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Clinical Trials/NCT02258672
NCT02258672
Completed
N/A

Effects of a Preoperative Rehabilitation Program on the Recovery of Patients Undergoing Surgery for Lumbar Spinal Stenosis: a Feasibility Study.

Université du Québec à Trois-Rivières1 site in 1 country68 target enrollmentOctober 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Lumbar Spinal Stenosis
Sponsor
Université du Québec à Trois-Rivières
Enrollment
68
Locations
1
Primary Endpoint
Change from Baseline in disability
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of the present study is to evaluate the effectiveness of a prehabilitation program on the recovery of patients undergoing a minimally invasive surgery for degenerative lumbar spinal stenosis. To do so, 40 participants will be recruited and randomized into two groups; intervention or control group. Participants in the intervention group will take part in a physical training program, three times a week for six weeks before undergoing surgery. The exercise program will be supervised and will aim at improving core muscles strength and endurance as well as spine stability. It is hypothesized that the prehabilitation program will significantly improve disability and pain intensity reported by patients after surgery. Ultimately, this study aims to improve health care of patients awaiting lumbar surgery but its results may also impact the management of patients awaiting spine surgery for various conditions.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
March 1, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Martin Descarreaux

DC, PhD

Université du Québec à Trois-Rivières

Eligibility Criteria

Inclusion Criteria

  • To be affected by degenerative lumbar spinal stenosis and to be awaiting minimally invasive surgery for the lumbar spinal stenosis

Exclusion Criteria

  • Non-degenerative spinal stenosis, arthritic conditions (except for facet arthrosis), impaired cognitive function, spinal instability and disagreement from the treating neurosurgeon for the patient to take part in the preadaptation programme.

Outcomes

Primary Outcomes

Change from Baseline in disability

Time Frame: baseline, week 6, week 10, week 18, week 30

Oswestry Disability Index

Secondary Outcomes

  • Change from Baseline in pain intensity(baseline, week 6, week 10, week 18, week 30)

Study Sites (1)

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