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Clinical Trials in Poland / NCT06975345
Starting soon Not applicable

Effects of a Protocol of Hip Flexor Stretching on Chronic Mechanical, Non-specific LBP.

NCT06975345 · tracked via the Priya Life Science Poland tracker
Phase
Not applicable
Started
2025-07-02
Last updated
2025-05-16

Condition(s) studied

PainMusculoskeletal ManipulationsLow Back Pain, Mechanical

Investigational drug(s) / intervention(s)

Multicomponent intervention. Hip flexors stretching, Strengthening exercises and education and medical treatment (Medication and medical counselling)Medical treatment.

Multicomponent intervention. Hip flexors stretching, Strengthening exercises and education and medical treatment (Medication and medical counselling): Hip flexors stretching (Adaptation from Evjenth and Hamberg) Strengthening Exercise * Deep squats * Flexo-extension of the ankle on a step over the head of metatarsal bones * Plank * Strengthening knee flexors and hip extensors * Lunges with a stick behind the patient back Education Pain relieving positions identified will be taught to the patient to use when they feel their pain. Identifying and learning to avoid pain positions or activities that increase pain. When the pain occur self stretching of hip flexors on the couch or the chair must be done

Medical treatment.: A medical doctor will prescribe the treatment following the standard of care in Polish public health services. Treatment will consist of medication and counseling.

Study summary

The goal of this clinical trial is to compare the effectiveness of a stretching, exercise and education protocol versus usual care in improving pain, function and disability in patients with non-specific mechanical chronic low back pain (CLBP). The research hypothesis is: A combination of hip flexors stretching, exercise and education is more effective than usual care to improve pain, function and disability in patients with CLBP.

Participants will be randomly allocated in one of the two treatment groups. Pain, function and disability will be assessed before starting treatment, after the end of the treatment and one month , three months and one year after the end of the treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
No
Inclusion Criteria: * Age 18-75 years * Medical diagnosis of chronic, mechanical, non-specific pain in the lumbar spine (M54, M51) - chronic low back pain. * Obtaining written consent to conduct research * Must be able to swallow tablets Exclusion Criteria: * Pregnancy * Pacemaker * Active cancer * To consent to conduct research * Difficulty communicating * The presence of a metal plate in the head and metal screws in the body * Condition after operations in the area of the lumbar spine * Condition after fractures in the lumbar spine * Contraindications to manual therapy or exercise * Has participated in a lumbar spine exercise or manual therapy program in the last three months * Present clear signs of having suffered a significant lumbar injury * Inability to maintain standing or a supine or prone position * No possibility to perform the stretching of hip flexors

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Rehasport Wroclaw Wroclaw Lower Silesian Voivodeship

More Wroclaw University of Health and Sport Sciences trials in Poland

Other trials for the same condition

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 NCT06975345 on ClinicalTrials.gov ↗ ← All trials in Poland