Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
Healthy Volunteers
NCT06317259

Effects of Hypoxic Breathwork

Led by University of California, San Diego · Updated on 2024-12-06

75

Participants Needed

1

Research Sites

76 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This project will study changes that occur during a short period of intensive daily slow-paced breathing and breath hold practice (i.e., "breathwork"). On the first and last days of the week-long practice, investigators will conduct high-density EEG recordings during breathwork to evaluate spectral power, coherence, and causality dynamics of the brain when it is naïve to breathwork and after adaptation to a breathwork practice. Breath, blood, urine, saliva, stool samples, biometric data, and sleep EEG will be collected before the start of daily breathwork practice and again after 1 week of breathwork practice to examine the effect of breathwork on full body biochemistry, molecular biology, and sleep. Investigators will also use questionnaires to assess the impact of breathwork on stress and sleep quality.

CONDITIONS

Official Title

Effects of Hypoxic Breathwork

Who Can Participate

Age: 18Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Persons aged 18 to 45 years
  • Available for the entire duration of the study
  • In good general health based on self-report
  • Willing and able to follow the breathwork routine
  • Agree to follow lifestyle considerations during the study
  • Provide signed and dated informed consent form
Not Eligible

You will not qualify if you...

  • Current or past regular breathwork practice
  • Current use of psychoactive medications such as anti-depressants or anxiolytics
  • Pregnancy
  • Habitual bedtime later than 11:30pm or regularly getting less than 6 hours of sleep per night
  • Feverish illness within the past 10 days
  • Regular smoker or tobacco user (more than 1 cigarette, gum, or pouch per month)
  • Blood pressure above 140 systolic and/or 90 diastolic
  • History of seizure disorder, asthma, or serious cardiac fibrillation disorders

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

UC San Diego

La Jolla, California, United States, 92093

Actively Recruiting

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Research Team

J

Julie Onton, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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