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Feasibility of Prehab for Lumbar Spinal Stenosis

NCT05073081 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 37

Last updated 2024-11-20

No results posted yet for this study

Summary

The literature has shown evidence of the effectiveness of prehabilitation programs on post-operative recovery for musculoskeletal conditions; however, evidence for prehabilitation for lumbar spinal stenosis (LSS) is limited. Investigators have found that there is very low to low quality evidence for the effect of prehabilitation interventions for improving outcomes following lumbar spine surgery. Therefore, the purpose of this study will be to determine the feasibility of a prehabilitation program for patients undergoing LSS surgery, and pilot test the protocol to provide the foundation for future design of a larger, multicenter randomized controlled trial.

Conditions

  • Lumbar Spinal Stenosis
  • Prehabilitation

Interventions

OTHER

Prehab for LSS

The 8-week prehabilitation program will be delivered online by physiotherapists, chiropractors, and kinesiologists through synchronous and asynchronous exercise sessions, along with online educational sessions.

OTHER

Usual Care

Participants in the control group will receive usual care as per surgeons' current practice.

Sponsors & Collaborators

  • University of Calgary

    collaborator OTHER

  • University of Alberta

    collaborator OTHER

  • McMaster University

    lead OTHER

Principal Investigators

  • Luciana G Macedo, PhD · McMaster University

  • Doug Gross, PhD · University of Alberta

  • Lisa Carlesso, PhD · McMaster University

  • Kenneth Thomas, MD · University of Calgary

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-01
Primary Completion
2024-09-30
Completion
2024-09-30

Countries

  • Canada

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05073081 on ClinicalTrials.gov