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Walking Program for Lumbar Spinal Stenosis

N/A
Waitlist Available
Led By Michael Johnson, MD
Research Sponsored by University of Manitoba
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Subjects will be between the ages of 18 and 90
All LSS patients will demonstrate intractable neurogenic claudication and radiographically confirmed lumbar spinal stenosis
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 week x 4
Awards & highlights

Study Summary

This trial will test whether a walking program can improve the quality of life and functional status of patients with Lumbar Spinal Stenosis, post-surgery.

Who is the study for?
This trial is for adults aged 18-90 who have had surgery for lumbar spinal stenosis and are experiencing persistent leg pain or discomfort. They must not have had previous spine surgeries, significant other health issues like heart or nerve diseases, or physical injuries that would stop them from walking regularly.Check my eligibility
What is being tested?
The study tests a walking program's effectiveness on life quality and function in post-surgery lumbar spinal stenosis patients. Participants will start the program at either 2 or 3 months after surgery to compare improvements using pain scales, disability questionnaires, activity tracking devices, and step counts.See study design
What are the potential side effects?
Since this trial involves a walking program as an intervention rather than medication, side effects may include typical exercise-related responses such as muscle soreness or fatigue but should be minimal.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am between 18 and 90 years old.
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I have severe leg pain due to a confirmed narrowing of the spinal canal in my lower back.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 week x 4
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 week x 4 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Physical Activity Monitor

Trial Design

2Treatment groups
Active Control
Group I: Second group walkingActive Control1 Intervention
Group walking at 3 months postop
Group II: First walking groupActive Control1 Intervention
Group walking at 2 months postop

Find a Location

Who is running the clinical trial?

University of ManitobaLead Sponsor
595 Previous Clinical Trials
199,472 Total Patients Enrolled
Michael Johnson, MDPrincipal InvestigatorUniversity of Manitoba
2 Previous Clinical Trials
50 Total Patients Enrolled

Media Library

Walking program Clinical Trial Eligibility Overview. Trial Name: NCT00958490 — N/A
Lumbar Spinal Stenosis Research Study Groups: Second group walking, First walking group
Lumbar Spinal Stenosis Clinical Trial 2023: Walking program Highlights & Side Effects. Trial Name: NCT00958490 — N/A
Walking program 2023 Treatment Timeline for Medical Study. Trial Name: NCT00958490 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any remaining vacancies for participants in this clinical trial?

"This study is not currently recruiting, as the most recent edit to its information was made on August 13th 2011. However, there are an abundance of other clinical trials that are seeking participants at this time; 258 in total."

Answered by AI

Does the study sample extend to those aged 55 and above?

"This medical study is open to all adults age 18-90 years old. For those below the legal voting age, there are 21 other trials available and for seniors over 65, 252 studies exist."

Answered by AI

Is it permissible for me to join this experiment?

"This medical trial seeks to enroll 50 patients aged 18-90 with a pathological constriction. Furthermore, this trial will recruit both genders and must adhere to the age requirements of 18-90 years old."

Answered by AI
~3 spots leftby Apr 2025