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

Non-specific Low Back Pain Clinical Trial

— MARLO  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03097263
• Other study ID #: CASILLAS Marlo 2016
• Status: Completed
• Phase: N/A
• First received: November 3, 2016
• Last updated: March 27, 2017
• Start date: January 2014
• Est. completion date: November 2016

Study information

• Verified date: March 2017
• Source: Centre Hospitalier Universitaire Dijon
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 127
• Est. completion date: November 2016
• Est. primary completion date: October 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

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

Related Conditions & MeSH terms

• Back Pain
• Functional Capacities
• Low Back Pain
• Non-specific Low Back Pain

Intervention

Other:
• Physical Rehabilitation program

Locations

Country	Name	City	State
France	Rehabiltiation department CHU Dijon	Dijon

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	COMFORTABLE WALKING SPEED (TEST OF 400M)		4 weeks
Secondary	200m fast walk test walking velocity		4 weeks
Secondary	Quebec score		4 weeks
Secondary	Shirado test		4 weeks
Secondary	Sorensen test		4 weeks