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N/A N=80 Randomized Double-blind Treatment

Acupuncture Using Yamamoto's Method for the Treatment of Acute Nonspecific Low Back Pain

Low Back Pain

Enrolled (actual)
80
Serious AEs
0.0%
Results posted
Jun 2011
Primary outcome: Primary: Pain Assessed on a 10-point Numeric Pain Scale — 6.55; 6.68; 4.63; 5.13 cm

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Acupuncture (Other); Non-penetrating acupuncture (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Federal University of São Paulo
Primary completion
Jun 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Pain Assessed on a 10-point Numeric Pain Scale
6.55; 6.68; 4.63; 5.13; 3.83; 4.4
SECONDARY
Roland-Morris Disability Questionnaire (RM)
14.9; 14.6; 10.3; 12.4; 8.1; 10.2 0,05 sig
SECONDARY
Quality of Life Assessed on the SF-36
46.4; 55.8; 58.5; 60.6; 68.8; 66.6
SECONDARY
Likert Improvement Assessment Scale
1.6; 2.15; 1.6; 2.0; 1.67; 2.27
SECONDARY
Number of Anti-inflammatory Tablets Taken
1.5; 2.6; 1.9; 4.2; 1.3; 3.3

Summary

The aim of the present study is to assess the effectiveness of acupuncture using Yamamoto's method for the treatment of ANLBP using the following outcomes:pain,functional capacity,quality of life and number of 50 mg sodium diclofenac pills taken per day.

Eligibility Criteria

Inclusion Criteria

  • Male or female
  • Aged 18 to 65 years
  • Seeking medical assistance for nonspecific low-back pain
  • Score of 4 to 8 cm on the pain scale (0 to 10 cm)
  • Agreed to participate and signed term of informed consent

Exclusion Criteria

  • Patients with a diagnostic investigation of secondary causes as spondyloarthropathy, infection, tumor or fracture
  • Sciatica lumbar pain
  • Previous surgery on spinal column
  • Litigation
  • Having changed physical activity or underwent acupuncture or physical therapy in previous three months,
  • Having previously undergone scalp acupuncture
  • Pregnancy
  • Contraindication for anti-inflammatory agents
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01124955). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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