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Preoperative Rehabilitation for Patients Undergoing Surgery for Lumbar Spinal Stenosis

U

Université du Québec à Trois-Rivières

Status

Completed

Conditions

Lumbar Spinal Stenosis

Treatments

Other: Prehabilitation program

Study type

Interventional

Funder types

Other

Identifiers

NCT02258672
UQTR-CSSSTR 2014

Details and patient eligibility

About

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.

Enrollment

68 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

68 participants in 2 patient groups

Prehabilitation program
Experimental group
Description:
Participants will be physically trained before undergoing surgery
Treatment:
Other: Prehabilitation program
Control
No Intervention group
Description:
Patients will follow the normal course of care provided by the hospital

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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