University of Virginia
Charlottesville, Virginia, 22908, United States
Location status: Recruiting
NCT Number: NCT05565833
This randomized controlled trial will evaluate the impact of an Internet-delivered cognitive behavioral therapy for insomnia (CBT-I) intervention on sleep and the extent to which it contributes to cognitive health in individuals with mild cognitive impairment. Participants with insomnia who meet the study criteria for mild cognitive impairment will be recruited to determine the effects of the CBT-I intervention compared to a patient education condition on sleep and cognition. Internet-based recruitment methods will be used, and outcomes include sleep variables, daytime variables, and cognitive status.
Interested in participating?
Request Info65 year and older
All sexes
Interventional
Phase 2
Charlottesville, Virginia, 22908, United States
Location status: Recruiting
This randomized controlled trial will evaluate the impact of an Internet-delivered cognitive behavioral therapy for insomnia (CBT-I) intervention on sleep and the extent to which it contributes to cognitive health in individuals with mild cognitive impairment. Participants with insomnia who meet the study criteria for mild cognitive impairment will be recruited to determine the effects of the CBT-I intervention compared to patient education (PE) control condition on sleep and cognition. Internet-based recruitment methods will be used, and outcomes include sleep variables (reduced overall insomnia severity and wake after sleep onset), daytime variables (reduced levels of fatigue, improved quality of life, and improved mood), and cognitive status (memory, attention/psychomotor speed, and executive functioning domains). Participants will complete a pre-assessment battery, which consists of an online cognitive test, an online questionnaire, and two weeks of sleep diaries. Once complete, participants will be randomized to either the Internet-based PE or CBT-I intervention. At the start of week nine, all participants will be instructed to complete the post-assessment battery (cognitive test, questionnaires, and diaries). After completing the post-assessment, participants will have continued access to their assigned online program throughout the study duration. This same assessment (cognitive test, questionnaires, and diaries) will be completed at 6, 12, 18, and 24 months.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Cognitive Behavioral Therapy for insomnia delivered online and metered out over 6-9 weeks in a fully automated, interactive, tailored web-based program
An educational website containing information on insomnia
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Change in overall insomnia severity
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Change in periods of wakefulness occurring after defined sleep onset as measured by daily sleep diaries over 10-14 day periods, measured in minutes, collected through sleep diary entries
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Change in length of time that it takes to transition from wakefulness to sleep, measured in minutes, collected through sleep diary entries
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Change in self-report measures of five dimensions of fatigue ( general fatigue, physical fatigue, emotional fatigue, mental fatigue, and vigor) measured using Multidimensional Fatigue Symptoms Inventory-Short Form. Total MFSI-SF scores range from 24 to 96, with a higher score indicating a higher fatigue level
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
The SF-12 Health Survey will be used to measure changes in physical and mental quality of life. Scores range from 0 to 100, with higher scores indicating better physical and mental health
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Changes in attention and processing speed will be measured using the Cambridge Neuropsychological Test Automated Battery (CANTAB) Match to Sample Visual Search
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Changes in working memory and executive function will be measured using the Cambridge Neuropsychological Test Automated Battery (CANTAB) Spatial Working Memory Test
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Changes in episodic memory will be measured using the Cambridge Neuropsychological Test Automated Battery (CANTAB) Paired Associates Learning
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Amount of time spent asleep divided by the total time in bed
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Sleep knowledge and cognitive behavioral therapy for insomnia techniques; scores range from 0-10 and higher scores indicate greater insomnia knowledge
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Depression and anxiety are measured using the Center for Epidemiologic Studies Depression Scale (CES-D). Scores range from 0-60, where higher scores indicate greater likelihood of depression
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Falls questionnaire including number and frequency of falls
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Pain intensity and interference are measured using PROMIS Pain Intensity questions. On a scale of 0-100, a score of 50 is considered the mean/reference population, and higher scores indicate greater pain intensity.
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Global-, task-, and self-regulation self-efficacy changes are measured using Self-Efficacy Scale developed by Bouchard, Bastien & Morin (2010) and includes 40 questions. Questions are answered using a scale from 0 (can't do at all) to 100 (absolutely certain can do), where higher scores indicate higher self-efficacy.
Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months
Activities that allow an individual to live independently in a community. Score range from 0 (low function, dependent) to 8 (high function, independent).
Contact information is provided by the study sponsor or research team.
University of Virginia
Other
Internet-based Insomnia Intervention to Prevent Cognitive Decline in Older Adults With Mild Cognitive Impairment (SHUTi MIND)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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