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NCT06246760 Clinical Trial

Assessment of Training Status

Body Composition Clinical Trial

Official title:
Prestación de Servicios científicos, evaluación y Control Del Rendimiento

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06246760
Other study ID # PSC191100471
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2000
Est. completion date January 1, 2030

Study information
Verified date January 2024
Source Universidad Politecnica de Madrid
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this cross-over study is to evaluate the physiological response to exercise and body composition according to training status in participants with a wide spectrum of fitness states. The main questions it aims to answer are: - Which are the physiological differences across participants with different training status? - Which are the body composition differences across participants with different training status?

Description:

To satisfy the objective of the project, participants will perform an incremental test until volitional exhaustion. During this test, respiratory gases will be measured via a gas analyser as well as the cardiac response via an electrocardiogram. The same participants will have their body composition measured by dual X-ray densitometry (DXA).

Recruitment information / eligibility
Status Recruiting
Enrollment 1272
Est. completion date January 1, 2030
Est. primary completion date January 1, 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Be in enough physical fitness to perform the incremental test to volitional exhaustion. Exclusion Criteria: - Present any health condition preventing to perform the incremental exercise test until volitional exhaustion.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Exercise
Incremental exercise test until volitional exhaustion

Locations
Country Name City State
Spain Faculty of physical activity and sport sciences Madrid Comunity Of Madrid

Sponsors (1)
Lead Sponsor Collaborator
Universidad Politecnica de Madrid

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Training status Oxygen uptake at ventilatory threshold 1, ventilatory threshold 2 and maximal oxygen uptake breath-by-breath during the whole test
Primary Fat percentage fat percentage of an individual one determination before the test
Primary Fat free mass fat percentage of an individual one determination before the test
Primary Bone mineral density Bone mineral density of an individual one determination before the test
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