Injuries in Swedish Padel

April 20, 2022 updated by: Sofia Ryman Augustsson

Injury Prevalence and Risk Factors in Swedish Padel Recreational and Competition Players

The purpose of this project is to investigate the injury panorama of acute and overuse injuries in women and men who regularly participate padel. The intention is to provide insights on injury prevalence, injury location, injury consequences, gender differences and risk factors .

This study will be conducted as a retrospective cohort study where the participants consist of female and male padle players, both at the recreational and competition level, with at least 6 months' experience in the sport. The information from this project can be valuable in the work of identifying risk factors for padle injuries and injury prevention strategies.

Study Overview

Status

Completed

Conditions

Detailed Description

Study design and participants This study will be conducted as an observational study using a retrospective survey. The participants will consist of padle players at both recreational and competitive level. An estimated 300 players will participate (~ 50% women). Recruitment will take place through inquiries via padle associations, social media and information flyers posted on padle courts around the Stockholm and Kalmar region. The survey will be aimed at all regularly active women and men padle players, aged 18-65, with at least 6 months' experience in the sport. Players with <1 hour of padle training per week will be excluded.

Procedure During the autumn of 2021, data collection will start for the retrospective part and then continue for about 3 months. Injury registration will be carried out using a web-designed registration form (SurveyMonkey®). The survey is designed with a previously developed form for acute injuries and with the help of the online survey OSTRC Overuse Injury Questionnaire for injuries of an overuse nature. The participant will register any musculoskeletal injury and complaints that have occurred during the last 6 months. The players will also provide information about age, gender, number of training hours per week and experience of padle and other training routines.

Injury definition The injuries will be classified as either traumatic, i.e., the player could define a specific sudden onset of pain with a defined trauma included, or as due to overuse. The severity of the injury will be graded by the time of absence from training and match participation. The injuries will be divided into three categories. ''Minor'' is defined as an injury leading to an absence from training/matches of no more than 1 week. Injury leading to an absence of 2-4 weeks is defined as ''moderate''. ''Major'' is defined as an injury leading to an absence of more than 4 weeks.

Measurements The OSTRC survey was developed in Norway and has been translated and validated into Swedish. The sensitivity of this survey is assumed to be much greater than traditional questionnaires about injuries in sports and enables more overload injuries to be identified. In addition, the survey registers the extent of injury prevention strategies as well as training frequency, intensity, amount and type of training. The body regions that will be registered are neck, shoulder, elbow, hand/wrist, thoracic spine, lumbar spine, hip, thighs, knees and lower legs and foot/ankle. Participants will also estimate the severity of the problems on ordinal scale ranging from 0-4, where "0" is referring to no problem, for each body region. The acute injuries will be registered using previously developed forms for acute injuries.

Statistics Statistics will be calculated using SPSS®25.0 (IBM SPSS Statistics, New York, USA). Descriptive statistics (mean ± SD and range) will be calculated for each variable. To compare means between the groups (women and men, age groups, recreational versus competitive players), independent student T-tests will be used. Fisher's exact test will be used to compare different injury location between groups. Pearson's correlation coefficient will be used to assess associations between variables.To calculate if data is normally distributed, in the retrospective part, a Shapiro-Wilks test of normality will be performed. The level of significance will be set at p<0.05.

Study Type

Observational

Enrollment (Actual)

274

Contacts and Locations

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

Study Locations

      • Kalmar, Sweden, 391 82
        • Sofia Ryman Augustsson

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 to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The participants will consist of padle players at both recreational and competitive level. An estimated 300 players will be invited to participate (~ 50% women). Recruitment will take place through inquiries via padle associations, social media and information flyers posted on padle courts around the Stockholm and Kalmar region.

Description

Inclusion Criteria:

  • Regularly active women and men padle players
  • Aged 18-65
  • At least 6 months' experience in padel.

Exclusion Criteria:

  • Players with <1 hour of padle training per week.
  • Players with less then 6 months' experience of padle training.

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

  • Observational Models: Cohort
  • Time Perspectives: Retrospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Injuries occured during padel; training and/or match
Time Frame: Injuries during the last 6 month
Prevalence (number) of acute and overuse injuries
Injuries during the last 6 month
Body region injured
Time Frame: Last 6 month
Description of body region injured and prevalence; number of injuries at one site/of total number of injuries
Last 6 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Type of injury
Time Frame: Last 6 month
Number of different types of injury, prevalence; number of a specific type of injury/of total number of injuries
Last 6 month
Injury occurence in relation to different enviroment
Time Frame: Last 6 month
Prevalence (number) of acute and overuse injuries in relation to different enviroment
Last 6 month
Injury occurence in relation to different padel rackets
Time Frame: Last 6 month
Prevalence (number) of acute and overuse injuries in relation to different rackets
Last 6 month
Sex difference in injury occurence
Time Frame: Last 6 month
Prevalence (number) of acute and overuse injuries in men versus women
Last 6 month

Collaborators and Investigators

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

November 1, 2021

Primary Completion (Actual)

February 27, 2022

Study Completion (Actual)

February 28, 2022

Study Registration Dates

First Submitted

October 27, 2021

First Submitted That Met QC Criteria

October 27, 2021

First Posted (Actual)

November 8, 2021

Study Record Updates

Last Update Posted (Actual)

April 21, 2022

Last Update Submitted That Met QC Criteria

April 20, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2021-03382

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.

Clinical Trials on Injury;Sports

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