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Clinical Trials/NCT03149614
NCT03149614
Completed
N/A

Clinical Effects in Cervical Spinal Mobilization Versus Resonant Oscillation Mobilization (POLD) in Neck Pain. A Randomized Clinical Trial.

Universidad Rey Juan Carlos1 site in 1 country50 target enrollmentMay 10, 2017

Overview

Phase
N/A
Intervention
Not specified
Conditions
Manual Therapy
Sponsor
Universidad Rey Juan Carlos
Enrollment
50
Locations
1
Primary Endpoint
Changes in pain intensity before and after the intervention
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The aim of this study is to compare the clinical effects of spinal mobilization versus vertebral resonant oscillation (POLD) in patients with bilateral mechanical neck pain on pain sensitivity and neck pain intensity.

Detailed Description

The clinical practice guidelines for manual therapy management the neck pain including the spine mobilization. The vertebral resonant oscillation using the POLD method is similar to spine mobilizations, but there are some differens; the oscillatory movement has a sinusoidal waveform, the frequency used between 1.2 and 2 Hz and the amplitude is similar to "neutral zone" to described by Panjabi 1992. The spinal mobilizations has a posterior-anterior vertebral movement for spinous process, described by Maitland 2000.

Registry
clinicaltrials.gov
Start Date
May 10, 2017
End Date
October 25, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jaime Salom Moreno

PT, PhD

Universidad Rey Juan Carlos

Eligibility Criteria

Inclusion Criteria

  • neck pain symptoms of mechanical nature
  • age from 18 to 60 years
  • bilateral symptoms
  • symptoms for at least 3 month of duration

Exclusion Criteria

  • whiplash injury
  • previous spine surgery
  • diagnosis of cervical radiculopathy or myelopathy
  • having undergone any physical therapy intervention in the previous 6 month
  • pregnancy

Outcomes

Primary Outcomes

Changes in pain intensity before and after the intervention

Time Frame: Baseline, one week after the last session, 1 months and 3 months after the last session.

A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of neck pain

Secondary Outcomes

  • Changes in disability before and after the intervention(Baseline, one week after the last session, 1 months and 3 months after the last session.)

Study Sites (1)

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