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Clinical Trials in Turkey / NCT07182825
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Effects of Multifidus Lift Exercise on Endurance, Pain, and Disability in University Students With Low Back Pain

NCT07182825 · tracked via the Priya Life Science Turkey tracker
Sponsor
Mehmet Akif Guler
Phase
Not applicable
Started
2025-10-01
Last updated
2025-09-19

Condition(s) studied

Low Back PainNon Specific Chronic Low Back PainHealthy Vollunteer

Investigational drug(s) / intervention(s)

Modified Multifidus Lift Exercise (MLE)

Modified Multifidus Lift Exercise (MLE): A supervised stabilization exercise protocol designed to selectively activate the lumbar multifidus muscle. In the quadruped position, the contralateral knee is maintained approximately 10 cm above the ground while the participant performs controlled trunk stabilization. Sessions are conducted twice weekly for 6 weeks, each including warm-up (5 minutes brisk walk, mobilization, hamstring stretch), the modified Multifidus Lift Exercise with progressive repetitions (weeks 1-2: 8-10, weeks 3-4: 10-12, weeks 5-6: 12-15), and cool-down (static stretches). All sessions are supervised to ensure correct form, breathing control, and safety.

Study summary

Nonspecific low back pain is a common musculoskeletal problem that also affects many young adults, including university students. It can negatively impact academic performance, daily life, and overall well-being. Research shows that stabilization exercises targeting the lumbar multifidus muscle play an important role in rehabilitation, but it is unclear whether modified versions of these exercises may provide additional benefits.

This study will investigate a simple modification of the traditional "bird-dog" exercise, called the "Multifidus Lift Exercise." In this version, participants maintain the contralateral knee about 10 cm above the ground while in a four-point kneeling position. This adjustment is expected to increase multifidus activation and improve back endurance.

University students aged 18-25 with nonspecific low back pain will participate in a 6-week supervised program, performing the exercise twice weekly. A healthy control group without low back pain will also be included. The main outcome will be back extensor muscle endurance (Biering-Sørensen Test). In participants with back pain, pain intensity (Visual Analog Scale) and functional disability (Oswestry Disability Index) will also be measured.

The study aims to determine whether this low-cost, practical, and time-efficient exercise can improve muscle endurance, reduce pain, and decrease disability in young adults with low back pain. Results may provide evidence for an effective and accessible preventive and therapeutic approach in student populations.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Age between 18 and 25 years Currently enrolled as a university student at Selçuk University Willing to participate voluntarily and sign informed consent form Medically suitable for exercise participation For NSCLBP group: History of nonspecific chronic low back pain within the past 3 months Physician confirmation of nonspecific low back pain Oswestry Disability Index (ODI) ≥ 21% (moderate disability) Visual Analog Scale (VAS) score ≥ 3.5 For Healthy control group: No history of low back pain within the past 3 months Physician confirmation of no contraindications for exercise Exclusion Criteria: * Presence of radicular pain or nerve root compression symptoms History of spinal surgery Neurological deficits within the past 3 months (e.g., muscle weakness, reflex loss, paresthesia) Systemic infection or systemic disease affecting participation Cardiovascular or pulmonary disease contraindicating exercise Clinical "red flag" symptoms (e.g., saddle anesthesia, bowel/bladder incontinence, fever, known cancer) Pregnancy Regular use of analgesics, muscle relaxants, or anti-inflammatory medications Participation in regular exercise programs in the past 3 months Active involvement in sports directly affecting lumbar muscles (e.g., fitness, pilates, yoga, swimming) Inability to comply with exercise sessions or study protocol

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Selçuk University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation Konya Konya

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07182825 on ClinicalTrials.gov ↗ ← All trials in Turkey