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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01439412
Other study ID # Acuback
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 17, 2014
Est. completion date March 17, 2018

Study information

Verified date February 2024
Source University of Oslo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 185
Est. completion date March 17, 2018
Est. primary completion date March 17, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years to 55 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Acupuncture 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.
Other:
Standard 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.

Locations

Country Name City State
Norway Institute of Health and Society, Faculty of Medicine, University of Oslo Oslo

Sponsors (1)

Lead Sponsor Collaborator
University of Oslo

Country where clinical trial is conducted

Norway, 

References & Publications (2)

Skonnord T, Skjeie H, Brekke M, Grotle M, Lund I, Fetveit A. Acupuncture for acute non-specific low back pain: a protocol for a randomised, controlled multicentre intervention study in general practice--the Acuback Study. BMJ Open. 2012 Jun 25;2(3):e001164. doi: 10.1136/bmjopen-2012-001164. Print 2012. — View Citation

Skonnord T, Skjeie H, Brekke M, Klovning A, Grotle M, Aas E, Mdala I, Fetveit A. Acupuncture for acute non-specific low back pain: a randomised, controlled, multicentre intervention study in general practice-the Acuback study. BMJ Open. 2020 Aug 6;10(8):e034157. doi: 10.1136/bmjopen-2019-034157. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Median time in days to recovery of pain. The 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). 1 year
Secondary Reduction in pain Pain as measured by the Numeric Rating Scale (NRS), before and immediately after treatment and at the other follow-up times. 1 year
Secondary Global measure of improvement Measuring the patients perception of change, stated in whole numbers from 1 = much better to 5 = much worse (Likert improvement scale). 1 year
Secondary Back specific functional status Measuring 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. 1 year
Secondary Sick leaves The number of days away from work due to back pain. 1 year
Secondary Use of medication Use of medication. Paracetamol, eventually others. Counting of daily consumption. 1 year
Secondary Visits at the GP Number of new visits at the GP for the back pain. 1 year
Secondary Side effects of treatment Reporting of possible side effects of the treatment, both acupuncture and medication. 1 year
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