CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 37 enrolled
Drug / intervention
Prehab for LSS +1 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05073081
NCT05073081N/ACompleted

Feasibility Testing of a Pre-surgical Rehabilitation (Prehab) Program for Patients With Lumbar Spinal Stenosis: a Pilot Randomized Controlled Trial

McMaster University·interventional·Posted Oct 11, 2021·Updated Nov 20, 2024

In Brief

A clinical study evaluating Prehab for LSS and Usual Care for Lumbar Spinal Stenosis and Prehabilitation. Completed, enrolled 37 participants across 4 sites.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

N/ACompletedFinished
20222023202420252026
First PostedOct 11, 2021
Enrollment StartDec 1, 2021
Primary CompletionSep 30, 2024
TodayJul 1, 2026
Enrollment to primary: 2.8 yearsPosted 4.7 years ago

Interventions

Prehab for LSSother

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.

Usual Careother

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