NCT03285009

Brief Summary

This project is a consequence of the research chair project studying the same phenomenon in adult volleyball players. The project will make use of and be part of the routine medical screening that is taken by the young players of the first degree of the Leuven Volleyball School, Belgium. All young players must undergo a routine medical investigation and movement screening. This is obliged by the law. The current project will use these data. Outcome parameters will be used to advice the trainer staff of the school to adjust their training interventions. This is normal routine too as the involved medical department has been advising the school for many years. Players will be followed up for 6 weeks. After those 6 weeks, the movement screening will be repeated to evaluate the change in the different outcome parameters. This last screening is not part of a normal routine as players normally are investigated more in a subjective way. The medical team and school want to change that routine. Data will be used to further improve training modalities and sports performance and reduce injury risk in these young athletes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
14

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2017

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 10, 2017

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 15, 2017

Completed
10 days until next milestone

Study Start

First participant enrolled

September 25, 2017

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 23, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 23, 2018

Completed
Last Updated

November 3, 2020

Status Verified

November 1, 2020

Enrollment Period

1.2 years

First QC Date

September 10, 2017

Last Update Submit

November 2, 2020

Conditions

Outcome Measures

Primary Outcomes (6)

  • Change of joint mobility

    Mobility will be assessed by using goniometer measurements (degrees of movement)

    Difference between baseline and 6 weeks

  • Change of strength

    Strength will be assessed by using handheld dynamo-meter data (Newton)

    Difference between baseline and 6 weeks

  • Change in balance score

    Stability is measured using the score on the Star Excursion Balance Test (numeric score on balance scale)

    Difference between baseline and 6 weeks

  • Change in lower limb joint angles during a single leg drop vertical jump

    Movement quality is measured using joint angles (trunk, pelvis, hip, knee, ankle)

    Difference between baseline and 6 weeks

  • Change in lumbopelvic stability score

    Lumbopelvic stability is scored using 9 clinical tests (Bend knee fall out, Active straight leg raise, prone knee bend, sitting knee extension, standing bow, pelvic tilt, one leg stance, backward rocking, forward rocking). Each test is given a score between 0 (poor performance) and 2 (good performance) adding up to a total score of 18.

    Difference between baseline and 6 weeks

  • Change in lower limb joint angles during a drop jump

    Movement quality is measured using joint angles (trunk, pelvis, hip, knee, ankle)

    Difference between baseline and 6 weeks

Secondary Outcomes (2)

  • Individualized web diagram of all outcome measurements

    Baseline

  • Number of injuries

    Baseline information from medical investigation

Study Arms (1)

Training intervention

OTHER

See information elsewhere

Other: Training intervention

Interventions

Based on the baseline screening, which is part of the normal prevention routine within the school, all athletes are given individual advice with regard to points of attention within training. For example: those athletes with reduced balance, will get more balance training. Intervention is individual as said and will be guided and supervised by the physical trainer and medical staff of the school.

Training intervention

Eligibility Criteria

Age11 Years - 13 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • All students from the first degree of the Volleyball school will participate
  • Male and female athletes will be included
  • Signing of an informed consent and assent form (for young kids) to use data for research
  • Agreement given by the medical staff to use data and allowing the kids to be accepted by the school

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

UZ Leuven

Leuven, 3000, Belgium

Location

MeSH Terms

Conditions

Wounds and Injuries

Study Officials

  • Filip F Staes, prof

    KU Leuven

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Masking not possible as individual treatment is given
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, Head of Musculoskeletal Research Group

Study Record Dates

First Submitted

September 10, 2017

First Posted

September 15, 2017

Study Start

September 25, 2017

Primary Completion

December 23, 2018

Study Completion

December 23, 2018

Last Updated

November 3, 2020

Record last verified: 2020-11

Data Sharing

IPD Sharing
Will not share

No individual data will be shared with other researchers. Data will be available to the medical and trainers staff. For research purposes, all data will be made anonymous.

Locations