A Sleep Program to Improve Sleep Quality in People With HIV
HIV - Human Immunodeficiency Virus, Insomnia Disorder
About this trial
This is an interventional diagnostic trial for HIV - Human Immunodeficiency Virus focused on measuring HIV - Human Immunodeficiency Virus, digital cognitive behavioural therapy for insomnia (dCBT-I), insomnia, cognitive Impairment, concentration, productivity
Eligibility Criteria
Inclusion Criteria:
- Evidence of insomnia disorder (Sleep Condition Indicator [SCI] ≤ 16)
- Able to have convenient weekly access to the Internet
- Stable medical condition
- Have been on a stable HAART regimen for > 6 months
- Have not had a change in medications that could potentially interfere with sleep or cognition in the past 4 months.
Exclusion Criteria:
- Berlin questionnaire score indicating high risk of obstructive sleep apnea
- Known history of sleep disorders (e.g., narcolepsy, hypersomnia, restless legs syndrome, REM-sleep behavior disorder) which currently require or previously required treatment
- Ongoing involvement in night shift work
- Not able to complete the 12 weeks of the sleep intervention due to a scheduling conflict
Sites / Locations
- Montreal Neurological Institute and Hospital (McGill University)
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Immediate dCBT-I group
Waitlist control group
Digital cognitive behavioural therapy for insomnia (dCBT-I) is a 6 session training program (spanning 6 to 12 weeks) designed to improve sleep. Participants in the immediate dCBT-I group will receive the Sleepio intervention shortly after enrollment.
Participants in the waitlist control group will receive sleep hygiene recommendations from validated online resources for HIV patients (http://www.catie.ca/en/positiveside/winter-2013/sleep-tight) around the time of enrollment. They will start the digital cognitive behavioural therapy for insomnia (dCBT-I) intervention 12-14 weeks after the initial enrollment.