- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05685563
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
Status
Completed
Conditions
Intervention / Treatment
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:
|
|
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:
|
|
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:
|
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- Mikulík, rowing
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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