Effectiveness of a 6-week Specific Rehabilitation Program Combining Education and Exercises on Walking Capacity in Patients with Lumbar Spinal Stenosis with Neurogenic Claudication

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The aim of this study is to determine the effectiveness of a 6-week specific rehabilitation program combining education and exercises on walking capacity in patients with LSS causing NC. The intervention group will receive standardized education and specific exercises while the control group will only receive standardized education. The program in both groups will last for 6 weeks with 4 evaluation timepoints (baseline, week 2, week 4 and post-intervention assessment). The primary outcomes will be walking capacity measured with the Self-Paced Walking Test and the secondary outcomes will be back and leg pain intensity, LSS-related disability, self-efficacy, level of physical activity, anxiety and depression, physical activity level, gait pattern characteristics, balance, and global perceived change.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

• being at least 50 years old

• having a degenerative central LSS alone or in combination with other LSS types (e.g. foraminal, lateral) and/or a spondylolisthesis affecting one or multiple vertebral levels, confirmed by clinical history, physical examination and proper imaging

• having NC associated with LSS

• being able to speak and understand French

• being willing to attend 3 intervention sessions per week

• with a duration of signs and symptoms of at least 3 months

• (7) being able to walk at least 20 meters without walking aid, but not being able to walk continuously for 30 minutes

• being able to provide informed written consent.

Locations
Other Locations
Canada
Université du Québec à Trois-Rivières
RECRUITING
Trois-rivières
Contact Information
Primary
Mariève Houle, PhD(c)
marieve.houle@uqtr.ca
819 376-5011
Time Frame
Start Date: 2023-01-26
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 66
Treatments
Experimental: Intervention Group
Intervention group will received education and a specific rehabilitation program (exercises).
Other: Control Group
Control group will received education alone.
Related Therapeutic Areas
Sponsors
Leads: Université du Québec à Trois-Rivières

This content was sourced from clinicaltrials.gov