chronic nonspecific low back pain
Conditions
Interventions
Subjects and Methods: Of our hospital 65 years of age or older of low back pain patients who are attending to, be diagnosed by chronic low back pain and the doctor followed the onset more than three m
s maximum measured value in the same instrument. Every 5 seconds to put the force and loosen repeatedly, it continued for 10 minutes per set. Conducted a total of two sets, it is recorded in the diary
Sponsors
Department of Orthopaedic Surgery, Kanazawa University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: The subjects must meet all of the following criteria 1)Patient age at the time of obtaining informed consent is a full 65 years of age or older. 2)Patients from more than three months followed by chronic low back pain and a doctor from the onset received a diagnosis. 3)Patients who showed in the Numerical Rating Scale (NRS) related to low back pain, three or more of the value before the start of the study. 4)Patients after receiving a sufficient explanation Upon this test participation, on a sufficient understanding, the document agreed by the free will of the patient himself was obtained. 5)Out patient. 6)Patients physical therapist of this Institute study responsibility (shared) and a good command without problems the training to do for the study deems
Exclusion criteria
Exclusion criteria: Patients conflict with one of the following shall be not be incorporated in the study 1)Have heart disease, kidney disease, respiratory disease, blood disease, coagulation disorders and other serious complications, the patient is determined to be inappropriate by the attending physician. 2)The patient is poor understanding of the study due to dementia. 3)Patients with severe neurological symptoms, such as paralysis. 4)Patients with spinal surgical history 5)Patients with a diagnosis by a doctor as having specific lower back pain. 6)Patients with rheumatoid arthritis 7)Patients with a high degree of osteoporosis (such as fragility fracture history). 8)Other, patient research responsibility (sharing) who is determined to be unsuitable as a subject.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The number of expression adverse events, side effects after the start of treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement rate of low back pain NRS after enforcement treatment for 12 weeks. Analgesic use number of times change, JOABPEQ improvement rate, RDQ improvement rate, the amount of change in the trunk muscle strength measurements using an equivalent instrument, locomotive syndrome degree of improvement rate, changes in the eye-opening piece stepladder position time. | — |
Countries
Japan
Contacts
Public ContactNaoki Takahashi
Kanazawa University Hospital Orthopaedic Surgery
Outcome results
None listed