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Study identifier: NCT04632628 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Web-based Cognitive Behavioral Treatment for Insomnia in Dementia Caregivers

Condition: Insomnia Chronic · Dementia  ·  Sponsor: University of South Florida

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

Over the next 30 years, more than 10 million persons living with dementia in the United States will receive care at home from an unpaid and untrained family caregiver. At home care is preferred by caregivers and persons with dementia alike, but increases the caregiver's risk of insomnia and related negative health outcomes, including depression, anxiety, cognitive disturbances and poor quality of life. Cognitive behavioral therapy for insomnia (CBT-I) is a highly effective and established evidence based treatment for adults of all ages. Although relatively understudied in dementia caregivers, the research by our group and others suggests CBT-I is also efficacious in caregivers. Our team developed a brief (4 session) CBT-I protocol specifically adapted for dementia caregivers (CBT-I) and has shown in person and remote (i.e. telehealth) delivery of this protocol significantly reduces insomnia symptoms and improves mood (moderate to large effects). Given demands on caregivers' time and limited availability of trained CBT-I providers, a web-based version of CBT-I (WebCBT-I; the online treatment will be called NiteCAPP) is needed to increase the accessibility of this efficacious treatment. WebCBT-I will allow for flexible at home scheduling, and the skills needed to monitor caregiver treatment progress can be quickly and efficiently taught to healthcare providers. The overarching goal of this project is to develop and test WebCBT-I in caregivers of persons with dementia. Objectiv…

This description comes directly from the study's public registry record.

Talk to the study team

Christina S McCrae  ·  573-882-0982  ·  mccraec@health.missouri.edu

Riley Stephens  ·  573-882-8881  ·  rstephens@health.missouri.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of MissouriColumbia, Missouri, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT04632628