Loads, Injuries and Illnesses Among Elite Handball Players (PPDC-2022)

March 28, 2024 updated by: Armin Paravlic, University of Ljubljana

Effects of Physical, Psychosocial and Dual-career Loads on Injuries and Illnesses Among Elite Handball Players

Primary goal of the research is to determine whether injury/illness occurrence is influenced by the academic, training and competition loads, as well as the overall load (sum of academic/work, training and competition loads) in elite handball athletes To examine whether subjective measures of perceived overall stress correlate with objectively measured levels of stress.

Determine the benefits of certain biomarkers to monitor stress, load and injury/illness occurrence in athletes.

Study Overview

Detailed Description

The current structure and organizational initiatives do not meet the needs of athletes as they face different challenges throughout their careers. There is a need for better health surveillance, load monitoring and support services with a focus on injury/illnesses prevention and rehabilitation. The main goal of the research is to determine how specific loads affect the occurrence of injuries and illnesses in elite handball players and how much of the total load an athlete can withstand before an injury/illness occurs. Thus, the study will attempt to identify athletes at risk of injury/illness by monitoring their workload with subjective (perceived stress) and objective (biomarkers, hours of workload) measurements. One of the goals is also to determine the correlation between objective measures of stress (biomarkers) and subjective measures of stress (athlete's stress assessment). The results will not only be important for the medical and sports community for development of new injury prevention and rehabilitation strategies, but also for structuring the correct policy recommendations for athletes' general health. The research will be carried out on approx. 250 elite handball players (the entire 1st men's handball league) during one handball season. In addition to other parameters (monitoring of load, injuries and illnesses), blood samples will be taken from athletes at five time points according to their training cycle.

Study Type

Observational

Enrollment (Actual)

189

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Ljubljana, Slovenia, 1000
        • Faculty of Sport
      • Ljubljana, Slovenia, 1000
        • Handball Clubs

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The first league handball players

Description

Inclusion Criteria:

  • At least national-level handball players above 18 years of age, who are in a dual-career setting.
  • Handball players older than 18 years old, who are competing at least at national level and are not in a dual-career setting will be matched by their demographic characteristics and included in the control group.

Exclusion Criteria:

  • Not fulfilling inclusion critieria

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Handball players
Professional handball players
There is no any intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Oslo Sports Trauma Research Center Questionnaire on Health Problems (OSTRC)
Time Frame: 12 months
Injury and illness questionnaire
12 months
Load
Time Frame: 12 months
PHYSICAL, PSYCHOSOCIAL AND DUAL-CAREER loads
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Biomarkers
Time Frame: 12 months
testosterone, cortisol, Immunoglobulin A (IgA)
12 months
Life Events Survey for Collegiate Athletes (LESCA) questionnaire
Time Frame: 12 months
Life Events Survey for Collegiate Athletes questionnaire
12 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Body composition
Time Frame: 12 months
Body composition measurements with bio-impedance
12 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Kristina Drole, MSc, Faculty of Sport, University of Ljubljana

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 20, 2022

Primary Completion (Actual)

June 4, 2023

Study Completion (Actual)

September 1, 2023

Study Registration Dates

First Submitted

July 17, 2022

First Submitted That Met QC Criteria

July 20, 2022

First Posted (Actual)

July 22, 2022

Study Record Updates

Last Update Posted (Actual)

April 1, 2024

Last Update Submitted That Met QC Criteria

March 28, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

Data will be available upon the reasonable request to principal investigator

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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