Load During Sweep Rowing and the Influence on the Posture

January 5, 2023 updated by: Charles University, Czech Republic

Influence of Regularly Repeated Asymmetric Load on the Locomotor System in Sweep Rowers

The aim is to assess the influence of asymmetric training on the locomotor system in sweep rowers. To analyse possible changes objectively, the axial position of the hull will be assessed using Moiré topography, and the symmetry of foot loading will be monitored with a pedobarograph. Furthermore, the Visual Analog scale and Cluster of Laslett will determine whether an asymmetric load can provoke pain in the lumbar region or cause a blockage in the SI joint. In the experimental study, there will be three different groups of participants. Selected sweep rowers will make the first study group. The second group will consist of scull rowers, and the last control group will consist of people with no experience with rowing. The selected participants will undergo the first measurement at the turn of the spring and summer seasons when intensive preparation for rowing competitions begins, in which sweep rowers train mainly on water and asymmetrically. The measurement results in the three groups will be further compared with each other to evaluate whether statistically significant differences can be found.

Study Overview

Detailed Description

Methods: 21 sweep rowers, 20 scull rowers and 23 non-rowing peers were enrolled on the study of this diploma thesis. Each subject was assessed using DIERS formetic 4D and DIERS pedoscan devices. Additionally, participants in each group were assessed by FAIR test, Cluster of Laslett, trigger point palpation of the m. piriformis and Visual analogue scale were used to assess pain intensity in the lumbar region.

Study Type

Observational

Enrollment (Actual)

64

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

      • Praha, Czechia
        • Charles University, Faculty of physical education and sport

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 25 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Rowers training in the junior and senior category of competitive rowing together with probands from the general population and students of UK FTVS who have never rowed.

Description

Inclusion Criteria for rowers:

  • Training and racing exclusively in the unpaired disciplines of competitive rowing in the Czech Republic for a group of unpaired rowers
  • Training and racing exclusively in the pairs disciplines of competitive rowing in the Czech Republic for the group of pairs rowers
  • Dedication to rowing for more than three years
  • Frequency of training at least three times a week or more

Inclusion Criteria for non-rowers:

-Engaging in sports recreationally without higher intensity training (less than three times a week) or at all.

Exclusion Criteria for rowers:

  • The presence of lumbar spine pain at a time when the athlete was not yet exercising
  • Presence of musculoskeletal pain caused by a condition for which the athlete is actively being treated (Morbus Bechterev, spondylodiscitis, etc.)
  • Presence of a previously diagnosed internal, orthopaedic or neurological disease
  • Lateral spinal misalignment caused by a previously diagnosed disease (congenital scoliosis, idiopathic scoliosis, Morbus Scheuermann, etc.)

Exclusion Criteria for non-rowers:

  • Active participation in sports associated with an asymmetric load, such as tennis, floorball, hockey and others (training once a week or more)
  • Presence of pain caused by a disease for which the person is actively treated (Morbus Bechterev, spondylodiscitis, etc.)
  • Presence of a previously diagnosed internal, orthopaedic or neurological disease
  • Lateral spinal misalignment caused by a previously diagnosed disease (congenital scoliosis, idiopathic scoliosis, Morbus Scheuermann, etc.)

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: Other

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
sweep rowers
Each subject was assessed using DIERS formetic 4D and DIERS pedoscan devices. Additionally, participants in each group were assessed by FAIR test, Cluster of Laslett, trigger point palpation of the m. piriformis and Visual analogue scale.
Assessment of mentioned tests and their comparison.
Other Names:
  • trigger point palpation of the m. piriformis
  • DIERS pedoscan device
  • Visual analogue scale
  • FAIR test
  • Cluster of Laslett test
scull rowers
Each subject was assessed using DIERS formetic 4D and DIERS pedoscan devices. Additionally, participants in each group were assessed by FAIR test, Cluster of Laslett, trigger point palpation of the m. piriformis and Visual analogue scale.
Assessment of mentioned tests and their comparison.
Other Names:
  • trigger point palpation of the m. piriformis
  • DIERS pedoscan device
  • Visual analogue scale
  • FAIR test
  • Cluster of Laslett test
control non-rowers
Each subject was assessed using DIERS formetic 4D and DIERS pedoscan devices. Additionally, participants in each group were assessed by FAIR test, Cluster of Laslett, trigger point palpation of the m. piriformis and Visual analogue scale.
Assessment of mentioned tests and their comparison.
Other Names:
  • trigger point palpation of the m. piriformis
  • DIERS pedoscan device
  • Visual analogue scale
  • FAIR test
  • Cluster of Laslett test

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Rotation deviation of the trunk at the level of L3 vertebrae and sway area of COP
Time Frame: one-time measurement
observation of changed position of the trunk and pelvis
one-time measurement
Scoliotic angle in sweep rowers during walking
Time Frame: one-time measurement
observation of rotational deviation of the trunk during walking
one-time measurement
Trunk deviation in the frontal plane and COP deviation
Time Frame: one-time measurement
observation of later-lateral deviation of he trunk
one-time measurement
Magnitude of scoliotic angle
Time Frame: one-time measurement
observation of the level of scoliotic deviation
one-time measurement
Cluster of Laslett testing
Time Frame: one-time measurement
observation of the mobility of sacroiliac joint
one-time measurement

Collaborators and Investigators

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

Investigators

  • Study Director: Jitka Malá, PhDr., Charles University Prague, Czech Republic

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 1, 2021

Primary Completion (Actual)

February 28, 2022

Study Completion (Actual)

March 31, 2022

Study Registration Dates

First Submitted

December 31, 2022

First Submitted That Met QC Criteria

January 5, 2023

First Posted (Estimate)

January 16, 2023

Study Record Updates

Last Update Posted (Estimate)

January 16, 2023

Last Update Submitted That Met QC Criteria

January 5, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

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 Postural; Defect

Clinical Trials on DIERS formetic 4D

Subscribe