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The Effects of Cupping Massage in Patients With Chronic Neck Pain - A Randomized Controlled Trial

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02651766
Acronym
SKM
Enrollment
50
Registered
2016-01-11
Start date
2009-05-31
Completion date
2011-02-28
Last updated
2018-05-02

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

Conditions

Neck Pain, Mechanical/Motor Problems With Neck and Trunk

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

Interventions

Using suction on the skin by means of glass cups, and moving the cups after applying massage oil on the skin

Sponsors

Universität Duisburg-Essen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain intensity3 weeks100mm Visual Analogue Scale from 0mm 'no pain' to 100mm 'maximal pain'

Secondary

MeasureTime frameDescription
Neck disability index3 weeksNDI measures neck pain complaints (Vernon und Mior 1991)
Quality of Life SF-363 weeksthe sf-36 is a short form health survey consisting of 8 scales to measure functional health and wellbeing (Bullinger & Kirchberger 1998)
mechanical detection threshold MDT3 weeksby von Frey filaments to measure perception threshold for light touch (Rolke, Pain, 2006)
Pain on movement (POM)3 weeks100mm Visual Analogue Scale from 0mm 'no pain' to 100mm 'maximal pain' Intensity rated for 6 movement directions flexion, tension, and rotation
pressure pain threshold PPT3 weekswith a pressure gauge algometer to determine threshold for painful pressure (Rolke, Pain, 2006) on the area of maximal neck pain, the adjacent and hand and foot
Adverse events3 weeksNumber of patients with adverse events
two point discrimination threshold3 weeksusing a pair of circles, determining the distance necessary between those to perceive them as separate sensations
vibration detection threshold VDT3 weekswith a tuning fork to measure perception threshold for vibration (Rolke, Pain, 2006)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026