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Evaluation of Spinal Mobility Reeducation in Patients Treated for a Lumbar Spinal Stenosis After Epidural Infiltration

NCT02610335 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2020-10-26

No results posted yet for this study

Summary

In actual practice the patients with mild or moderate lumbar spinal stenosis symptoms receive an epidural infiltration and participate in kyphosis reeducation in first intention. Yet the kyphosis reeducation did not show a real profit in the time compared with the natural evolution of the pathology. The study assume that the spinal mobility reeducation will reduce the incidence of pain recurrences compared with the classic kyphosis reeducation.

Conditions

  • Lumbar Spinal Stenosis

Interventions

OTHER

Control group (C)

* kyphosis reeducation on Huber platform during 2 weeks, * patient education : on physiopathology of the lumbar spinal stenosis and treatments as well as healthy lifestyle and prevention (plans of anatomy, plastic column, slides of medical imaging), * flexibility exercises, stretching exercises and abdominal muscles exercises : to continue at home (the exercises will be reported on a book that will be given to the patient), * exercises on cycle ergometer or walking on treadmill : to continue at home.

OTHER

Test group

* spinal mobility reeducation on Huber platform during 2 weeks, * patient education : on physiopathology of the lumbar spinal stenosis and treatments as well as healthy lifestyle and prevention (plans of anatomy, plastic column, slides of medical imaging), * flexibility exercises and mobilization exercises : to continue at home (the exercises will be reported on a book that will be given to the patient), * exercises on cycle ergometer or walking on treadmill : to continue at home.

Sponsors & Collaborators

  • University Hospital, Bordeaux

    lead OTHER

Principal Investigators

  • Mathieu DE-SÈZE, MD · service de médecine physique et de réadaptation, Centre Hospitalier Universitaire de Bordeaux,

  • Antoine BENARD, MD · USMR CHU Bordeaux

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-15
Primary Completion
2018-06-01
Completion
2018-06-01

Countries

  • France

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 NCT02610335 on ClinicalTrials.gov