Gait in Low Back Pain Patients After Spinal Mobilization
NCT02645123 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 75
Last updated 2017-06-08
Summary
Introduction: patients with chronic back pain as a result of degenerated disc disease, besides pain also present with impaired gait. The purpose of this study is to evaluate both the clinical data using clinical rating scales, such as Oswestry Disability Index Greek version (ODI), Numerical Pain Rating Scale for low back pain and leg pain (NPRS) and the Roland Morris Disability Questionnaire Greek Version, and kinetic and kinematic characteristics during gait analysis in patients with chronic low back pain as a result of the degenerated disc disease (Disc Degenerative Disease), before and after application of manual therapy techniques.
Methodology: for the purposes of the study, 75 patients suffering from chronic low back pain were randomly divided into 3 groups of 25 each. Each group received five sessions with the first group receiving manual therapy treatment (spinal mobilisation), the second a sham treatment and the third, classic physiotherapy (stretching exercises, TENS and massage). To evaluate the effectiveness of each treatment, the visual analog pain scale, two questionnaires (Oswestry and Roland Morris) and also an optoelectronic system for recording and analysis of gait (kinetic and kinematic data) were utilized.
Conditions
- Chronic Low Back Pain
Interventions
- DEVICE
-
TENS
Enraf-Nonius Sonopuls 692
- PROCEDURE
-
spinal mobilization
passive physiological intervertebral movements and passive accessory posteroanterior mobilization
- PROCEDURE
-
swedish type massage
petrissage, effleurage, tapotement
- PROCEDURE
-
static hamstring stretch
static hamstring stretching
- PROCEDURE
-
sham treatment
touching of the skin overlying the lumbar area
Sponsors & Collaborators
-
University of Ioannina
lead OTHER
Principal Investigators
-
GEORGIOS O KREKOUKIAS, PT, MSc, PhD · University of Ioannina
-
IOANNIS D GELALIS, MD, PhD · University of Ioannina
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 21 Years
- Max Age
- 78 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-12-31
- Primary Completion
- 2014-10-31
- Completion
- 2014-11-30
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