Cognitive Behavioral Therapy for Insomnia for the Dementia Caregiving Dyad
NCT ID: NCT04426838
Last Updated: 2023-03-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
44 participants
INTERVENTIONAL
2020-09-30
2023-03-10
Brief Summary
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Detailed Description
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Cognitive behavioral therapy for insomnia (CBTi), a non-pharmacologic intervention that has demonstrated effectiveness for improving sleep disturbances in multiple populations, is delivered in various formats including face-to-face and videoconferencing. Individually, PLwD and caregivers have successfully deployed behavioral sleep techniques, resulting in improved sleep quality. However, there is no current published research on CBTi completed simultaneously by the PLwD-caregiver dyad, and that is exactly what the researchers of this study seek to do with early-stage individuals and their caregivers. The researchers premise this effort on the notion that a dyadic intervention can use early-stage individuals' retained capacity for communication and comprehension to establish in-the-moment agreements about strategies the caregiver can employ to enact and facilitate positive sleep behaviors in the PLwD and to pair that with acquired strategies to engender his/her own positive sleep behaviors.
This project seeks to gather formative and preliminary data on CBTi delivered simultaneously to the PLwD-caregiver dyad. The researchers will use a quantitative, descriptive approach to determine the feasibility, acceptability, and preliminary efficacy of a 4-session CBTi intervention administered to 40 PLwD-caregiver dyads via videoconferencing sessions who will receive the intervention as a unit. Objective and subjective sleep, depressive symptoms, and cognitive health data will be collected at baseline, and 1 week and 3 months post-completion of the intervention.
In community-dwelling PLwD and their caregivers where both persons in the dyad self-report sleep disturbances, the specific aims for this study are:
1. Assess the feasibility of a video conferencing dyad-based CBTi intervention.
2. Evaluate the acceptability of a video conferencing dyad-based CBTi intervention.
3. Examine the preliminary efficacy of video conferencing CBTi intervention on sleep quality outcomes including sleep efficiency and perceived sleep quality.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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PLwD Cognitive Behavioral Therapy for Insomnia (CBTi)
Persons living with dementia in a dyad receiving the CBTi intervention in a videoconferencing format.
Cognitive Behavioral Therapy for Insomnia (CBTi) via Videoconference
The CBTi protocol will include stimulus control, sleep compression, relaxation, sleep hygiene, and cognitive restructuring which will be done over 4 weeks with one session weekly delivered via videoconference.
Caregiver Cognitive Behavioral Therapy for Insomnia (CBTi)
Caregivers in a dyad receiving the CBTi intervention in a videoconferencing format.
Cognitive Behavioral Therapy for Insomnia (CBTi) via Videoconference
The CBTi protocol will include stimulus control, sleep compression, relaxation, sleep hygiene, and cognitive restructuring which will be done over 4 weeks with one session weekly delivered via videoconference.
Interventions
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Cognitive Behavioral Therapy for Insomnia (CBTi) via Videoconference
The CBTi protocol will include stimulus control, sleep compression, relaxation, sleep hygiene, and cognitive restructuring which will be done over 4 weeks with one session weekly delivered via videoconference.
Eligibility Criteria
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Inclusion Criteria
* Co-residence with the caregiver in the community
* Montreal Cognitive Assessment (MOCA) score between 12 and 25
* Stable dose of psychotropic medications, anti-dementia, sedatives/hypnotics, or opioids in the past 90 days
* Presence of sleep problems determined by using the proxy-rated Sleep Disorders Inventory (presence of at least one sleep disturbance symptom of moderate severity)
* Informal caregivers (family/friends) of co-residing PLwD
* Providing unpaid assistance, on average 20 hours weekly, for a person in the early stage of illness who is community-dwelling
* Presence of sleep problems: sleep onset latency or wake after sleep onset more than 30 minutes more than 3 nights weekly
* Tolerate and agrees to wear wrist actigraph
* Be able to read, speak and understand English
* Have no uncorrectable vision or hearing deficits that might impede participation
Exclusion Criteria
* Moderate to severe cognitive impairment defined as MoCA score \<17
* Current sedative-hypnotic or other sleep aid use on a regular or as needed schedule within the prior three months
* Presence of an acute medical or psychiatric condition which would interfere with the subject's ability to realistically follow the study protocol
18 Years
ALL
Yes
Sponsors
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Alzheimer's Association
OTHER
Emory University
OTHER
Responsible Party
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Glenna Brewster
Assistant Professor
Principal Investigators
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Glenna Brewster, PhD, RN
Role: PRINCIPAL_INVESTIGATOR
Emory University
Locations
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Emory University
Atlanta, Georgia, United States
Goizueta Alzheimer's Disease Research Center
Atlanta, Georgia, United States
Countries
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Other Identifiers
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IRB00115210
Identifier Type: -
Identifier Source: org_study_id
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