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The Impact of Physical Training Under Normobaric Hypoxia on Oxidative Stress Level, Inflammatory State, Intestinal Damage, and Mitochondrial Metabolism in Young Males

The Influence of Physical Training in Normobaric Hypoxia on Prooxidant-Antioxidant Imbalance, Inflammatory Marker Levels, Intestinal Damage Degree, and Mitochondrial Energy Release Rate in Young Non-trained Males

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06204731
Enrollment
50
Registered
2024-01-12
Start date
2023-02-01
Completion date
2026-12-31
Last updated
2024-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoxia, Altitude

Keywords

inflammation, oxidative stress, intestinal damage, muscle damage, mitochondrial metabolism, normobaric hypoxia, training

Brief summary

* Cognitive assessment of the influence of a 4-week proprietary training program under normobaric hypoxia conditions on the levels of inflammatory markers, disturbances in prooxidant-antioxidant balance, degree of intestinal damage, and mitochondrial energy production rate in young sedentary males. * Applied objective: Development of practical training guidelines utilizing training in normobaric hypoxia conditions to enhance mechanisms related to oxygen transport, adaptive changes within the immune system, body's antioxidant capacity, gut permeability, substrate utilization efficiency, and mitochondrial function for coaches and athletes.

Interventions

Participants will engage in interval training and will reside and sleep at different altitudes for a period of 4 weeks. Aerobic and anaerobic capacity tests and an eccentric exercise test will be performed before and after the training intervention. Before and after the training program, somatic measurements will also be taken. Before and after the first and last workout, blood will be drawn for biochemical analysis.

Sponsors

Ministry of Education and Science,Poland
CollaboratorUNKNOWN
University School of Physical Education, Krakow, Poland
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
19 Years to 29 Years
Healthy volunteers
Yes

Inclusion criteria

* no known metabolic diseases, no contraindications to physical exercise and no history of high altitude sickness stated in interview. A medical examination (including ECG, blood and urine tests) is required.

Exclusion criteria

* changes in diet during the experiment, smoking and abuse of alcohol and/or other stimulants.

Design outcomes

Primary

MeasureTime frameDescription
Measurement of aerobic capacity (endurance)7 days before training and 7-10 days after the training. Training will last 4 weeks.Measurement of maximal oxygen uptake and determination of ventilatory thresholds (ergospirometry)
Measurement of anaerobic capacity7 days before training and 7-10 days after the training. Training will last 4 weeksMeasurement of maximal anaerobic power (Wingate Anaerobic Test)
Blood analysis7 days before training and 7- 10 days after the training. The training will last 4 weeks and will consist of 12 workouts.Indicators of prooxidant-antioxidant imbalance, markers of inflammatory status, markers of muscle damage, markers of intestinal damage, HIF (hypoxia-inducible factor), EPO (erythropoietin), markers of mitochondrial metabolism, morphology (including reticulocytes).
Somatic indices7 days before training and 7-10 days after the training. Training will last 4 weeks.Body composition analysis ( body height \[m\], body mass \[kg\], Quetelet II Index \[kg/m\^2\], lean body mass \[kg\], fat mass \[kg\], fat percentage \[%\] and total water content \[kg\]

Countries

Poland

Contacts

Primary ContactAnna Radoń, MSc
anna.radon@awf.krakow.pl+45126831142
Backup ContactAnna Kałuża, MSc
anna.kaluza@doctoral.awf.krakow.pl

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026