Effects of Dry Needling on Stiffness in Latent Trigger Points
- Conditions
- Trigger Points
- Interventions
- Device: Intervention-Dry NeedlingDevice: Control-Dry Needling
- Registration Number
- NCT04394741
- Lead Sponsor
- University of Castilla-La Mancha
- Brief Summary
The purpose of this study is to determine whether application of Dry Needling (DN) is effective for reduced on Stiffness in Latent trigger point (LTrP) of upper trapezius. The secondary purposes are to determine the correlation on two elastography for stiffness measure (Shear-wave elastography and Strain elastography). Randomized controlled trial, in parallel with cross-control design. Two groups with LTrP in upper trapezius, and will be randomly selected to DN group or Sham-Dn group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 51
- Age between 18 and 30 years
- The presence of LTrP in the middle third of the upper trapezius muscle on the dominant side
- Being able to provide written informed consent
- Being able to follow instructions and realize clinical tests
- Any pharmacological therapeutic
- Any medical treatment or physical therapies at cervical region during the 6-month before this study - Any diagnosed health problem
- Any history of head and upper extremity surgery or trauma
- Any red flags to DN, (ie: metabolic diseases, pregnancy, kinesiophobia, Infection, cancer)
- Absence of recurrent history of neck pain
- No neck pain symptomatology the previous 6 months
- Cervical disk herniation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Deep Dry Needling Intervention-Dry Needling Intervention-Dry Needling: Deep Dry Needing into the latent trigger point of the upper trapezius muscle Sham Dry Needling Intervention-Dry Needling Control-Dry Needling: Sham Dry Needling into the latent trigger point of the upper trapezius muscle Sham Dry Needling Control-Dry Needling Control-Dry Needling: Sham Dry Needling into the latent trigger point of the upper trapezius muscle
- Primary Outcome Measures
Name Time Method Change on Stiffness (Shear wave elastography and Strain Elastography) Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment Shear-wave Elastography (SWE) as assessed using an Logiq S8 US system (GE Healthcare).
The stiffness was determined with measuring velocity of shear waves in trapezius muscle on SWE exam.
Strain elastography (SEL) as assessed using an Logiq S8 US system (GE Healthcare).
The stiffness was determined by applying light repetitive compression with the hand-held transducer
- Secondary Outcome Measures
Name Time Method Change in Thickness of muscle Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment The muscle was scanned in the longitudinal and axial planes, taking care to avoid anisotropy. B-Mode gray scale was employed to measure muscle thickness
Change in Post-needling soreness Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment The procedure performed was the subject had to characterize the level of pain using a visual analog scale (VAS), ranging from 0mm (no pain) to 10mm (worst imaginable pain)
Change in Pain Pressure Threshold (PPT) Baseline, at 30 minutes after treatment, at 24 hours after treatment, at 72 hours after treatment Pressure-Pain Threshold as assessed by an manual mechanical algometer. PPT is the minimal amount of pressure that produces pain and is used to assess abnormalities in nociceptive processing or hyperalgesia.
Trial Locations
- Locations (1)
Performance and Sport Rehabilitation Laboratory
🇪🇸Toledo, Spain