Could treating sleep apnea help prevent Alzheimer's? new study investigates
NCT ID NCT05094271
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This completed Phase 1 study looked at whether obstructive sleep apnea (OSA) might contribute to Alzheimer's disease. Researchers studied 182 older adults aged 65-85 with and without OSA, using brain scans and breathing tests. The goal was to understand how sleep disruptions like apnea could affect Alzheimer's-related brain changes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Supplemental oxygen and continuous positive airway pressure (CPAP) machine
- What this could lead to
- If successful, this study could help clarify whether treating sleep apnea might slow or prevent Alzheimer's disease.
- What could go wrong
- This is an early, completed study focused on understanding the link, not testing a treatment. Results may not lead to direct clinical changes.
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
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
182 people
The number who actually took part.
- Started
-
Oct 2021
- Finished
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Jun 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
-
65 to 85 years
- Sex
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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: 1. Age 65-85 years 2. Gender: Men or Women 3. MOCA \> 26 4. Independently living and able to drive 5. OSA (AHI ≥ 15/h) or no OSA 6. Subjects must consent to waiving their right to obtain their PHS score (since the score is not yet actionable and could lead to social stress and ethical dilemmas) Exclusion Criteria: 1. Currently smoking 2. History of COPD or asthma 3. Heart Failure Class III or IV, unstable cardiovascular disease, or uncontrolled hypertension 4. Neuromuscular Disease 5. Drowsy Driving (ESS \> 18/24) 6. Inability to complete study procedures, such as questionnaire that are only available/validated in English 7. Lack of decisional capacity to provide informed consent 8. Participants in whom magnetic resonance imaging Magnetic Resonance Imaging \[MRI\] is contraindicated including, but not limited to, those with a pacemaker, presence of metallic fragments near the eyes or spinal cord, or cochlear implant 9. Presence of a brain tumor or lobar stroke 10. Current drug or alcohol abuse/dependence 11. Prisoners
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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
-
UCSD Sleep Research
La Jolla, California, 92037, United States
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