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Study of Effectiveness of Pold in Chronic Nonspecific Low Back Pain

NCT01591824 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2019-04-09

No results posted yet for this study

Summary

Through this research is to conduct a pilot clinical trial in the treatment of chronic nonspecific low back pain (degenerative and mechanical), by comparing two groups, one that will apply a technique of physiotherapy by passive movement of the column with oscillations in axial rotation at a frequency of 1.5 to 2 cps (resonance) of low amplitude (called "Pold Concept"), another group that applies the standard protocol of treatment for this condition, as used in the hospital where performed the study.

It will compare the levels of efficiency and effectiveness of each treatment and the comparison between them. This will measure the perception of pain intensity and disability.

Conditions

  • Mechanical Low Back Pain

Interventions

OTHER

Resonant oscillation

Resonant sustained oscillations are applied in the following areas * general column. * lumbar muscles, and paraspinal muscles, * sacral decompression oscillatory * Opening by lateral vertebral lumbar rhythmic swing. * Balancing and pelvic decompression * Swing-lumbar vertebral rotation.

OTHER

column exercise group

* paraspinal muscle stretching exercises * postural correction * mobilization exercises thoracic and lumbar * Motor control exercises

Sponsors & Collaborators

  • Omphis Foundation

    lead OTHER

Principal Investigators

  • José M. Muniesa, physiatrist · Esperanza Hospital (Barcelona)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-05-31
Primary Completion
2015-07-31
Completion
2015-09-30

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01591824 on ClinicalTrials.gov