive hypopneas).
- Complex sleep apnea or CPAP emergent central apnea (Central apnea index > 5 per hour during CPAP titration with >50% of Apnea-hypopnea index constituted by central apneas and non-obstructive hypopneas).
- Requiring oxygen or bi-level positive airway pressure for treatment of OSA or hypoventilation.
- Decompensated cardiac (heart failure or angina) or pulmonary (severe COPD or uncontrolled asthma) disease
- Chronic narcotic use
- Nasal obstruction (nasal congestion score > 15) or enlarged tonsils
- Diagnosis of another sleep disorder in addition to OSA based on PSG (e.g., periodic limb movement disorder [ 15 limb movements/hour of sleep with arousal], central sleep apnea [ 50% of apneas on diagnostic PSG are central apneas], insomnia, obesity hypoventilation syndrome, or narcolepsy).
- Previous treatment with positive airway pressure, home oxygen therapy, tracheotomy, uvulopalatopharyngoplasty, or other surgery for OSA.
- Night shift workers in situations or occupations where they regularly experience jet lag, or have irregular work schedules by history over the last 6 months.
- Routine consumption of more than 2 alcoholic beverages per day.
- Recent or recurring history of recreational drug use leading to tolerance or dependence.
- Unable to perform tests due to inability to communicate verbally, inability to write and read in English; less than a 5th grade reading level; visual, hearing or cognitive impairment (e.g. previous head injury); or upper extremity motor deficit (e.g., previous stroke that prevents patient from using CPAP treatment).
Sites / Locations
- Southern Arizona VA Health Care System, Tucson, AZ
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Arm 1
Arm 2
Trained peers with sleep apnea will be paired with the newly diagnosed patients over a 3-month period. During this time the trained peers will share experiences on coping strategies with CPAP device and equipment (promote self efficacy), share their positive experiences (motivational effects and outcome expectancies), share their knowledge of perceived vulnerabilities due to untreated sleep apnea (promote risk perception), share methods for improving efficacy of CPAP equipment and interface (patient education) and prepare their subjects for upcoming physician or respiratory therapist appointments (patient activation).
Usual care