Simple rehab program shows promise for spinal stenosis sufferers
NCT ID NCT05513326
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a 6-week program that combines specific exercises with education to see if it improves walking ability in people with lumbar spinal stenosis and nerve-related leg pain. Fifty-one adults aged 50 and older took part. The intervention group received both exercises and education, while the control group received only education. Researchers measured walking capacity, pain, disability, and other factors at several points during the program.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- exercise and education program
- What this could lead to
- If successful, this program could offer a non-surgical way to improve walking and reduce pain for people with lumbar spinal stenosis.
- What could go wrong
- This is a small, early-stage study with only 51 participants. Results may not apply to everyone, and the program requires a 6-week commitment with multiple sessions per week.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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51 people
The number who actually took part.
- Started
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Jan 2023
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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. Exclusion Criteria: * congenital LSS, * symptomatic osteoarthritis (hip or knee) causing limited walking capacity * neurological disease affecting walking capacity such as Parkinson * uncontrolled diabetes * heart failure * intermittent claudication of vascular origin * impaired cognitive capacity * back or lower extremities surgery in the past 3 months
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Université du Québec à Trois-Rivières
Trois-Rivières, Quebec, G8Z 4M3, Canada
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