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NCT07173543Recruiting

IH, Brain Health, and T2D

Intermittent Hypoxia Training and Cerebrovascular Health in Older Adults With Type 2 Diabetes

Source: ClinicalTrials.gov · Last updated 13 Mar 2026

Brief summary (registry, in English)

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).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
80 (estimated)
First submitted
2 Sept 2025
Start date
22 Sept 2025
Primary completion date
30 Jun 2028
Lead sponsor
Darren P Casey
NCT number
NCT07173543

What you commit to

  • Study type: Interventional
  • Planned participants: 80
  • From 22 Sept 2025 to the primary completion date, 30 Jun 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • diagnosis of type 2 diabetes \< 1 year prior to enrollment

Other illness

  • incident cardiovascular events in the last year (heart attack, stroke)
  • symptomatic coronary artery disease and/or heart failure
  • uncontrolled hypertension
  • pulmonary disease
  • dementia
  • smoking or history of smoking within past one year
    • 30 nondiabetic control subjects will also be studied.
  • Diagnosis of diabetes (Type 1 or Type 2)
  • incident cardiovascular events in the last year (heart attack, stroke)
  • symptomatic coronary artery disease and/or heart failure
  • uncontrolled hypertension
  • pulmonary disease
  • dementia
  • smoking or history of smoking within past one year

Lab values

  • HbA1c \<6.5% or \>10.0%
  • renal impairment with creatinine clearance (eGFR) of \<60 ml/min
  • renal impairment with creatinine clearance (eGFR) of \<60 ml/min

Other

  • body mass index \> 40 kg/m 2
  • obstructive sleep apnea
  • body mass index \> 40 kg/m2
  • obstructive sleep apnea

Who the study is looking for

  • 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
  • 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

Criteria the registry did not label

  • For 30 patients with documented Type 2 diabetes

Age in the registry: 60 years to 85 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Iowa
Coordinator of this site? Confirm its status
Iowa CityUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.