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- Essai clinique NCT05377645
The Effects of Cervical Mobilization on Cognitive Performance
The Effects of Cervical Mobilization on Cognitive Performance and Anxiety in Individuals With Non-Specific Neck Pain
Non spesific cervical pain syndromes are the most common cervical pathologies encountered in clinical practice. Non spesific cervical pain syndrome occurs as a result of postural deformities.
Massage and mobilization techniques are used in the treatment of Non spesific cervical pain syndrome due to their analgesic effects. The Cyriax mobilization technique is a manual therapy method applies to correct the limitation of movement in the joint and to relieve pain and functional disorders. Many studies have shown that Cyriax mobilization technique provides faster and momentary painless joint movement compared to other physical therapy modalities. Cervical mobilisation techniques also have regulator effect on autonomic nerve system. Cervical mobilisation also has positive effects on anxiety and tension.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
In this study, 32 patients with age range 18-65 who applied to Kırşehir Ahi Evran University Training and Research Hospital were examined. The individuals included in the study were divided into two groups according to the paired randomization method. These groups were control and intervention groups. Traditional physiotherapy methods were applied to the control group, traditional physiotherapy and Cyriax mobilisation techniques were applied to the intervention group. Traditional physiotherapy methods were included; Transcutaneous Electrical Nerve Stimulation (TENS), Ultrasound (US), isometric strengthening exercises.
For the evaluation of patients; Visual Analogue Scale (VAS), cervical goniometric measurements, Lowett muscle test, Burdon Test and Beck Anxiety Test were used.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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İç Anadolu
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Kırşehir, İç Anadolu, Turquie, 40500
- Kırşehir Ahi Evran Üniversitesi
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Who had cervical pain longer than six weeks
- Getting at least five points from Neck Disability Index
Exclusion Criteria:
- Who had neck surgery,
- Who had traumatic spinal cord injury,
- Clinical diagnosis of radiculopathy,
- Clinical diagnosis of myelopathy (sensory or motor deficit),
- Clinical diagnosis of neurological or rheumatologic disease and structural scoliosis
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Expérimental: Cervical mobilization
Mobilization Cyriax's cervical mobilization technique and traditional physiotherapy were applied to the intervention group.
For Cyriax Mobilization technique, the patient was asked to lying supine position.
Cervical ROM applied all directions.
Also AP and ML glides applied to the cervical region.
The treatment was done 3 times a week for 2 weeks.
Also traditional physiotherapy techniques were applied to the experimental group.
Traditional physiotherapy techniques were applied to the intervention group.
Conventional TENS type was used.
Continuous ultrasound type was applied with full contact technique.. And; isometric cervical strengthening exercises applied.
The treatment was done 3 times a week for 2 weeks.
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TENS, US, exercise
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Comparateur actif: Traditional physiotherapy
Traditional physiotherapy techniques were applied to the intervention group.
Conventional TENS type was used.
Current transition time was set as 50-100 µs.
TENS application is performed at a frequency of 100 Hertz for 20 minutes in amplitude that does not cause muscle contraction in the patient and creates a feeling of numbness and tingling.
Continuous ultrasound type was applied with full contact technique.
Ultrasound treatment was applied over the suboccipital area with circular movements towards the proximal and distal at a speed of 1-2.5 cm per second, at a dose of 1 W / cm2, for 6 minutes, with a frequency of 3 MHz.
And; isometric cervical strengthening exercises applied.
The treatment was done 3 times a week for 2 weeks.
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TENS, US, exercise
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Visual Analogue Scale (VAS)
Délai: 0-2 weeks
|
A Visual Analogue Scale (VAS) is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured.
It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms.
When responding to a VAS item, respondents specify their level of agreement to a statement by indicating a position along a continuous line between two end-points.
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0-2 weeks
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Collaborateurs et enquêteurs
Parrainer
Publications et liens utiles
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
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 12068451747
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
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