Randomised Controlled Trial on the Influence of Cupping Massage on Pain Intensity and Sensory Mechanical and Pain Thresholds in Patients With Chronic Non Specific Neck Pain
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Neck Pain
- Sponsor
- Universität Duisburg-Essen
- Enrollment
- 50
- Locations
- 1
- Primary Endpoint
- Pain intensity
- Status
- Completed
- Last Updated
- 8 years ago
Overview
Brief Summary
The study aims to investigate the influence of 5 cupping massage treatments on chronic non specific neck pain. 50 patients with neck pain are randomised into cupping treatment and waiting list control group. Before and after the intervention the investigators evaluate the neck pain (VAS), the neck related disability (NDI), pain on movement (POM) and the quality of life (SF36) and safety. To investigate neurophysiological effects of cupping the investigators also measure mechanical detection threshold (MDT), vibration detection threshold (VDT) and pressure pain threshold (PPT) and the two point discrimination threshold at pain related and control areas.
The treatment group receives 5 cupping treatments over a period of 3 weeks.
Detailed Description
see above
Investigators
Romy Lauche
Principle investigator
Universität Duisburg-Essen
Eligibility Criteria
Inclusion Criteria
- •age between 18 and 75
- •permanent neck pain for at least three months in a row
- •a minimum of 40mm of neck pain on a 100mm visual analogue scale (VAS)
Exclusion Criteria
- •neck pain caused by trauma, inflammatory or malignant disease, by congenital malformation of the spine or if pain was accompanied by radicular symptoms such as radiating pain, paresis, prickling or tingling.
- •invasive treatments within the last 4 weeks, surgery to the spine within the last year, corticosteroid or opioid treatment.
- •serious acute or chronic organic disease such as diabetes or cancer, mental disorders, pregnancy, and haemorrhagic tendency or anticoagulation treatment.
- •non steroidal pain medication and physiotherapy were allowed if the treatment regimen was not altered for four weeks before and continued during the study.
Outcomes
Primary Outcomes
Pain intensity
Time Frame: 3 weeks
100mm Visual Analogue Scale from 0mm 'no pain' to 100mm 'maximal pain'
Secondary Outcomes
- pressure pain threshold PPT(3 weeks)
- Adverse events(3 weeks)
- two point discrimination threshold(3 weeks)
- Pain on movement (POM)(3 weeks)
- Neck disability index(3 weeks)
- Quality of Life SF-36(3 weeks)
- mechanical detection threshold MDT(3 weeks)
- vibration detection threshold VDT(3 weeks)