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Acupuncture in Acute Nonspecific Low Back Pain

Acupuncture in Acute Nonspecific Low Back Pain; a Randomized Controlled Multicenter Study in General Practice

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01439412
Acronym
Acuback
Enrollment
185
Registered
2011-09-23
Start date
2014-03-17
Completion date
2018-03-17
Last updated
2024-02-09

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

Conditions

Low Back Pain

Keywords

Low back pain, Acupuncture, General practice

Brief summary

Acute low back pain is a common disorder in general practice. Some general practitioners (GPs) treat acute low back pain (LBP) with acupuncture, despite lacking evidence of its effectiveness for this condition. The aim of this study is to evaluate whether a single treatment-session with acupuncture can reduce time to recovery when applied in addition to standard LBP-treatment according to the Norwegian national guidelines. Analyses of prognostic factors for recovery and cost-effectiveness will also be carried out. The investigators hypotheses are: 1. Acupuncture treatment contributes to faster pain-recovery in acute LBP compared to standard treatment in general practice provided in accordance with the Norwegian national guidelines. 2. Acupuncture treatment for acute LBP improves function, and reduces drug use and sick leave, compared to the standard treatment in general practice provided in accordance with national guidelines. 3. Acupuncture treatment for acute LBP is a cost-effective treatment in general practice. The investigators intend to include a total of 270 patients, 135 in the intervention group and 135 in the control group. The investigators planned to do an interim analysis when reaching inclusion of 150 patients. However, this might lead to reduced overall significance level, and as a result of slow inclusion rate (by December 2015), the investigators plan to extend the inclusion time with one year and then complete the study in March 2017.

Interventions

PROCEDUREAcupuncture and standard treatment

This group will get standard treatment in general practice in accordance with national guidelines, i.e. general advice about activity, prescription of pain relievers (paracetamol, eventually ibuprofen and eventually tramadol), and eventually sick leave. In addition they also will receive one treatment of standardized acupuncture procedure during the consultation. The acupuncture treatment starts with distal points in the right hand: Lumbar Pain Points (Yaotongxue), strong stimulation for one minute. With the needles still positioned, the patient is instructed to make cautious back and hip movements in 2 minutes. Then the patient lies down on a bench to treat the local points Huatuojiaji (Jiaji) bilaterally in the segments of the L2-L4 for 5 minutes.

OTHERStandard treatment in general practice

This group will get standard treatment in general practice in accordance with national guidelines, i.e. general advice about activity, prescription of pain relievers (paracetamol, eventually ibuprofen and eventually tramadol), and eventually sick leave.

Sponsors

University of Oslo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Adults (20-55 years) who contact their general practitioners office because of acute nonspecific low back pain (0-14 days).

Exclusion criteria

* Nerve root affection and/or radiating pain below the knee. * Low back pain with suspected red flags, i.e. infections, tumors and metastatic disease, rheumatic disease, fractures and significant deformities of the spine. * Low back pain which starts in pregnancy. * Physician reported sick leave of 14 days or more during the last month before the back pain, for any reason.

Design outcomes

Primary

MeasureTime frameDescription
Median time in days to recovery of pain.1 yearThe median time in days to recovery of pain is measured at the first day the patient scores 0 or 1 point on the Numerical Rating Scale (NRS).

Secondary

MeasureTime frameDescription
Global measure of improvement1 yearMeasuring the patients perception of change, stated in whole numbers from 1 = much better to 5 = much worse (Likert improvement scale).
Back specific functional status1 yearMeasuring patients' perception of function. The patient answers yes or no concerning 24 allegations about the activities and condition, depending on whether they feel that the statement describes them on this day. Roland Morris Disability Questionnaire.
Sick leaves1 yearThe number of days away from work due to back pain.
Reduction in pain1 yearPain as measured by the Numeric Rating Scale (NRS), before and immediately after treatment and at the other follow-up times.
Visits at the GP1 yearNumber of new visits at the GP for the back pain.
Side effects of treatment1 yearReporting of possible side effects of the treatment, both acupuncture and medication.
Use of medication1 yearUse of medication. Paracetamol, eventually others. Counting of daily consumption.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026