No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
60 – 85
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
80 (estimated)
Sponsor
Darren P Casey · Other
Who this trial is looking for
This trial is looking for older adults, with and without type 2 diabetes, to see if a treatment called intermittent hypoxia can help improve brain health. Participants will need to meet certain health criteria and complete some tests.
Are You a Good Fit for This Trial?
Rules you outType 1 diabetes
You may be able to join if
I am between 60 and 85 years old.
I score 26 or higher on the MoCA test.
I have been diagnosed with type 2 diabetes.
You may not be able to join if
I was diagnosed with diabetes less than 1 year ago.
I have had a heart attack or stroke in the last year.
I have uncontrolled hypertension.
I have obstructive sleep apnea.
I have dementia.
I have kidney problems with an eGFR less than 60 ml/min.
I have a body mass index over 40 kg/m2.
I smoke or have smoked in the past year.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The purpose of this study is to use a randomized, placebo-controlled study design to rigorously examine the therapeutic potential of intermittent hypoxia (IH) for improving cerebrovascular health in older adults with and without type 2 diabetes mellitus (T2DM).
Trial Locations
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Eligibility Criteria
For 30 patients with documented Type 2 diabetes
Inclusion Criteria:
* Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures.
* Age is \> or = 60 and \< or = 85 years of age
* Documented Type 2 dia…
For 30 patients with documented Type 2 diabetes
Inclusion Criteria:
* Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures.
* Age is \> or = 60 and \< or = 85 years of age
* Documented Type 2 diabetes
* Scoring 26 or higher on the MoCA test
Exclusion criteria:
* diagnosis of type 2 diabetes \< 1 year prior to enrollment
* HbA1c \<6.5% or \>10.0%
* body mass index \> 40 kg/m 2
* incident cardiovascular events in the last year (heart attack, stroke)
* symptomatic coronary artery disease and/or heart failure
* uncontrolled hypertension
* obstructive sleep apnea
* pulmonary disease
* dementia
* renal impairment with creatinine clearance (eGFR) of \<60 ml/min
* smoking or history of smoking within past one year
30 nondiabetic control subjects will also be studied.
Inclusion criteria:
* Willing and able to provide written, signed informed consent after the nature of the study has been explained, and prior to any research-related procedures.
* Age is \> or = 60 and \< or = 85 years of age
* Scoring 26 or higher on the MoCA test
Exclusion criteria:
* Diagnosis of diabetes (Type 1 or Type 2)
* body mass index \> 40 kg/m2
* incident cardiovascular events in the last year (heart attack, stroke)
* symptomatic coronary artery disease and/or heart failure
* uncontrolled hypertension
* obstructive sleep apnea
* pulmonary disease
* dementia
* renal impairment with creatinine clearance (eGFR) of \<60 ml/min
* smoking or history of smoking within past one year
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