Buying Time: Improving Sleep to Promote Cognitive Function in Older Adults
NCT ID: NCT02926157
Last Updated: 2019-05-09
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
96 participants
INTERVENTIONAL
2016-10-31
2018-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Life Style and Sleep Group
Participants randomized into this group will undergo a 4 week sleep hygiene course (classes 1x/week for 1.5 hours), followed by a 20 week lifestyle activation program. During the 20 week lifestyle activation program, participants wear a Fit Bit and receive a call from a fitness professional every other week for motivation and recommendations, and receive a bright light therapy program from a sleep expert based on their initial sleep results at the baseline measurement session.
Life Style and Sleep Intervention
Wait-list Control
Participants randomized into this group will complete all measurement sessions. After completion of the final measurement session (6 months), participants will be offered an abbreviated version of the Life Style and Sleep Group intervention including the sleep hygiene course, consultation with sleep expert to go over individual sleep patterns and be given recommendations, along with physical activity recommendations from a fitness expert.
No interventions assigned to this group
Interventions
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Life Style and Sleep Intervention
Eligibility Criteria
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Inclusion Criteria
* Community-dwelling (not in a long term care facility)
* Read, write, and speak English
* Able to walk independently
* In sufficient health to participate in regular physical activity
Exclusion Criteria
* Receiving continuous positive air pressure (CPAP) treatment
* Diagnosed with dementia of any type
* At high risk for cardiac complications during physical activity or unable to self-regulate activity or understand recommended activity level
* Have a clinically important peripheral neuropathy or sever musculoskeletal or joint disease that impairs mobility
65 Years
85 Years
ALL
No
Sponsors
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University of British Columbia
OTHER
Responsible Party
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Teresa Liu-Ambrose
Principal Investigator
Principal Investigators
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Teresa Liu-Ambrose, PhD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Glenn Landry, PhD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Linda Li, PhD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Catherine Chan, MPT
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
John Best, PhD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Cindy Barha, PhD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Jennifer Davis, PhD
Role: PRINCIPAL_INVESTIGATOR
University of British Columbia
Locations
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University of British Columbia
Vancouver, British Columbia, Canada
Countries
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References
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Balbim GM, Boa Sorte Silva NC, Falck RS, Kramer AF, Voss MW, Liu-Ambrose T. 24-hour activity cycle behaviors and gray matter volume in mild cognitive impairment. Alzheimers Dement. 2025 Jul;21(7):e70496. doi: 10.1002/alz.70496.
Falck RS, Davis JC, Best JR, Chan PCY, Li LC, Wyrough AB, Bennett KJ, Backhouse D, Liu-Ambrose T. Effect of a Multimodal Lifestyle Intervention on Sleep and Cognitive Function in Older Adults with Probable Mild Cognitive Impairment and Poor Sleep: A Randomized Clinical Trial. J Alzheimers Dis. 2020;76(1):179-193. doi: 10.3233/JAD-200383.
Falck RS, Davis JC, Best JR, Li LC, Chan PCY, Wyrough AB, Landry GJ, Liu-Ambrose T. Buying time: a proof-of-concept randomized controlled trial to improve sleep quality and cognitive function among older adults with mild cognitive impairment. Trials. 2018 Aug 17;19(1):445. doi: 10.1186/s13063-018-2837-7.
Other Identifiers
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H16-01029
Identifier Type: -
Identifier Source: org_study_id
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