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

U

Universität Duisburg-Essen

Status

Completed

Conditions

Mechanical/Motor Problems With Neck and Trunk
Neck Pain

Treatments

Procedure: Cupping massage

Study type

Interventional

Funder types

Other

Identifiers

NCT02651766
09-3987-BO

Details and patient eligibility

About

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.

Full description

see above

Enrollment

50 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Waiting List control group
No Intervention group
Description:
No treatment within the study period, were allowed to continue physiotherapy and medication. Were offered the treatment after finishing the study
Cupping massage treatment
Experimental group
Description:
Received the 5 cupping treatments, application twice a week on the upper back and neck
Treatment:
Procedure: Cupping massage

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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