- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05788419
Sonographic Study of Hip Joint in Hockey Players
A Sonographic Study of the Hip Joints in Ice Hockey League Players
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The examined hip joint structure will be examined monographically and simultaneously using functional tests, the Patrick test, a passive test of the range of motion in the hip joint to external and internal rotation in the joint, FADDIR test. Approximately 20 probands will be enrolled in the study based on voluntary participation from a group of players of the Charles University hockey team Prague, who have a valid medical examination with no restrictions on eligibility for selected sporting activities. The second group will consist of approximately 20 additional probands from the U20 age group of ice hockey players enrolled voluntarily with a valid medical examination with no restrictions on eligibility for the selected sporting activities. In addition, approximately 20 volunteers of the same age range will be included in the study and form the control group. In total, there will be approximately 60 participants in the study.
The conditions for inclusion in the first and second test groups will be an age range of 19-28 years, playing ice hockey for 6 years at least three times a week in the standard training regime of Czech ice hockey clubs. The player must be a registered player, i.e. his/her health condition must be suitable for ice hockey. The exclusion criteria for the test group will be persons outside the defined age limit with acute or chronic illnesses for any reason and persons with post-traumatic hip and pelvic conditions.
The inclusion criteria for the third control group will be the same age range of 19-28 years and no acute, especially infectious, diseases and persons with post-traumatic hip and pelvic conditions. This will be a normal recreational sporting population with no registration affiliation in any sport.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Czech Republic
-
Prague, Czech Republic, Czechia, 16000
- Charles University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- a valid medical examination with no restrictions on eligibility for selected sports activities
- playing ice hockey from the age of 6 at least three times a week in the standard training regime of Czech ice hockey clubs
- registered player, i.e. his/her health must be fit to play ice hockey.
Exclusion Criteria:
- persons outside the defined age limit
- with acute or chronic illnesses for any reason
- persons with post-traumatic hip and pelvic conditions
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
examination group
Group of active hockey players
|
imaging method, functional test of hip joint
Other Names:
|
control group
Group of athletes, non hockey players
|
imaging method, functional test of hip joint
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
sonography picture identification
Time Frame: 20 min
|
identification of a higher prevalence of structural changes of the hip joint in hockey players
|
20 min
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
comparison of the functional tests
Time Frame: 20 min
|
Determining whether functional tests correlate with sonographic findings
|
20 min
|
Collaborators and Investigators
Investigators
- Principal Investigator: Jitka Malá, Dr, Charles University Prague, Czech Republic
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hybner, sonography
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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