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Is the Walking Velocity an Efficient Outcome of Rehabilitation Program in Non- Specific Low Back Pain Patient

Completed
Conditions
Non-specific Low Back Pain
Functional Capacities
Interventions
Other: Physical Rehabilitation program
Registration Number
NCT03097263
Lead Sponsor
Centre Hospitalier Universitaire Dijon
Brief Summary

Despite the prevalence of chronic low back pain, functional symptomatology of this disease remains poor and treatment decisions are based mainly on subjective data (importance and pain tolerance). However, there are some experimental elements that involve objective assessment of locomotor capabilities - at forefront objectives which the walking velocity in the evaluation of this pathology in terms of severity of functional impairment. Recent evidence suggest the effectiveness of physical rehabilitation program for improving patients functional capacities and their reintegration in socio-professional life. This retrospective study aims to quantify the evolution of the parameters collected during standardized walking tests performed before and after rehabilitation program. These patients have systematically carry out a comfortable walk test (400m walk test) and a brisk walk test (200m) at the beginning and end of their program. Furthermore, a maximal stress test on a treadmill was performed before the program in order to detect any cardiovascular events and to allow the personalization of the effort level required (target heart rate) during rehabilitation. In this study the evolution of the comfortable and fast speed will be collected and compared with the stress test data, and other measured parameters (functional score of Quebec, muscle Tests Shirado and Sorensen).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
127
Inclusion Criteria
  • Female or male
  • age between 18 and 70
  • Non-specific low back pain - achieved rehabilitation program
Exclusion Criteria
  • inflammatory diseases
  • cancer
  • infectious diseases

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
PatientsPhysical Rehabilitation programPatients included for rehabilitation program
Primary Outcome Measures
NameTimeMethod
COMFORTABLE WALKING SPEED (TEST OF 400M)4 weeks
Secondary Outcome Measures
NameTimeMethod
Quebec score4 weeks
Sorensen test4 weeks
200m fast walk test walking velocity4 weeks
Shirado test4 weeks

Trial Locations

Locations (1)

Rehabiltiation department CHU Dijon

🇫🇷

Dijon, France

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