Assessing walking patterns in patients with lumbar spinal stenosis
Comparison of Walking With Wearable Gait Analysis System in Patients Undergoing Lumbar Spinal Stenosis Surgery
This study looks at how walking patterns change in people aged 20-65 who have had surgery for lumbar spinal stenosis to better understand their mobility after recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 48 (estimated) |
| Ages | 20 Years to 65 Years |
| Sex | All |
| Sponsor | Pamukkale University Academic / other |
| Locations | 1 site (Denizli) |
| Trial ID | NCT06750055 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on patients diagnosed with lumbar spinal stenosis, a condition characterized by the narrowing of the spinal canal that can lead to back pain and neurological issues. Participants aged 20-65 who have undergone surgery for this condition will be assessed for their gait patterns between 6 weeks and 3 months post-discharge. The study aims to gather data on how lumbar spinal stenosis affects walking and mobility, which could inform future treatment approaches. The research will exclude individuals with other orthopedic or neurological issues to ensure a focused analysis.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 20-65 who have recently undergone surgery for lumbar spinal stenosis and are in stable condition.
Not a fit: Patients with cognitive impairments or other significant orthopedic or neurological conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of gait abnormalities in lumbar spinal stenosis, leading to improved rehabilitation strategies.
How similar studies have performed: While there have been studies on gait in various conditions, this specific focus on lumbar spinal stenosis is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Between the ages of 20-65 and discharged from hospital, * At least 6 weeks and at most 3 months after surgery, * No other orthopedic and neurological problems, * Able to communicate, * Individuals who agree to participate in the study will be included in the study. Exclusion Criteria: * Cognitive impairment, * Other neurologic, psychiatric and/or orthopedic problems other than lumbar spinal stenosis, * Medically unstable, * Individuals with open wounds, circulatory problems, skin lesions in the area to be treated will be excluded from the study.
Where this trial is running
Denizli
- Pamukkale University — Denizli, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Fatma ÖZ
- Email: fatmaoz8499@gmail.com
- Phone: 5358510875
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.