Skip to main content
Clinical Trials/NCT02518360
NCT02518360
Completed
Not Applicable

Effect of Osteopathic Treatment in Patients With Nonspecific Low Back Pain: Stabilometry

Universidad Miguel Hernandez de Elche0 sites50 target enrollmentSeptember 2015
ConditionsLower Back Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lower Back Pain
Sponsor
Universidad Miguel Hernandez de Elche
Enrollment
50
Primary Endpoint
Oswestry Questionnaire
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Determine the improvement in nonspecific low back pain patients with osteopathic techniques (Body Adjustment Protocol) and know changes in stabilometric measures analyzed with a stabilometric platform (Footscan®).

Detailed Description

Fifty patients participate in this study (25 experimental group with body adjustment protocol of osteopathy and 25 control group). For a first objective of this study, all the patients determine if the osteopathic approach to the body adjustment approach will improve low back pain (Oswestry Questionnaire). For the second aim, the investigators want to know if there are changes in the distribution of body weight in lower limbs in group experimental and control group, analyzed with a stabilometric platform (Footscan®). The experimental group is treated with osteopathy, three sessions (20 minutes/session) and a frequency one session/week. The treatment osteopathic is the body adjustment protocol. In the other hand, the control group made 2 stretching global postures once a week (10 minutes for each posture) for three weeks: the first was for the anterior muscular chain and the second posture to stretch the posterior muscle chain. Before treatment, immediately after the last session and a month later, are measured stabilometric parameters, height and Oswestry. The analysis will be made with Statistical Package for the Social Sciences (SPSS Statistics) 22.0

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
December 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Emilio-José Poveda-Pagán

PT - PhD

Universidad Miguel Hernandez de Elche

Eligibility Criteria

Inclusion Criteria

  • Aged between 18 and 65 years.
  • Patients with non-specific low back pain.
  • Patients with alteration in the distribution of loads in a podiatric platform.

Exclusion Criteria

  • Specific low back pain diagnosed.
  • Pregnancy.
  • Recent surgery in the last year.
  • Acute musculoskeletal disorders out of the lumbar region.
  • Patients with vestibular and instability problems.
  • Meniere syndrome.
  • Oncologic patients.
  • Patients with manual therapy treatment during the study.

Outcomes

Primary Outcomes

Oswestry Questionnaire

Time Frame: 5 minutes

Improvement of low back pain measured by Oswestry Questionnaire: The results of the lumbar scale Oswestry disability percentage will be obtained. Results of the initial measurement, final month of treatment and compared.

Secondary Outcomes

  • Centre of Pressure Displacement(5 minutes)

Similar Trials