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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05685563
Other study ID # Mikulík, rowing
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 1, 2021
Est. completion date March 31, 2022

Study information

Verified date January 2023
Source Charles University, Czech Republic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 64
Est. completion date March 31, 2022
Est. primary completion date February 28, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility 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 Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
DIERS formetic 4D
Assessment of mentioned tests and their comparison.

Locations

Country Name City State
Czechia Charles University, Faculty of physical education and sport Praha

Sponsors (1)

Lead Sponsor Collaborator
Charles University, Czech Republic

Country where clinical trial is conducted

Czechia, 

Outcome

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