Skip to main content
Clinical Trials/NCT02564185
NCT02564185CompletedNot Applicable

Prospective, Randomized Study of the Impact of a Education Program for Patients Suffering From Low Back Pain

Hopital Foch1 site in 1 country98 target enrollmentStarted: September 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
98
Locations
1
Primary Endpoint
Quality of life

Study Overview

Brief Summary

According to the WHO, therapeutic education is intended to help patients acquire or maintain the skills they need to optimally manage living with a chronic disease. Low back pain is frequent and therapeutic education could be a promising option.

The purpose of the study is to evaluate the impact of a therapeutic education program for patients suffering from low back pain.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Low back pain
  • •Treatment with transcutaneous electrical nerve stimulation (TENS)

Exclusion Criteria

  • •Contra-indication of TENS
  • •Patients with mental disorders
  • •Lack of autonomy or patients living alone at home without help
  • •Concomitant inclusion in another research on the treatment of pain

Arms & Interventions

Control

Active Comparator

The "control" group will follow usual practice.

Intervention: Usual practice (Other)

Education program

Experimental

The "Education program" group benefit in addition of a therapeutic education program including nursing follow-up at 1, 3 and 6 months.

Intervention: Usual practice (Other)

Education program

Experimental

The "Education program" group benefit in addition of a therapeutic education program including nursing follow-up at 1, 3 and 6 months.

Intervention: Education program (Other)

Outcomes

Primary Outcomes

Quality of life

Time Frame: 6 months

EIFEL functional disability scale (Gagnon et al, Annals Phys Med Rehab, 2009, 1, 3-16).

Secondary Outcomes

  • Evaluation of the program(6 months)
  • Neuropathic pain(6 months)
  • Social impact(6 months)
  • Pain(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials

Prospective, Randomized Study of the... | Clinical Trial