Effects of Nervous System Mobilization
4 avril 2018 mis à jour par: Anabela G Silva, Aveiro University
Effect of Nervous System Mobilization on Heat, Cold and Mechanical Pain Thresholds and Lower Limb Flexibility
This study aims to compare the effect of tension neural mobilization versus sliding neural mobilization of the peroneal nerve on the heat and cold threshold, on pressure pain threshold and on flexibility both in the dominant lower limb (subjected to mobilization) and the non-dominant lower limb (not subjected to mobilization) in healthy young participants.
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Description détaillée
Sixty young and healthy participants will be randomly allocated to receive tension neural mobilization (n=30) or sliding neural mobilization (n=30).
Data on heat threshold, cold threshold, pressure pain threshold and lower limb flexibility will be collected before the intervention, immediately after the intervention and at least 24h after the intervention.
Type d'étude
Interventionnel
Inscription (Réel)
52
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
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-
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Aveiro, Le Portugal, 3810-193
- School of Health Sciences
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Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
18 ans et plus (Adulte, Adulte plus âgé)
Accepte les volontaires sains
Oui
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- naïve to nervous system mobilization;
Exclusion Criteria:
- Any surgery or trauma in the previous 6 months; neurological, cardiorespiratory or rheumatic pathology; cancer.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Neural mobilization - tension
It is anticipated that 30 participants will be in this group.
They will receive tension type neural mobilization of the peroneal nerve in the dominant limb.
This will consist of positioning the lower limb with inversion and plantar flexion of the ankle, extension of the knee and maximum flexion of the hip without pain.
A physiotherapists will move the hip from this maximum position of flexion in direction to extension (for example if the participants reaches 80º of flexion the mobilization will be between 40º and 80º of flexion).
Each participant will receive four series of 10 mobilizations with 1 minute rest between series.
|
Neural mobilization in tension consists of using combinations of joint movement known to maximize the tension and lengthening of peripheral nervous structures. The intervention will be delivered in one session only. |
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Comparateur actif: Neural mobilization - sliding
It is anticipated that 30 participants will be in this group.
They will receive sliding neural mobilization of the peroneal nerve in the dominant limb.
Each participant will receive four series of 10 mobilizations with 1 minute rest between series of the following combination of movement: from ankle dorsiflexion, knee extension and hip extension to ankle plantarflexion, knee and hip flexion.
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Gliding neural mobilization consists of using combinations of joint movement known to maximize the movement of the peripheral nerves in relation to adjacent structures. The intervention will be delivered in one session only. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Range of motion of the Straight Leg Raising test
Délai: Baseline
|
The hip is raised to maximum flexion and the degree of flexion is measured with universal goniometer
|
Baseline
|
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Range of motion of the Straight Leg Raising test
Délai: Approximately 45 minutes after baseline measurements
|
The hip is raised to maximum flexion and the degree of flexion is measured with universal goniometer
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Approximately 45 minutes after baseline measurements
|
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Range of motion of the Straight Leg Raising test
Délai: At least 24 hours after baseline measurements
|
The hip is raised to maximum flexion and the degree of flexion is measured with universal goniometer
|
At least 24 hours after baseline measurements
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Heat threshold
Délai: Baseline
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Baseline
|
|
Heat threshold
Délai: Approximately 45 minutes after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Approximately 45 minutes after baseline measurements
|
|
Heat threshold
Délai: At least 24 hours after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
At least 24 hours after baseline measurements
|
|
Cold threshold
Délai: Baseline
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Baseline
|
|
Cold threshold
Délai: Approximately 45 minutes after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
Approximately 45 minutes after baseline measurements
|
|
Cold threshold
Délai: At least 24 hours after baseline measurements
|
This is measured with a QSense instrument, which has thermode that is attached to the skin.
The temperature in this thermode increases or decreases (as per the protocol being used) and the participants is holding a device to stop the temperature to increase/decrease when he/she first perceives it.
The temperature perceived is the test result.
|
At least 24 hours after baseline measurements
|
|
Pressure pain threshold
Délai: Baseline
|
This is measured using a pressure pain algometer.
Pressure is made with this device against a specific body region (upper and lateral part of the dominant foot) until the participants perceives that the pressure changes to pain.
The amount of pressure that the participants perceives as being painful is the test result.
|
Baseline
|
|
Pressure pain threshold
Délai: Approximately 45 minutes after baseline measurements
|
This is measured using a pressure pain algometer.
Pressure is made with this device against a specific body region (upper and lateral part of the dominant foot) until the participants perceives that the pressure changes to pain.
The amount of pressure that the participants perceives as being painful is the test result.
|
Approximately 45 minutes after baseline measurements
|
|
Pressure pain threshold
Délai: At least 24 hours after baseline measurements
|
This is measured using a pressure pain algometer.
Pressure is made with this device against a specific body region (upper and lateral part of the dominant foot) until the participants perceives that the pressure changes to pain.
The amount of pressure that the participants perceives as being painful is the test result.
|
At least 24 hours after baseline measurements
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Anabela Silva, PhD, University of Aveiro
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Réel)
1 janvier 2017
Achèvement primaire (Réel)
1 juillet 2017
Achèvement de l'étude (Réel)
1 décembre 2017
Dates d'inscription aux études
Première soumission
19 janvier 2017
Première soumission répondant aux critères de contrôle qualité
20 janvier 2017
Première publication (Estimation)
24 janvier 2017
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
5 avril 2018
Dernière mise à jour soumise répondant aux critères de contrôle qualité
4 avril 2018
Dernière vérification
1 avril 2018
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- NSM01
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
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