Home
Clinical Trials
NCT06159374

Effects of Physical Training in Altered Environmental Conditions on Exercise Performance

NCT ID: NCT06159374

Last Updated: 2023-12-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

128 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-01-01

Study Completion Date

2025-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The main objective of the study is to evaluate the physiological-biochemical effects of physical training under artificially altered climatic conditions (using a hypoxic thermoclimatic chamber) in particular to determine the effect of such training on exercise capacity and physiological response, including the effect of training in high-performance athletes. The study will evaluate the effects of physical training and the simultaneous application of hypoxia and heat/cold on aerobic and anaerobic capacity and the physiological response of the human body. The aim of the study is to find the most favourable environmental conditions for physical training in order to maximise physical performance.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Hypoxia, Altitude Cold Exposure Heat Exposure

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

training exercise human performance aerobic capacity anaerobic capacity maximal oxygen uptake muscle power

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control

Control group

Group Type NO_INTERVENTION

No interventions assigned to this group

normoxia-thermoneutral

Training performed under normoxia (200 m above sea level) and thermoneutral conditions (21°C) and constant humidity (40%);

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

hypoxia-thermoneutral

Training performed under normobaric hypoxia (3000 m above sea level) and thermoneutral conditions (21°C) and constant humidity (40%);

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

normoxia-heat

training performed under normoxia (200 m above sea level) and high ambient temperature (31°C) and constant humidity (40%);

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

hypoxia-heat

training performed under normobaric hypoxia (3,000 m above sea level) and high ambient temperature (31°C) and constant humidity (40%);

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

normoxia-cold

Training performed in normoxia (200 m above sea level) and low ambient temperature (-11°C) and constant humidity (40%).

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

hypoxia-cold

training performed under normobaric hypoxia (3,000 m above sea level) and low ambient temperature (-11°C) and constant humidity (40%);

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

hypoxia-heat-humidity

training performed under normobaric hypoxia (3,000 m above sea level) and high ambient temperature (31°C) and high humidity (70%);

Group Type EXPERIMENTAL

exercise and environmental conditions

Intervention Type OTHER

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

exercise and environmental conditions

Participants will perform interval training for 4 weeks in a variety of environmental conditions. There will be a measurement of aerobic and anaerobic capacity before and after the training. Before and after the first and last workout, blood will be drawn for biochemical analysis.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

absence of medical contraindications to high-intensity physical exertion. The medical examination is required (included an exercise ECG, blood tests to exclude anemia or low hemoglobin and iron concentration)

Exclusion Criteria

any training (including hypoxia training or exposure) performed in the 6 months prior to the beginning of the intervention

Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University School of Physical Education, Krakow, Poland

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Marcin Maciejczyk, Prof. dr

Role: STUDY_DIRECTOR

Departament of Physiology and Biochemistry

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University School of Physical Education in Cracow

Krakow, , Poland

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Poland

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Anna Radoń, MSc

Role: CONTACT

Phone: +45126831142

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Anna Radon

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

MEIN 2021/DPI/229

Identifier Type: -

Identifier Source: org_study_id