Actively Recruiting
Comparison of the Immediate Effect of Passive vs. Passive-Active Hamstring Stretching on Flexibility in Patients With Chronic Low Back Pain
Led by University Hospital, Clermont-Ferrand · Updated on 2025-11-25
90
Participants Needed
2
Research Sites
130 weeks
Total Duration
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AI-Summary
What this Trial Is About
The goal of this clinical trial is to determine whether a combination of passive and active hamstring stretching (PAS) is more effective than passive stretching alone (PS) in improving flexibility in patients with chronic low back pain (CLBP). The main questions it aims to answer are: Does PAS lead to greater improvements in active flexibility compared to PS? Does PAS provide additional benefits in passive flexibility, hamstring stiffness, and pelvic tilt? Researchers will compare the PAS group and the PS group to see if combining passive and active stretching results in greater improvements in flexibility and movement control. Participants will: Perform either PAS or PS stretching exercises as assigned. Undergo measurements of flexibility, hamstring stiffness, and pelvic tilt before and after the intervention. Answer a question about their perceived change in flexibility following the intervention. This study aims to improve rehabilitation strategies for people with CLBP, helping them achieve better movement and pain relief.
CONDITIONS
Official Title
Comparison of the Immediate Effect of Passive vs. Passive-Active Hamstring Stretching on Flexibility in Patients With Chronic Low Back Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female patients aged between 18 and 65 years
- Low back pain lasting at least 3 months
- Hamstring flexibility deficit shown by Straight Leg Raise less than 85 degrees
- Fingertip-to-Floor distance greater than 5 cm
You will not qualify if you...
- Presence of radicular pain
- Disc inflammation (MODIC Type 1)
- Neurological, cardiovascular, respiratory, or cancer-related diseases
- History of significant surgery such as lumbar fusion or joint replacements
- Pregnancy or breastfeeding
- Under protective legal measures
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Clermont Ferrand Univbersity HOspital, Louise Michel site
Cébazat, France, France, 63118
Actively Recruiting
2
CHU de Clermont-Ferrand
Clermont-Ferrand, France, 63000
Actively Recruiting
Research Team
L
Lise Laclautre
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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