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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02393521
Other study ID # H1421077978677
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2014
Est. completion date December 2019

Study information

Verified date May 2022
Source University of Valencia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Completed
Enrollment 13
Est. completion date December 2019
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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


Intervention

Device:
Shindo® vibration mattress
vibration therapy was self-administered while the subject was laying in supine in a polyurethane mattress

Locations

Country Name City State
Spain Universitat de Valencia Valencia

Sponsors (1)

Lead Sponsor Collaborator
University of Valencia

Country where clinical trial is conducted

Spain, 

References & Publications (1)

Imtiyaz S, Veqar Z, Shareef MY. To Compare the Effect of Vibration Therapy and Massage in Prevention of Delayed Onset Muscle Soreness (DOMS). J Clin Diagn Res. 2014 Jan;8(1):133-6. doi: 10.7860/JCDR/2014/7294.3971. Epub 2014 Jan 12. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Pressure Pain Threshold (PPT) Pain tolerance was measured at baseline (T0) and after the first (T1), five (T5) and 10 treatment sessions (T10). 10 days
Secondary Neck Disability Index (NDI) Perceived neck pain and disability were measured at baseline (T0) and after the first (T1), five (T5) and 10 treatment sessions (T10). 10 days
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