Could a little less oxygen sharpen your memory? new trial explores a surprising therapy for mild cognitive impairment.
NCT ID NCT05495087
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether short sessions of breathing air with slightly less oxygen (intermittent hypoxia training) can safely improve memory and thinking in adults aged 55-79 with mild cognitive impairment. Participants will be assigned to either the real treatment or a sham (fake) version for up to 12 weeks. The goal is to see if this simple, non-drug approach can boost brain function and even increase brain volume.
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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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About 66 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2023
- Expected to finish
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Apr 2026
An estimate. End dates often move.
- 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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55 to 79 years
- 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: * Adult men and women ages 55 to 79 years old who have been diagnosed with MCI. * Must be willing to be assigned to either group: treatment or sham-treatment control. * Able to pay multiple visits to the lab for the proposed assessments. * Able to breathe moderately hypoxic air via an air-cushioned, disposable facemask. * To have controlled stabilized chronic conditions of at least 6 months duration, such as hypertension, coronary artery disease, diabetes or metabolic disease, chronic bronchitis, degenerative osteoporosis or arthritis and/or other aging-related chronic conditions. * Must be depression-free at the time of enrollment. * Must have arterial oxygen saturation at or above 95% and cerebral tissue oxygenation at or above 50% at rest. * Woman subject must be post-menopausal. Exclusion Criteria: * Unwilling to sign a written consent to participate in this double-blinded placebo-controlled phase I trial. * Diagnosed with AD-dementia or have impaired independent daily functioning; with MMSE \<20 and/or CDR ≥1. * Unable to visit the lab independently. * Claustrophobic to facemask and hyper-reactive to hypoxia exposure. * Expecting any major surgery or transplant. * Have un-controlled chronic conditions including systolic-diastolic pressures over 150/90 mmHg with medications, diabetes, chronic renal failure (based on the medical history questionnaire), recurrent chest pain, seizures or epilepsies, moderate to severe carotid stenosis or calcification, brain aneurysm, uncontrolled allergic rhinitis, pulmonary fibrosis, emphysema, cancer, infectious disease, atrial fibrillation, regular pre-mature ventricular contractions, myocardial ischemia or infarct, 2nd or 3rd degree atrio-ventricular blockade. * Have severe head injury or traumatic brain injury, stroke (hemorrhagic and/or ischemic). * Have currently diagnosed depression. * Currently have COVID-19. * Have any metallic implants or who are claustrophobic. * Currently participating in any interventional study and/or have been previously exposed to hypoxia, such as residing more than two months at altitudes above 5000 ft. within the past 3 years or previously participated in a hypoxia training study.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of North Texas Health Science Center
RECRUITINGFort Worth, Texas, 76107, United States
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