AthletesKYAthNCT04162080
Kayak Polo Athletes
An observational study of Athletes, run by University of Valencia at 2 sites in Spain.
Trial summary
Kayak polo (KP) is a sport that, as a breviary, can be defined as the union between water polo and canoeing. The objective of this study is to compare anthropometric parameters, joint assessment, strength and functional capacity between two groups of KP players from the Valencian Community. Read more about this study
- Who is it for?
- Ages 16 to 30 years
- Conditions the study is for
- Athletes
- How many people
- 40 participants
- Where
- 2 sitesSpain
- Study dates
- 1 Dec 2019to 30 Dec 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 16 to 30 years
- All sexes
- Child, Adult
Study population: Observational cross-sectional study
Who may be able to join
- kayak polo athletes
Who cannot join
- other sports
- current injuries the previous 6 months
Trial locations and contacts
2 sites in 1 country.
About this study
Official title: Observational Study in Kayak Polo Athletes.
Kayak polo (KP) is a sport that, as a breviary, can be defined as the union between water polo and canoeing. The objective of this study is to compare anthropometric parameters, joint assessment, strength and functional capacity between two groups of KP players from the Valencian Community. The sample will be divided into a Sub21 group and a Senior group. Anthropometric variables (body mass index [BMI], percentage of fat mass, waist - hip index [CHF], body perimeters ...), shoulder assessment (Range of movement in rotations, Scapular Dyskinesis Test [SDT]) will be assessed. glenohumeral instability ...), hip assessment (modified Thomas test), strength (Hand Grip Strength test and upper limb thrust), lower limb power (Counter Movement Jump [CMJ]) and functional capacity (1 'push-ups for limbs upper and 1 'Sit-to-Stand test for lower limbs).
- Conditions
- Athletes
- Keywords
- kayak polo
What is being measured
The primary outcome is the main question the study is designed to answer.
Weight and percentage of fat mass
A scale - bioimpedaniometer model Tanita BF350 Anazyliser body composition will be used. Through acoustic bioimpedance, the four sensors of this scale that come into contact with the soles of the feet serve to assess the body composition of the individual, once the data on: size, age and sex have been entered.
Measured: 1 day
Skin fold
An 842-SK-001 polymer pyrometer of the Quirumed brand will be used. This one has an accuracy of 2mm and will be used for the measurement of skin folds of adipose tissue. Specifically, the tricipital fatty fold (PGT) will be measured
Measured: 1 day
Shoulder ROM
To obtain the ROM in shoulder rotations, a conventional analog polymer goniometer of the Saehan brand Grip model will be used, with an accuracy of 2 degrees. External rotation (RE) and internal rotation (RI) of the dominant upper limb will be assessed.
Measured: 1 day
Secondary outcomes (9)
Scapular dyskinesia
To assess the scapular dyskinesia, one of the most expanded tests in terms of the evaluation of the scapular kinematics will be used: the SDT. It consists of an observational assessment: the subject to study will be placed in standing position with his back to the examiner and performed between 5-10 shoulder abductions and the same number of shoulder flexions bilaterally (Figure 2-1) with a light load on each hand; The examiner is positioned so that he can observe the scapular kinematics without interference. Once done, it is classified as: absence of scapular dyskinesia or presence of scapular dyskinesia (subtle or obvious). It is a test with moderate inter-examiner reliability and high intra-examiner reliability.
Measured: 1 day
Glenohumeral apprehension test
The glenohumeral apprehension test (IGH) is used to evaluate IGH. This test consisted of placing the subject in standing position with 90º shoulder abduction and 90º elbow flexion passively. From this position, the examiner performs a posteroanterior displacement of the head of the humerus. The test is positive if the examinee shows signs of apprehension (running away from the posture, rotating to avoid displacement of the humeral head, ...) or indicating subjective sensation of instability
Measured: 1 day
Impingement subacromial (SAPS)
Based on the work of Diercks R et al and concluding that a single test is not sufficient to identify the presence of shoulder pathology, the combination of different tests is chosen to make a more reliable diagnosis for SAPS.
Measured: 1 day
Shortening in hip flexion
To assess the possible shortening of the hip flexor muscles, the modified Thomas test with pelvic stabilization will be used, since without external stabilization authors have determined that it is easy to obtain false positives.
The subject under examination is placed supine on the stretcher with approximately 3/4 of the lower limbs outside the stretcher. From that position a cinch is placed that stabilizes at the level of the anterior superior iliac spines, it is instructed to bring the knees to the chest and hold one of them with the hands. The leg to be evaluated is the one that is extended and the presence of passive hip flexion or not is assessed.
Two measurements are made per lower limb, the test was positive if the subject unintentionally is unable to keep the thigh of the leg to be tested in contact with the stretcher.
Measured: 1 day
Clamping force in upper limbs
It is used for the test of maximum grip strength in upper limb (HGS). With the subject in sitting position, with elbow flexion of 90, he is instructed to perform the maximum clamping force on the hydraulic hand dynamometer, so as to alter as little as possible the initial posture.
The dynamometer is of the analog hydraulic type of the Jamar model SP-5030J1, adjusting the grip according to the size of the subject's hand. This gives us a value that ranged from 0 to 90kg.
Measured: 1 day
Thrust force in upper limbs
To assess the thrust force of the upper limbs, an estimate of the maximum load (in kilograms) capable of moving a single vertical position in a flat bench press is performed, that is, the 1RM assessment is performed during the press exercise. hde banking. 1RM, Refers to the maximum load (in kg) that is able to move a subject in a given movement, which defines the maximum force of a subject for a particular exercise.
Measured: 1 day
Movement Jump (CMJ) or Countermovement Jump
It is done by starting with the subject from an upright position with the hands on the iliac crests. From this position the subject performs a flexion quickly followed by an extension of lower limbs which triggers the jump. At no time does the subject help himself with the upper limbs to apply inertia. This assessment is done by using the iPhone application "My Jump 2". First, a profile is created in the application for each subject where it is introduced: body weight, lower limb length measured with tape measure from the trochanter to fingertips with maximum plantar flexion and height from the ground to the trochanter with lower limbs in half-squat with both knees at 90 degrees of flexion. The smartphone and the subject are placed following the scheme shown in Figure 2-3. The subject performs the CMJ and the smartphone by using the slow motion the exact height (in centimeters) of the jump made in a valid way is calculated
Measured: 1 day
Functional capacity in lower limbs
The functional capacity of lower limbs is established by the 1 minute Sit-to-stand test. This assessment consists of getting up and sitting from a chair (45 cm high) as many times as possible for a minute. Two series are performed and the average of both measurements is obtained.
This objectification, validated by several authors, offers us a value that is directly proportional to the functional capacity. That is, greater number of repetitions means greater functional capacity of lower limbs.
Measured: 1 day
Functional ability in upper limbs
The functional capacity of upper limbs is established by the 1 minute Push-up test. Push-ups are performed with 4 supports on the floor: both feet and both hands. From this plate position flexion - extension of upper limbs is performed as many times as possible for one minute.
This objectification, validated by several authors, offers us a value that is directly proportional to the functional capacity. That is, greater number of repetitions means greater functional capacity of lower limbs.
Measured: 1 day
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Nov 2019
- Study start1 Dec 2019
- Primary completion20 Dec 2019
- Study completion30 Dec 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AthletesStudies of the same condition, open and under way.
- More trials run by University of ValenciaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 40 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Valencia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, GEMMA V ESPÍ LÓPEZ, PhD, University of Valencia
- Investigators
- Gemma V Espí-López, Dr, Principal investigator, Faculty of Physiotherapy. University of Valencia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04162080
- Sponsor's protocol ID
- ID0028
- Acronym
- KYAth
- Status last verified
- Feb 2020
- First submitted
- 10 Nov 2019
- Last updated
- 19 Feb 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 19 Feb 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Observational Study in Kayak Polo Athletes.
- ClinicalTrials.gov ID
- NCT04162080
- Acronym / sponsor ID
- KYAth / ID0028
- Conditions
- Athletes
- Keywords
- kayak polo
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 40 participants (actual)
- Lead sponsor
- University of ValenciaUniversity, hospital or other
- Study start
- 1 Dec 2019 (actual)
- Primary completion
- 20 Dec 2019 (actual)
- Study completion
- 30 Dec 2019 (actual)
- First posted
- 14 Nov 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Kayak polo (KP) is a sport that, as a breviary, can be defined as the union between water polo and canoeing. The objective of this study is to compare anthropometric parameters, joint assessment, strength and functional capacity between two groups of KP players from the Valencian Community. The sample will be divided into a Sub21 group and a Senior group. Anthropometric variables (body mass index [BMI], percentage of fat mass, waist - hip index [CHF], body perimeters ...), shoulder assessment (Range of movement in rotations, Scapular Dyskinesis Test [SDT]) will be assessed. glenohumeral instability ...), hip assessment (modified Thomas test), strength (Hand Grip Strength test and upper limb thrust), lower limb power (Counter Movement Jump [CMJ]) and functional capacity (1 'push-ups for limbs upper and 1 'Sit-to-Stand test for lower limbs).
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
Who may qualify
- Ages
- 16 to 30 years
- Sex
- All
- Age groups
- Child, Adult
- Study population
- Observational cross-sectional study
Key inclusion criteria (1 listed)
- kayak polo athletes
Key exclusion criteria (2 listed)
- other sports
- current injuries the previous 6 months
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Weight and percentage of fat mass
Time frame: 1 day
A scale - bioimpedaniometer model Tanita BF350 Anazyliser body composition will be used. Through acoustic bioimpedance, the four sensors of this scale that come into contact with the soles of the feet serve to assess the body composition of the individual, once the data on: size, age and sex have been entered.
Skin fold
Time frame: 1 day
An 842-SK-001 polymer pyrometer of the Quirumed brand will be used. This one has an accuracy of 2mm and will be used for the measurement of skin folds of adipose tissue. Specifically, the tricipital fatty fold (PGT) will be measured
Shoulder ROM
Time frame: 1 day
To obtain the ROM in shoulder rotations, a conventional analog polymer goniometer of the Saehan brand Grip model will be used, with an accuracy of 2 degrees. External rotation (RE) and internal rotation (RI) of the dominant upper limb will be assessed.
9 secondary outcomes
Scapular dyskinesia
Time frame: 1 day
Glenohumeral apprehension test
Time frame: 1 day
Impingement subacromial (SAPS)
Time frame: 1 day
Shortening in hip flexion
Time frame: 1 day
Clamping force in upper limbs
Time frame: 1 day
Thrust force in upper limbs
Time frame: 1 day
Movement Jump (CMJ) or Countermovement Jump
Time frame: 1 day
Functional capacity in lower limbs
Time frame: 1 day
Functional ability in upper limbs
Time frame: 1 day
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Feb 2020.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gemma V Espí-López, Dr principal investigator
Faculty of Physiotherapy. University of Valencia
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Athletes, run by University of Valencia at 2 sites in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 19 Feb 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Weight and percentage of fat mass (time frame: 1 day). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Feb 2020.