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Clinical Trial

Effect of Acute Intermittent Hypoxia in Healthy Individuals

IRB Protocol Number STU00202448

Contact

Milap Sandhu msandhu@sralab.org

Objective

The primary study objectives seek evaluate the effect of Acute Intermittent Hypoxia on upper extremity strength and fatigability, in individuals without any significant neurologic injury or progressive neuromuscular disease.

Who Can Participate

The following eligibility criteria must be met in order to participate:

  • No history of neurologic injury or neuromuscular disorder
  • No history of significant cardiopulmonary disease (instability, congestive heart failure, sleep apnea)
  • Not a current smoker

Compensation

Reimbursement for participation is $10/hour for up to 7 hours, per visit, for up to 8 visits.

Age Range

Age Range 18-70 years

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