MedPath

Dry Needling of Scalene Muscle Trigger Points in Mechanical Neck Pain

Not Applicable
Completed
Conditions
Neck Pain
Interventions
Other: Dry needling
Other: Manual Therapy
Registration Number
NCT03762252
Lead Sponsor
Universidad Rey Juan Carlos
Brief Summary

There is preliminary evidence suggesting that referred pain from active trigger points can play a relevant role in individuals with mechanical neck pain. Some studies have investigated the effectiveness of dry needling over the upper trapezius muscle in this population. However, other muscles, such as the scalene muscles, can be also relevant for neck pain symptoms. No study has investigated the effects of the application of dry needling over active trigger points in the scalenes muscles in a sample of patients with mechanical neck pain.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria

Generalized neck-shoulder pain with symptoms provoked by neck postures, neck movement, or palpation of the cervical musculature

Exclusion Criteria
  • whiplash injury;
  • previous cervical or thoracic surgery;
  • cervical radiculopathy or myelopathy;
  • diagnosis of fibromyalgia syndrome;
  • having undergone physical therapy in the previous 6 months;
  • less than 18 or greater than 45 years of age
  • fear to needles
  • any respiratory disease, e.g., chronic brochitis

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Dry needlingDry needlingPatients will receive dry needling over active trigger points in the scalene muscles
Manual TherapyManual TherapyPatients will receive a manual compression for 30seconds over active trigger points in the scalene muscles
Primary Outcome Measures
NameTimeMethod
Changes in neck pain intensity with a numerical pain rate scale before and after the interventionBaseline, one day (immediately post), 7 days (one week) and 30 days (one month) after the intervention

A Numerical Pain Rate Scale (NPRS, 0-10) will be used to assess spontaneous neck pain intensity

Secondary Outcome Measures
NameTimeMethod
Changes in inspiratory vital capacity with an incentive spirometer before and after the interventionBaseline, one day (immediately post), 7 days (one week) and 30 days (one month) after the intervention

Changes in inspiratory vital capacity will be assessed with the incentive spirometer DHD Coach 2®

Changes in oxigen saturation with a pulse oximeter before and after the interventionBaseline, one day (immediately post), 7 days (one week) and 30 days (one month) after the intervention

Oxygen saturation will be monitored with a handheld pulse oximeter with Masimo SET® measure-through Motion and Low Perfusion™ pulse oximeter

Changes in neck-related disability with the Neck Disability Index before and after the interventionBaseline and 7 days (one week) and 30 days (one month) after the intervention

The Neck Disability Index (NDI, 0-50), a specific neck pain related disability questionaire, will be used for assessing neck pain related-disability

Trial Locations

Locations (1)

César Fernández-de-las-Peñas

🇪🇸

Alcorcón, Madrid, Spain

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