Preoperative Rehabilitation for Patients Undergoing Surgery for Lumbar Spinal Stenosis

NCT ID: NCT02258672

Last Updated: 2020-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

68 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-10-31

Study Completion Date

2020-03-01

Brief Summary

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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.

Detailed Description

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Conditions

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Lumbar Spinal Stenosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Prehabilitation program

Participants will be physically trained before undergoing surgery

Group Type EXPERIMENTAL

Prehabilitation program

Intervention Type OTHER

Progressive and individualized physical training aimed at improving core muscles strength and endurance as well as spinal stability.

Control

Patients will follow the normal course of care provided by the hospital

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Prehabilitation program

Progressive and individualized physical training aimed at improving core muscles strength and endurance as well as spinal stability.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fonds de soutien au démarrage de projets en collaboration (CSSSTR)

UNKNOWN

Sponsor Role collaborator

Fonds pour la Recherche Clinique de l'UQTR

UNKNOWN

Sponsor Role collaborator

Université du Québec à Trois-Rivières

OTHER

Sponsor Role lead

Responsible Party

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Martin Descarreaux

DC, PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Martin Descarreaux, DC, PhD

Role: STUDY_DIRECTOR

Université du Québec à Trois-Rivières

Locations

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Université du Québec à Trois-Rivières

Trois-Rivières, Quebec, Canada

Site Status

Countries

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Canada

References

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Marchand AA, Suitner M, O'Shaughnessy J, Chatillon CE, Cantin V, Descarreaux M. Effects of a prehabilitation program on patients' recovery following spinal stenosis surgery: study protocol for a randomized controlled trial. Trials. 2015 Oct 27;16:483. doi: 10.1186/s13063-015-1009-2.

Reference Type DERIVED
PMID: 26507388 (View on PubMed)

Other Identifiers

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UQTR-CSSSTR 2014

Identifier Type: -

Identifier Source: org_study_id

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