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Neck Muscle Activation in Patients With Long Standing Problems After a Whiplash Trauma Registered With Ultrasound With Speckle Tracking

10 mars 2017 mis à jour par: Anneli Peolsson, Linkoeping University
Today there is evidence for that neck specific exercises reduce neck pain problems in patients with mechanical neck pain. However, there is a lack of consensus on how to optimize neck exercises and dosages in neck rehabilitation. More knowledge is needed to determine which and how muscles are activated in exercises thought to be neck-specific. There is neither enough knowledge of differences in neck muscle activation between patients with long standing neck problems after a whiplash trauma and healthy controls nor if the neck muscle function improved with specific neck exercises. One approach would be a real time study of deformation and deformation rate in different layers of neck muscles in patients with residual long-term neck pain and disability after a whiplash trauma. The purpose of the present study was to investigate deformation and deformation rate in different layers of dorsal and ventral neck muscles (including upper and middle part of trapezius muscle) during rest and during different exercises; arm flexion until 120 degrees, repeated arm flexion until 90 degrees, low loaded neck extension, low loaded neck muscle endurance test, shoulder elevation. Forty patients with long standing (more than 6 months but less than 3 years)patients and 40 controls matched for age and gender will be included for comparisons between patients and healthy in neck muscle activation. The investigators also include 60 patients with whiplash trauma, of those 30 patients will be randomized to A. neck specific exercises in a 3 months period and B. will 30 be on a waiting list for 3 months. Measurements are performed at baseline and at 3 months follow-up. Those patients who fulfilled the 3 months period of neck specific exercises will also be asked for a 6 months follow-up.

Aperçu de l'étude

Statut

Complété

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Anticipé)

60

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

    • Östergötland
      • Linköping, Östergötland, Suède, SE-58183
        • Anneli Peolsson

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 à 63 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • WAD II and III
  • Age 18-63 years
  • Remaining problems
  • Right handed
  • Pain on right or on both sides.

Exclusion Criteria:

  • Myelopathy
  • Earlier fracture or luxation of the cervical column, earlier neck injury
  • Spinal tumour
  • Spinal infection
  • Surgery in the cervical column
  • Malignity
  • Systemic disease or other disease or another injury contraindicated to perform the treatment program or the measurements
  • Diagnosed severe psychiatric disorder
  • Unconscious in connection to the trauma
  • Known drug abuse
  • Lack of familiarity with the Swedish language

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: Diagnostique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Neck Specific exercises
3 months of neck specific exercises for 30 patients.
Neck specific exercises 2 times/week for 3 month at a physiotherapist. Home exercises.
Autres noms:
  • Physiotherapy with neck specific exercises
Aucune intervention: Waiting list
Thirty patients on the waiting list for 3 month before they have their intervention
Aucune intervention: Healthy controls
Forty healthy controls. Comparisons between forty included WAD patients and 40 healthy controls matched for age and gender will be investigated at baseline.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Speckle tracking analysis of muscle function
Délai: Baseline and at 3 and 6 months follow-up. The outcome measure is going to report a change over time.
Measured with medical ultrasonography
Baseline and at 3 and 6 months follow-up. The outcome measure is going to report a change over time.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Background data
Délai: Baseline
Background data of age, gender, social situation, work, work situation, sick-leave, income, pain history, debute of symptoms, about the accident, earlier treatment, other diseases or pain problems, expectations of treatment
Baseline
Symptom satisfaction
Délai: Baseline and at 3 months follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 months follow-up. The outcome measure is going to report a change over time.
Pain intensity on visual analogue scale (VAS)
Délai: Baseline and at 3 months follow-up. The outcome measure is going to report a change over time.
Symptoms in general, Neck, Arm, Headache
Baseline and at 3 months follow-up. The outcome measure is going to report a change over time.
Dizziness/ unsteadiness on visual analogue scale
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Pain distribution on drawing
Délai: Baseline and at 3 months follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 months follow-up. The outcome measure is going to report a change over time.
Pain Disability Index
Délai: Baseline and at 3 months follow-up. The outcome measure is going to report a change over time
Baseline and at 3 months follow-up. The outcome measure is going to report a change over time
Neck Disability Index
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Tampa Scale of Kinesiophobia (TSK-11 short version)
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Pain Catastrophizing Scale
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Hospital Anxiety and Depression Scale
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Euroquol
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Euroquol 5D and thermometer
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Exercise Self-Efficacy Scale
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
"How confident you are to exercise when things get in the way" Exercise self-efficacy scale is a six item scale with a five point scale (1=not at all confident and 5=completely confident).
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Self-Efficacy Scale
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
"People´s beliefs about their capabilities to produce designated levels of performance that exercise influence over events that affect their lives" Self-efficacy scale (by Altmaier) is a 20 item, 11 point scale (0=not at all confident, 10=completely confident).
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Work Ability Index
Délai: Baseline and at 3 month follow-up. The outcome is going to report a change over time.
Baseline and at 3 month follow-up. The outcome is going to report a change over time.
Physical Activity level
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Physical Outcome Measures
Délai: Baseline and at 3 month follow-up. The outcome is going to report a change over time.
Active range of motion of the neck, Head repositioning accuracy, hand strength, neck muscle endurance, sharpened Romberg, walking in a figure of eight, neurological examination: reflexes, sensibility and motor function
Baseline and at 3 month follow-up. The outcome is going to report a change over time.
SF-36
Délai: Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.
Baseline and at 3 month follow-up. The outcome measure is going to report a change over time.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chaise d'étude: Anneli Peolsson, Assoc. Prof., Linkoeping University

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

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

1 février 2011

Achèvement primaire (Réel)

1 décembre 2015

Achèvement de l'étude (Réel)

1 décembre 2015

Dates d'inscription aux études

Première soumission

28 février 2012

Première soumission répondant aux critères de contrôle qualité

4 mars 2012

Première publication (Estimation)

8 mars 2012

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

13 mars 2017

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 mars 2017

Dernière vérification

1 mars 2017

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • Ultrasound on neck muscles WAD

Plan pour les données individuelles des participants (IPD)

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INDÉCIS

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