Alzheimer's sleep breakthrough? tiny study tests citicoline
NCT ID NCT05200208
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This pilot study tested whether a dietary supplement called citicoline could improve sleep and cognitive function in 20 people with Alzheimer's disease. Participants took either citicoline or a placebo for 3 months, and researchers measured sleep quality, daytime sleepiness, and thinking skills. The goal was to see if this well-tolerated supplement might ease common sleep problems in Alzheimer's and potentially boost memory and attention.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- citicoline (dietary supplement)
- What this could lead to
- If it works, this could point toward a simple supplement to help Alzheimer's patients sleep better and think more clearly.
- What could go wrong
- This is a very small pilot study with only 20 people, so results may not apply to everyone. It's also too early to know if citicoline truly helps.
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
-
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
-
20 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Sep 2025
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Participants who are diagnosed with AD and confirmed from the medical record. * At least 18 years of age living within the continental United States * Read and understand English * Have Internet and email access (this criterion applies to the legally authorized representatives) Exclusion Criteria: * No telephone access * Epilepsy or head trauma resulting in unconsciousness in the past two years * Presence of chronic obstructive pulmonary disease, asthma, severe cardiac insufficiency (congestive heart failure, myocardial infarction), type I diabetes, vitamin B12 or folic acid deficiency, liver cirrhosis, thyroid dysfunction, rheumatoid arthritis, chronic renal failure, and/or psychiatric disorders, obstructive sleep apnea, restless legs syndrome or periodic limb movement disorder * History of alcohol dependence and medication abuse * Night shift workers or those in situations where they regularly experience jet lag, or have irregular work schedules, since circadian misalignment may alter markers of inflammation
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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
-
Emory University School of Nursing
Atlanta, Georgia, 30322, United States
-
Goizueta Alzheimer's Disease Research Center
Atlanta, Georgia, 30329, United States
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