- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT04162080
Kayak Polo Athletes (KYAth)
Observational Study in Kayak Polo Athletes.
Aperçu de l'étude
Statut
Les conditions
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
-
-
-
Valencia, Espagne, 46010
- Gemma v. Espí López
-
Valencia, Espagne, 46010
- Gemma Espí
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- kayak polo athletes
Exclusion Criteria:
- other sports
- current injuries the previous 6 months
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Weight and percentage of fat mass
Délai: 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.
|
1 day
|
|
Skin fold
Délai: 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
|
1 day
|
|
Shoulder ROM
Délai: 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.
|
1 day
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Scapular dyskinesia
Délai: 1 day
|
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.
|
1 day
|
|
Glenohumeral apprehension test
Délai: 1 day
|
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
|
1 day
|
|
Impingement subacromial (SAPS)
Délai: 1 day
|
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.
|
1 day
|
|
Shortening in hip flexion
Délai: 1 day
|
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. |
1 day
|
|
Clamping force in upper limbs
Délai: 1 day
|
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. |
1 day
|
|
Thrust force in upper limbs
Délai: 1 day
|
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.
|
1 day
|
|
Movement Jump (CMJ) or Countermovement Jump
Délai: 1 day
|
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
|
1 day
|
|
Functional capacity in lower limbs
Délai: 1 day
|
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. |
1 day
|
|
Functional ability in upper limbs
Délai: 1 day
|
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. |
1 day
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- ID0028
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .