Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06888895

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

On this page

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered 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

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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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