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A Pilot Study Comparing Frequency and Style of Acupuncture for Chronic Low Back Pain
ISRCTN ISRCTN41571810
ClinicalTrials.gov identifier
Public title A Pilot Study Comparing Frequency and Style of Acupuncture for Chronic Low Back Pain
Scientific title
Acronym ACLBP
Serial number at source 1
Study hypothesis 1. To compare the effectiveness of traditional chinese acupuncture, based on traditional Chinese medical (TCM) diagnosis, with moxibustion/cupping if necessary, with Western acupuncture based on Western diagnosis, without moxibustion/cupping, for chronic non-specific chronic low back pain
2. To explore whether intensive acupuncture treatment frequencies i.e. 5 treatments/week can achieve better treatment effects than 2 treatments/week, for non-specific low back pain
Ethics approval Not provided at time of registration
Study design Randomised controlled trial
Countries of recruitment United Kingdom
Disease/condition/study domain Non-specific low back pain
Participants - inclusion criteria 1. Non-specific acute or chronic low back pain (LBP) as the chief complaint, with or without leg pain
2. Age between 18-60 years and of both genders
Participants - exclusion criteria 1. History of disc or spine surgery
2. Sciatica
3. Neurological disorders and possible serious pathological back problem
4. Systemic bone or joint disorders (e.g. rheumatoid arthritis)
5. Pregnancy
6. Dementia
7. Severe clotting disorders or anticoagulant therapy
8. Epilepsy
9. Systemic or visceral disease
10. Current use of systemic corticosteroids, muscle relaxants, narcotic medications
11. Overt psychiatric illness
12. Receiving acupuncture treatment within the past 6 months
13. Unemployment or having current pending compensation claims
14. Other acute orthopaedic or medical problems
Anticipated start date 01/09/2005
Anticipated end date 01/12/2005
Status of trial Completed
Patient information material
Target number of participants 40
Interventions 1. Traditional Chinese acupuncture (with moxibustion and cupping if necessary)
2. Western acupuncture
Primary outcome measure(s) Visual analogue scale (VAS)
Secondary outcome measure(s) 1. Functional disability
2. Quality of life
3. Psychological impact
4. Shuttle walk test
5. Lateral trunk flexibility
Sources of funding University of Ulster (UK) - Vice Chancellor Scholarship (VCRS)
Trial website
Publications
Contact name Prof  Suzanne  McDonough
  Address 14J15, Rehabilitation Sciences Research Institute
University of Ulster
Shore Road
Newtown Abbey
  City/town County Antrim
  Zip/Postcode BT37 0QB
  Country United Kingdom
  Tel +44 (0)28 90 366459
  Email S.McDonough@ulster.ac.uk
Sponsor University of Ulster (UK)
  Address Vice Chancellor Scholarship
Research office
University of Ulster
  City/town County Antrim
  Zip/Postcode BT37 0QB
  Country United Kingdom
  Email n.curry@ulster.ac.uk
Date applied 24/08/2005
Last edited 14/07/2010
Date ISRCTN assigned 04/11/2005
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