Actively Recruiting

Phase Not Applicable
Age: 60Years - 85Years
All Genders
Healthy Volunteers
NCT07173543

IH, Brain Health, and T2D

Led by Darren P Casey · Updated on 2026-03-13

80

Participants Needed

1

Research Sites

144 weeks

Total Duration

On this page

Sponsors

D

Darren P Casey

Lead Sponsor

A

American Diabetes Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

IH, Brain Health, and T2D

Who Can Participate

Age: 60Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 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 60 and 85 years of age
  • Documented Type 2 diabetes (for diabetic group)
  • Scoring 26 or higher on the MoCA test
Not Eligible

You will not qualify if you...

  • Diagnosis of type 2 diabetes less than 1 year prior to enrollment (for diabetic group)
  • HbA1c less than 6.5% or greater than 10.0% (for diabetic group)
  • Body mass index greater than 40 kg/m2
  • Incident cardiovascular events in the last year such as heart attack or stroke
  • Symptomatic coronary artery disease and/or heart failure
  • Uncontrolled hypertension
  • Obstructive sleep apnea
  • Pulmonary disease
  • Dementia
  • Renal impairment with creatinine clearance (eGFR) less than 60 ml/min
  • Smoking or history of smoking within past one year
  • Diagnosis of diabetes (Type 1 or Type 2) for nondiabetic group

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Iowa

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

D

Darren Casey, PHD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

3

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