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The Effect of Vibration Therapy Over Neck Myofascial Trigger Points

Not Applicable
Completed
Conditions
Neck Pain
Myofascial Trigger Point Pain
Interventions
Device: Shindo® vibration mattress
Registration Number
NCT02393521
Lead Sponsor
University of Valencia
Brief Summary

The aim of this study was to investigate the efficacy of a self-administered vibration therapy treatment on neck pain, disability and pressure pain thresholds in patients with non-specific neck pain and myofascial trigger points (MTrPs). The investigators hypothesized that patients receiving vibration therapy would report less perceived neck pain, disability and present higher PPTs after receiving vibration therapy when compared to a control no-treatment group.

Detailed Description

Myofascial trigger points (MTrPs) are a common source of (regional) pain in patients presenting with musculoskeletal pain. Mechanical vibration has been suggested as a treatment for pain relief. In this study, the effects of vibration therapy on people with non-specific neck pain and MTrPs were investigated. Seventeen chronic non-specific neck pain patients were randomly assigned to a treatment (vibration group, n = 9) or control group (n = 8). Vibration group received 10 self-administered sessions of vibration therapy (45-50 Hz for 15 minutes with the subject laying in supine). Perceived neck pain and disability and pressure pain thresholds over MTrPs of the upper trapezius and levator scapulae bilateraly were measured at baseline and after the first, five and 10 treatment sessions.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
13
Inclusion Criteria
  • a score of ≥ 5/50 in Neck Disability Index
  • active or latent myofascial trigger points in upper trapezius or levator scapulae muscles
Exclusion Criteria
  • previous cervical spine surgery
  • cervical radiculopathy
  • severe systemic disease
  • fibromyalgia
  • other widespread musculoskeletal pain syndromes
  • patients being treated with medication or physiotherapy within the last 4 weeks

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Vibration groupShindo® vibration mattressPatients in the vibration therapy group received 10 self-administered sessions of vibration therapy (45-50 Hz), one session per day, remaining on their Shindo® vibration mattress at home in supine for 15 min.
Primary Outcome Measures
NameTimeMethod
Pressure Pain Threshold (PPT)10 days

Pain tolerance was measured at baseline (T0) and after the first (T1), five (T5) and 10 treatment sessions (T10).

Secondary Outcome Measures
NameTimeMethod
Neck Disability Index (NDI)10 days

Perceived neck pain and disability were measured at baseline (T0) and after the first (T1), five (T5) and 10 treatment sessions (T10).

Trial Locations

Locations (1)

Universitat de Valencia

🇪🇸

Valencia, Spain

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