Safety evaluation of abdominal trunk muscle training for chronic low back pai

Not Applicable

• Conditions: chronic nonspecific low back pain

• Registration Number: JPRN-UMIN000023181
• Lead Sponsor: Department of Orthopaedic Surgery, Kanazawa University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-07-15
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

Not provided

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.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The number of expression adverse events, side effects after the start of treatment.

Secondary Outcome Measures

Name	Time	Method
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.