Use of an Internet-Based Insomnia Intervention to Prevent Cognitive Decline in Adults With Mild Cognitive Impairment (SHUTi OASIS)
Mild Cognitive Impairment, Cognitive Impairment, Insomnia
About this trial
This is an interventional other trial for Mild Cognitive Impairment
Eligibility Criteria
Inclusion Criteria:
55 years of age or older
- ability to read and speak English
- US resident
- MCI diagnosis or scores within acceptable range on R-BANS assessment.
- regular access to Internet and Email
- willingness to use Internet and Email
- ability to use a computer
- no more than 6.5 hours of sleep per night
- the sleep disturbance (or associated daytime fatigue) must cause significant distress or impairment in social, occupational, or other areas of functioning over past 3 months
- sleep onset latency > 30 minutes at least 3x/week for past three months; OR wake after sleep onset >30 minutes at least 3x/week for past three months
Participants on stable (defined as no change in the past 3 months) medication regimens will be eligible including sleep medications, unless the medication is known to cause insomnia (e.g., steroids).
Exclusion Criteria:
bedtime outside of 8pm-2am and arise times outside of 4-10am
- current psychological treatment for insomnia
- initiation of psychological or psychiatric treatment within past 3 months
- current severe/very severe depression from QIDS-C16
- current moderate/high risk suicide or substance use disorder in 12 months from MINI
- other untreated sleep disorders (e.g., obstructive sleep apnea, restless legs syndrome)
- current diagnosis of Huntington's or Parkinson's disease
- current treatment for hyperthyroidism
- currently undergoing chemotherapy
- presence of asthma or respiratory concerns with night treatment
- chronic pain treated with opioids
- epilepsy
- inability to provide informed consent
- Not concurrently enrolled in any other intervention or educational study targeting sleep.
Sites / Locations
- University Of Virginia
Arms of the Study
Arm 1
Other
Internet-Based Insomnia Intervention
2 weeks of online sleep diaries. Participants will also wear an Actiwatch at night, which records measurements of movements of a limb, providing an estimation of sleep duration, sleep pattern and disturbed sleep. 9 week interveition period, subjects complete the internet based CBT-I program, consisting of six Cores (Getting Ready, Sleep Scheduling, Sleep Practices, Thinking Differently, Sleep Hygiene, and Moving On).Each Core takes approximately 45-60 minutes to review online, and most participants spend an additional 30-45 minutes per week on recommended exercises. Participant will then be instructed to complete a post-Assessment, consisting of one online questionnaire and two weeks of Daily Sleep Diaries. The Actiwatch is worn as before during this two week period.