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Acupuncture for Back and Neck Pain in an Emergency Room Setting

Efficacy of an Integrative Approach Utilizing Acupuncture as an add-on Therapy for the Treatment of Back and Neck Pain in an Emergency Department Setting - A Comparative Randomized Controlled Trial

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00859365
Acronym
ABNP
Enrollment
65
Registered
2009-03-11
Start date
2009-01-31
Completion date
2011-09-30
Last updated
2012-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Back Pain, Neck Pain, Range of Motion

Keywords

back pain, neck pain, anxiety, range of motion

Brief summary

This study aims to examine the efficacy of an Integrative approach utilizing Acupuncture as an add-on therapy for the treatment back and neck pain in an emergency department setting Acupuncture is well established as an effective treatment for back pain. The investigators cumulative experience in Asaf Harofeh Medical Center has shown Acupuncture to be an Effective therapy for simple back and neck pain in an ER setting. This study will examine weather Acupuncture can decrease pain, increase range of motion and decrease anxiety in patients admitted to the Emergency Room with simple back and neck pain without neurological findings. Acupuncture will be performed as an add on therapy on top of analgesic therapy.

Interventions

Real acupuncture treatment in real acupuncture points

PROCEDUREPlacebo Acupuncture

empty plastic acupuncture guide-tube located on the patients back in a non visable area and connected to a visible electric stimulator

PROCEDURENo intervention

Patients lay down for a period of 35 minutes without any treatment o intervention

Sponsors

Assaf-Harofeh Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Adult male and females age 18-60 with acute or sub acute/chronic simple back or neck pain * Agreed to a physical examination and by an orthopedic physician and X-ray * Diagnosis of simple back pain with levels of 4\<NRS at least * Agreed and able to fill pain, anxiety and satisfactory questioners * Agreed and able to sign informed consent

Exclusion criteria

* Fracture, sprain or neurological deficit during physical examination * Pain scale of NRS\< 4 * Referred or radiating pain * Active pregnancy * Active inflammatory arthritis * History of CVA * Open wounds * Acute malignancy with life expectancy of less than 5 years * Experience with acupuncture treatments * History of drug addiction * History of osteoporosis * Declined or unable to sign informed consent * Soldiers in active military service

Design outcomes

Primary

MeasureTime frame
A comparable difference in pain levels between a combined medication and acupuncture treatment to medication treatment alone as measured by the Numeric Rating Scale (NRS)At day of treatment, after 24 hrs

Secondary

MeasureTime frame
4.2.1 A comparable difference in range of motion between a combined medication and acupuncture treatment to medication treatment alone as measured by Spine Scan Device and physical exam using gonoimeterday of treatment, after 24 hrs
4.2.2 A comparable difference in patient self reported anxiety assessed by Hebrew version of the anxiety and somatization sections of the Symptom Check List-90 questioner (SCL-90)day of treatment
4.2.3 A comparable difference in the amount of analgesic pain medication consumed by the patients during the week following the treatmentday of treatment and after 24 hours
4.2.4 A comparable difference in safety and patient satisfactory as measured by overall satisfactory and safety questionnairesday of treatment, after 1 weekl

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026