Clinical trial Recruiting at 1 site Interventional Ages 18 to 40

Trained vs Untrained: How Endurance Status Affects Lung Blood Flow During Blood Volume Changes

Official title: Central Blood Volume Shifts in Healthy Adults With Varying Levels of Fitness: Effects on Lung Diffusing Capacity

Run by University of Alberta · NCT07897357 · Data updated 2026-11-12

This study tests whether highly trained athletes show different lung blood flow responses when blood return to the heart changes, compared with untrained individuals.

Quick facts

Study typeInterventional
Ages18 Years to 40 Years
SexAll
Enrollment200 (estimated)
SponsorUniversity of Alberta
Academic / other
Locations1 site (Edmonton, Alberta)
StatusRecruiting
StartedOctober 9, 2026
Main results expectedDecember 15, 2027
Study endsJune 1, 2028
Registry record updatedNovember 5, 2026
Trial IDNCT07897357 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18-40 who are either endurance-trained or untrained, without major chronic diseases or recent blood donations, and able to complete pulmonary and exercise testing.

Probably not a fit

Individuals with severe obesity, recent smoking or cannabis use, pregnancy, significant cardiovascular or pulmonary disease, or other listed exclusions may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study explores how endurance training status and sex influence pulmonary diffusing capacity and its components during acute central blood volume changes induced by lower body pressure and body tilt. Participants undergo multiple visits, including screening, pulmonary function tests, and graded exercise testing, with interventions using lower body positive and negative pressure and positional changes. The goal is to see if trained athletes have greater DLCO changes than untrained individuals and whether females differ from males in these responses. The research will be conducted at the University of Alberta's Clinical Physiology Laboratory in Edmonton over up to four months, with careful screening and safety measures in place.

Why it matters

Potential benefit: If successful, findings could improve understanding of how fitness level influences lung-circulation responses during body position changes and blood volume shifts.

How similar studies have gone: Prior research has examined DLCO responses to physiological stress, but this study tests a specific combination of training status, sex, and controlled blood volume changes, which represents a novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 18-40 years old.

Exclusion Criteria:

* Severe obesity (body mass index \>35 kg/m2).
* Self-reported blood donation or transfusion in the past 60 days. Large artificial fluctuations in blood volume may impact the findings of the present study.
* Pregnancy. To confirm this, women not using contraception will be given a pregnancy test. Pregnancy presents additional complications and may confound the results of the study; therefore, pregnant women will be excluded.
* Known chronic disease (heart failure, hypertension, diabetes, asthma, chronic obstructive pulmonary disease, renal disease).
* Participants with known postural orthostatic tachycardic syndrome or orthostatic hypotension.
* Participants who currently smoke cigarettes (within the last month) or those who have \>1 pack-year smoking history.
* Participants who currently smoke cannabis products (within the last month) or those who have \>1 joint-year cannabis history.

Where it's running

  • Clinical Physiology Laboratory
    Edmonton, Alberta, Canada
    Recruiting

Study contacts

  • Principal investigator: Michael K Stickland, PhD — University of Alberta
  • Study coordinator: Desi P Fuhr, MSc
  • Email: fuhr@ualberta.ca
  • Phone: 780-492-1121

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.