Effectiveness of Diaphragm Treatment in Reducing Low Back Pain
Low Back Pain, Mechanical
About this trial
This is an interventional treatment trial for Low Back Pain, Mechanical focused on measuring low back pain, diaphragm, lumbar pain, physiotherapy, conventional, treatment
Eligibility Criteria
Inclusion Criteria: Patient diagnosed with subacute or chronic mechanical low back pain by a specialist doctor and who has attended in "Fisioclinic" physiotherapy clinic. Older than 18 years-old. Indistinct sex. Diaphragm dysfunction. Exclusion Criteria: Any surgical intervention on the upper and lower limbs, head, spine, thorax or abdomen at any time in their lives, with a visible anatomy cause on imaging tests. Any pathology of non-mechanical origin, such as inflammatory, infectious, tumorous, neurological, traumatic processes and bone diseases in the lumbar spine. Having received analgesic or anti-inflammatory medical treatment for pain in a period of less than two weeks. Pregnant women, including the breastfeeding period. Patients receiving chemotherapy or radiotherapy. Basic systemic disease of rheumatic origin (for example, arthritis, osteoarthritis, gout and psoriasis). Implanted electronic devices. Drug or alcohol abuse, analgesic or sedative therapy and use of medications that affect the central nervous system (for example, antidepressants, anxiolytics and anticonvulsants). Patients who have previous experience with manual treatment of the diaphragm. Patients with high work activity. Outside the age range for the study. Refusal to participate in the study. Refusal to complete and sign the informed consent.
Sites / Locations
- Juan Antonio Díaz-ManchaRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Diaphragm technique
conventional physiotherapy
The continuity between the diaphragm and the lumbar spine demonstrates the existence of an anatomical and functional connection between them. Changes in the mobility of the diaphragmatic domes in addition to improvement in spirometric parameters when carrying out a diaphragm stretching technique. This makes us think that the mobility of the lumbar spine may be compromised by diaphragm dysfunction.
Application of the tetrapolar transcutaneous electrical neurostimulation (TENS) device with the "I-tech Mio-care" equipment in the analgesia program with an intensity of between 10-20 milliamps, according to the patient's tolerance, with an application time of 15 minutes in the lumbar paravertebral area on both sides. 250w infrared lamp at a distance of 1m from the patient, with an application time of 10 minutes. Ultrasound on the quadratus lumborum muscle area with a frequency of 1Mhz, at an intensity of 1.2w/cm2 and with an application time of 10 minutes. Ischemic compression and analytical stretching of the quadratus lumborum, multifidus and iliocostalis muscles, constant pressure with the thumb on each muscular trigger point (MTrP) for between 30 s and 2 min the intensity of the pressure will be adjusted to a level at which each subject reports "comfortable pain", that is, between the pain threshold and the maximum tolerable pain