Skip to content

Home Use of Cupping Massage in Chronic Neck Pain

Randomised Controlled Study on the Effectiveness of Cupping Massage for Home Use in Chronic Neck Pain [Randomisierte Kontrollierte Studie Zur Wirksamkeit Der Schröpfkopfmassage Als Heimanwendung Bei Chronischen Nackenschmerzen]

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01500330
Acronym
NaSK
Enrollment
84
Registered
2011-12-28
Start date
2012-01-31
Completion date
2012-05-31
Last updated
2013-10-09

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

Conditions

Neck Pain

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

Interventions

the upper back is covered in massage oil the cupping glass is drawn along the back muscles

PROCEDUREProgressive muscle relaxation

standardized programme on muscle relaxation according to Jacobson

Sponsors

Universität Duisburg-Essen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

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

Design outcomes

Primary

MeasureTime frameDescription
Pain IntensityT2 (84 days)Pain intensity on a 100mm visual analogue scale

Secondary

MeasureTime frameDescription
pain intensity in motionT2 (84 days)Pain intensity induced by flexion, extension, lateral flexion and rotation of the head
pain qualityT2 (84 days)sensory and affective pain quality, questionnaire
well beingT2 (84 days)Well being measured by questionnaire (FEW16)
Quality of lifeT2 (84 days)measured by the SF-36
Pain diaryweek 12Pain intensity on a visual analogue scale
Control beliefT2 (84 days)measured by the GKÜ (questionnaire on control beliefs)
Pressure pain thresholdT2 (84 days)pressure pain threshold measured with an algometer on predefined muscles and the pain maximum
SafetyT2(84 days)all adverse events are recorded
Stress perceptionT2 (84 days)Measured by the PSQ20

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026