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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02554461
Other study ID # S56955
Secondary ID
Status Completed
Phase N/A
First received September 16, 2015
Last updated May 1, 2017
Start date August 2015
Est. completion date March 2017

Study information

Verified date October 2016
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

On the basis of clinical and movement analysis records players are informed on what parameters can be optimized in order to improve their performance and avoid injuries


Recruitment information / eligibility

Status Completed
Enrollment 37
Est. completion date March 2017
Est. primary completion date December 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Members of national volleyball team signing informed consent

Exclusion Criteria:

No specific exclusion criteria

Study Design


Related Conditions & MeSH terms

  • Optimisation of Performance and Avoidance of Injury

Intervention

Other:
advise for exercices given by team staff
To respond to questions asked: it is not the investigator who decides on the intervention, but the daily team staff (e.g. trainer, coach, PT,.....). So no predetermined intervention is provided

Locations

Country Name City State
Belgium KU Leuven/UZLeuven Leuven Vlaams-Brabant

Sponsors (1)

Lead Sponsor Collaborator
Prof. Dr. F. Staes

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary 2D and 3D joint angles of different movements together with kinetics kinematics and kinetics with regard to gait, running, jumping and arm movements. This means for example joint angles (measured by 3D motion analyses data, 2D measurement data) and kinetics (joint moments, pressure plate measurements) Time frames: these data will recorded by one measurement session. For information of clinicaltrials.gov (also other outcome measures): at this point it really is an observational study. It is a kind of "service project" for an elite athletes team. Advice is provided, but not as is meant within a real clinical trial. It might evolve to such a project, but at this state it is not the case. 1 day
Secondary muscle strength isokinetic measurements (expressed in Nm) 1 day
Secondary muscle strength isokinetic measurements (ratio agonist/antagonist as for example ratio between knee flexors/extensors) Time frames: these data will be recorded during one measurement session. This is during same session as for primary outcome measure. 1 day
Secondary joint stability nominal scale (good, poor) 1 day
Secondary joint control nominal scale (good, poor) 1 day
Secondary prevalence injury past interview (frequency/percentage of occurrence) 1 day
Secondary prevalence injury present interview (yes/no) 1 day
Secondary (segmental) length Meter 1 day
Secondary weight Kg 1 day
Secondary Body mass index Kg/m² 1 day