Motion Style Acupuncture Treatment for Low Back Pain With Severe Disability

Complete Immobility Due to Severe Physical Disability Clinical Trial

— MSAT  

Official title:

Motion Style Acupuncture Treatment for Low Back Pain With Severe Disability: a Randomised, Controlled, Trial Protocol

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01315561
• Other study ID #: JSR-2011-01
• Status: Completed
• Phase: Phase 3
• Start date: April 2011
• Est. completion date: April 2012

Study information

• Verified date: November 2018
• Source: Jaseng Hospital of Korean Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Motion style acupuncture treatment(MSAT) is a treatment method in which the patient is exposed to active or passive movement and exercise during acupuncture, as opposed to conventional acupuncture. The purpose of this study is to investigate the effect of MSAT in the treating pain and severe functional disability in acute LBP patients.

Description:

58 patients with acute LBP and severe disability with an Oswestry Disability Index(ODI) of 60% or higher were randomly allocated and divided into 2 groups. The experimental group was treated with MSAT and the control group was treated with intramuscular injections of diclofenac(NSAID). All administrations were limited to 1 session, and comparisons were made of measurements before and after treatment. Primary outcomes were measured by the NRS(numerical rating scale) of back pain in active movement. Secondary outcomes were measured by the NRS of radiating pain, ODI scores, and the patient's global impression of change(PGIC) etc. Post-treatment follow-up will be performed to measure primary and secondary outcomes with the exception of ROM and SLR at 2, 4, and 24 weeks after treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 58
• Est. completion date: April 2012
• Est. primary completion date: October 2011
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 60 Years

Eligibility

Inclusion Criteria:

• Acute LBP(with or without leg pain), with onset within past 4 weeks

• Severe disability as assessed by an Oswestry Disability Index of 60% or higher

• Age between 20 and 60

• Given consent to lumbar MRI

• Voluntary participation with written consent given to study consent form

Exclusion Criteria:

• Diagnosis of serious disease(s) which are possible causes of back pain such as malignancy, vertebral fracture, spinal infection, inflammatory spondylitis, cauda equina compression, etc.

• Prior diagnosis of other chronic disease(s) which could affect effectiveness or interpretation of treatment results such as cardiovascular disease, diabetic neuropathy, fibromyalgia, rheumatoid arthritis, Alzheimer's disease, epilepsy, etc.

• Progressive neurologic deficit(s) or concurrent severe neurological symptoms

• Unsuitable for or at risk of complications from acupuncture treatment such as patients with clotting disorders, severe diabetes with risk of infection, serious cardiovascular disease, or undergoing anticoagulant treatment, etc.

• Under prescription of corticosteroids, immuno-suppressant drugs, psychiatric medicine, or other medication considered unsuitable for subjects by the researcher

• Experience of gastroenteric complications after taking NSAIDs or currently undergoing treatment for digestive disorders

• During pregnancy or suspected pregnancy

• Subjects considered unsuitable for clinical trial by the researcher

Related Conditions & MeSH terms

• Back Pain
• Complete Immobility Due to Severe Physical Disability
• Low Back Pain

Intervention

Other:
• acupuncture, injection
MSAT and intramuscular injections of diclofenac(NSAID)

Locations

Country	Name	City	State
Korea, Republic of	Jaseng Oriental Hospital	Bucheon
Korea, Republic of	Jaseng Oriental Hospital	Seoul	Gangnamgu Sinsadong

Sponsors (1)

Lead Sponsor	Collaborator
Jaseng Hospital of Korean Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from Baseline in numerical rating scale of back pain		Before treatment, At 30 minutes, 2, 4, and 24 weeks after treatment.
Secondary	Change from Baseline in NRS of radiating pain, ODI scores, and the patient's global impression of change(PGIC),range of motion (ROM) of the lumbar spine, and degrees of straight leg raising (SLR)	Post-treatment follow-up will be performed to measure primary and secondary outcomes with the exception of ROM and SLR at 2, 4, and 24 weeks after treatment.	Before treatment, At 30 minutes, 2, 4, and 24 weeks after treatment.