Sleep therapy tested for Alzheimer's brain fog
NCT ID NCT03256539
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a behavioral program using bright light therapy and sleep coaching to improve sleep and thinking in older adults with mild cognitive impairment or mild Alzheimer's. Only 15 people were enrolled before the study was stopped early. The goal was to see if the program was feasible and could help with memory and daily function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- behavioral sleep intervention (bright light therapy and modified cognitive behavioral therapy for insomnia)
- What this could lead to
- If successful, this could point toward a non-drug way to improve sleep and thinking in people with early Alzheimer's.
- What could go wrong
- This was a very small pilot study (15 people) that was terminated early, so results are limited and may not apply to others.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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15 people
The number who actually took part.
- Started
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Aug 2021
- Finished
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Jan 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * ≥65 years old * Memory complaints verified by an informant * Clinical diagnosis of mild cognitive impairment (MCI) or mild Alzheimer's Disease * General cognitive performance sufficiently persevered such that a diagnosis of Alzheimer's disease cannot be made by the site physician * No evidence (CT or MRI scans within 12 months prior to screening) of infection, infarction, or other focal lesions and no clinical symptoms suggestive of intervening neurological disease * Adequate visual and auditory acuity to allow neuropsychological testing * Meets International Classification of Sleep Disorders-2nd edition (ICSD-2) criteria for insomnia or circadian rhythm disorders, or shows actigraphy evidence of sleep disturbances and excessive napping Exclusion Criteria: * Any major neurologic disease other than suspected incipient Alzheimer's disease, such as Parkinson's disease, multi-infarct dementia, multiple sclerosis, seizure disorder, Huntington's disease, brain tumor or history of significant head trauma * Any comorbid psychiatric conditions or severe personality disorder within the past 2 years (by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition), such as major depression, bipolar disorder, schizophrenia and other psychotic features * Any uncontrolled medical conditions or systemic illness that might lead to difficulty complying with the study protocol * History of alcohol or substance abuse within the past 2 years * Any inadequately treated primary or secondary sleep disorder (due to medical conditions) that might confound the association
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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UCSF
San Francisco, California, 94121, United States
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