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A Psychophysiological Database of Maximal Effort Tests.

Constructing a Psychophysiological Database Towards the Optimization of the Methodological Approach During, and Training Advice After Maximal Effort Tests.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04226534
Enrollment
100
Registered
2020-01-13
Start date
2020-01-01
Completion date
2040-01-01
Last updated
2020-05-28

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

Conditions

Sports Physical Therapy

Brief summary

The aim of this study is first to construct a database containing psychophysiological data from athletes performing a maximal effort test. Second, the investigators want to use the data to optimize the methodological approach during, and trainings advice after maximal effort tests.

Detailed description

The lab (and research group) of Human Physiology and Sports Physiotherapy of the Vrije Universiteit Brussel performs exercise tests in both trained and untrained populations. The aim of the maximal effort test is to evaluate endurance capacity and provide recommendations to monitor training load. Until now, this is done by objective parameters such as heart rate, speed, time, power, etcetera. Researchers already presented a method to quantify training intensity distribution in elite endurance athletes based on the rating of perceived exertion. However, during pilot testing and everyday experience, these cut-off values are not always applicable to each individual athlete, nor are they the same for different sports. Therefore, the investigators want to investigate the possible relation between the exercise intensity, and objective and subjective parameters. Thereafter, the investigators want to provide recommendations to a new way of methodological approach during, and trainings advice after maximal effort tests.

Interventions

Performing a maximal effort test on the treadmill

Sponsors

Vrije Universiteit Brussel
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy * Trained * No medication influencing heart rate or physical performance

Exclusion criteria

* Disease * injury * medication influencing (maximal) heart rate or exercise performance Decision made after sports medical evaluation, comprising personal and family history, physical examination and resting electrocardiogram (ECG).

Design outcomes

Primary

MeasureTime frameDescription
ErgospirometryUp to one houroxygen consumption and carbon di-oxide production (ml/min/kg)

Secondary

MeasureTime frameDescription
blood samplesUp to one hourLactate concentration (mmol)
Rating of perceived effortUp to one hourRating of Perceived exertion on a scale from six to twenty

Countries

Belgium

Contacts

Primary ContactLuk Buyse, Msc. dr.
luk.buyse@vub.be+32 2 629 22 22
Backup ContactJo Ghillebert, Msc.
jo.ghillebert@vub.be+32 2 629 22 22

Outcome results

None listed

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