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Home Use of Cupping Massage in Chronic Neck Pain

Not Applicable
Completed
Conditions
Neck Pain
Interventions
Procedure: Progressive muscle relaxation
Procedure: cupping massage
Registration Number
NCT01500330
Lead Sponsor
Universität Duisburg-Essen
Brief Summary

The purpose of this randomized controlled study is to determine the effectiveness of cupping massage as home use for patients with chronic nonspecific neck pain compared to relaxation exercise.

Detailed Description

see above

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
84
Inclusion Criteria
  • mean neck pain intensity 45mm
  • neck pain for at least 3 months
  • age 18-75
  • partner or friend for the application of the massage
Exclusion Criteria
  • specific neck pain due to trauma, neurological disorder, prolapse, operation, cancer
  • severe deformity of the spine
  • skin disease, allergy on the neck area
  • hemophilia, anticoagulation, antiplatelet disorder
  • severe psychiatric disorder
  • severe comorbidity
  • regular intake of opiates and corticosteroids >10mg prednisolon
  • pregnancy
  • participation in other clinical trials

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
control groupProgressive muscle relaxationprogressive muscle relaxation twice a week for 20 minutes
cupping massagecupping massage12 weeks home use of cupping massage (delivered by the partner or friend) twice a week for 20 minutes
Primary Outcome Measures
NameTimeMethod
Pain IntensityT2 (84 days)

Pain intensity on a 100mm visual analogue scale

Secondary Outcome Measures
NameTimeMethod
pain intensity in motionT2 (84 days)

Pain intensity induced by flexion, extension, lateral flexion and rotation of the head

Quality of lifeT2 (84 days)

measured by the SF-36

well beingT2 (84 days)

Well being measured by questionnaire (FEW16)

Stress perceptionT2 (84 days)

Measured by the PSQ20

Control beliefT2 (84 days)

measured by the GKÜ (questionnaire on control beliefs)

Pain diaryweek 12

Pain intensity on a visual analogue scale

pain qualityT2 (84 days)

sensory and affective pain quality, questionnaire

SafetyT2(84 days)

all adverse events are recorded

Pressure pain thresholdT2 (84 days)

pressure pain threshold measured with an algometer on predefined muscles and the pain maximum

Trial Locations

Locations (1)

Klinik für Naturheilkunde

🇩🇪

Essen, Germany

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