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Recruiting NCT06808399

NCT06808399 The Magnitude of Inter-limb Asymmetry and Its Assocation with Inter-limb Asymmetry in Distance Runners and Non-runners

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Clinical Trial Summary
NCT ID NCT06808399
Status Recruiting
Phase
Sponsor Vrije Universiteit Brussel
Condition Healthy
Study Type OBSERVATIONAL
Enrollment 72 participants
Start Date 2023-01-01
Primary Completion 2025-06-01

Eligibility & Interventions

Sex All sexes
Min Age 20 Years
Max Age 50 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 72 participants in total. It began in 2023-01-01 with a primary completion date of 2025-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Distance running is one of the most popular and most accessible ways to engage in physical activity. Although distance running offers numerous health-related benefits and protects against noncommunicable diseases (e.g., type 2 diabetic, obesity, hypertension), research has indicated a high prevalence of running-related injuries with a more pronounced incidence among novice runners (i.e., 17.8 injuries per 1000h) compared to their highly trained peers (i.e., 7.2 injuries per 1000h). Interlimb asymmetry has previously been related to higher injury risk as well as to impaired sports performances. Nevertheless, to date, research on the degree and evolution of functional asymmetry (e.g., unequal strength between limbs) in distance runners is scarce and the role of functional asymmetries in running performance and running-related injuries remains unclear. Moreover, and despite the great number of unilateral tests available in the literature, there currently exists no reliable and run-specific field-based test battery to examine the degree of lower limb asymmetry in distance runners. Therefore, this study aims to assess the test-retest, intra- and inter-rater reliability of a newly created running-specific field-based test battery to assess the presence and degree of functional lower limb asymmetry among novice, moderatly and highly trained distance runners as well as a control group of non-athletes. The second objective is to assess the association between inter-limb asymmetry and running performance.

Eligibility Criteria

Inclusion Criteria: * • Being aged between 20 and 50 years at Tfamiliarization * Being free from any medical attention injury (i.e., injury that results in a participant receiving medical attention) for at least 6 months upon Tfamiliarization * Speaking Dutch, French or English * Highly trained distance runners: * Running at least 150km per month for at least 3 months Moderately-trained runners: * Running between 40 - 150 km per month for at least 6 months \- Novice distance runners: * Running not more than 10km per week for the past 12 months \- Control group of non-athletes * Performing \<75min of systematic moderate to vigorous-intensity physical activity per week and having no experience in systematic (un)structured running activities for the past 5 years Exclusion Criteria: * • Being younger than 20 years or older than 50 years at Tfamiliarization * Any known relevant medical history or current condition (e.g., neurological diseases, inner ear diseases) that could affect the performance of the functional tests (e.g., balance in repeated hop tests) * Participants that have undergone a surgery at lower limb level during the past 6 months * Medication or drug use (e.g., blood pressure medicines)that could affect the performance of the functional tests (e.g., balance in repeated hop tests) * Participants performing more than two hours per week of unilateral sports (e.g., tennis or soccer)

Contact & Investigator

Central Contact

Joachim D'Hondt

✉ Joachim.dhondt@vub.be

📞 +32 (0) 629 27 35

Frequently Asked Questions

Who can join the NCT06808399 clinical trial?

This trial is open to participants of all sexes, aged 20 Years or older, up to 50 Years, studying Healthy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06808399 currently recruiting?

Yes, NCT06808399 is actively recruiting participants. Contact the research team at Joachim.dhondt@vub.be for enrollment information.

Where is the NCT06808399 trial being conducted?

This trial is being conducted at Ixelles-Elsene, Belgium.

Who is sponsoring the NCT06808399 clinical trial?

NCT06808399 is sponsored by Vrije Universiteit Brussel. The trial plans to enroll 72 participants.

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