Actively Recruiting
Comparison of Walking Using a Wearable Gait Analysis System in Patients Undergoing Lumbar Spinal Stenosis Surgery
Led by Pamukkale University · Updated on 2025-05-01
48
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Lumbar spinal stenosis (LSS) is a condition where the spinal canal narrows, compressing nerves and causing back and leg pain, weakness, and walking difficulties. It mainly affects people over 50, with symptoms worsening during walking or standing due to nerve compression. This study compares walking patterns between patients who have undergone LSS surgery and healthy individuals to better understand the impact of LSS on gait. Participants include those who had LSS surgery between 6 weeks and 3 months prior and healthy controls. Researchers will assess disability, pain, quality of life, and walking ability using tools like the Oswestry Disability Index, Visual Analog Scale for pain, SF-12 quality of life questionnaire, a 10-meter walk test, and a wearable gait analysis system called BTS G-Walk. During the study, participants will complete questionnaires and perform a walking test while wearing the gait analysis device to measure walking speed, step length, and gait patterns. The data collected will help evaluate differences in gait between LSS patients and healthy people. The study may last up to 3 months post-surgery for patients, with assessments taking about 30 minutes per participant.
CONDITIONS
Brief Title
Gait Assessment in Lumbar Spinal Stenosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Between the ages of 20 and 65
- Discharged from hospital after lumbar spinal stenosis surgery
- Surgery performed at least 6 weeks and at most 3 months ago
- No other orthopedic or neurological problems
- Able to communicate
- Agree to participate in the study
You will not qualify if you...
- Cognitive impairment
- Other neurological, psychiatric, or orthopedic problems besides lumbar spinal stenosis
- Medically unstable condition
- Open wounds, circulatory problems, or skin lesions in the area to be treated
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single assessment session
Participants complete assessments including disability status, pain level, quality of life, and gait parameters using the 10 Meter Walk Test and BTS G-Walk gait analysis system.
1 visit (in-person)
Duration - 6 weeks to 3 months
Participants are observed after surgery to monitor recovery and gait performance over time.
Trial Site Locations
Total: 1 location
1
Pamukkale University
Denizli, Turkey (Türkiye)
Actively Recruiting
Research Team
F
Fatma ÖZ
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Similar Trials
Frequently Asked Questions
Have more questions? Get in touch with our team for quick support
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here