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)
Numeric Pain Rating Scale (NPRS) — Baseline, to complete the treatments, on average 2 weeks, 1, 3 and 12 months after the end of treatment Numeric Pain Rating Scale (NPRS) The NPRS will be used to ask the patient about the level of pain that he/she feels considering from 0 to 10, where 0 represents the absence of pain and 10 represents the most intense pain, used to measure the pain experienced by the patient. The participant will answer the NPRS, responding to the average, maximum and minimum pain experienced throughout its duration.
Trial sites (1)
Facility
City
Region
Status
Rehasport Wroclaw
Wroclaw
Lower Silesian Voivodeship
More Wroclaw University of Health and Sport Sciences trials in Poland
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.
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