Klinik für Naturheilkunde
Essen, Germany
NCT Number: NCT01500330
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.
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Notify Me18 year–75 year
All sexes
Interventional
Not applicable
Essen, Germany
see above
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
the upper back is covered in massage oil the cupping glass is drawn along the back muscles
standardized programme on muscle relaxation according to Jacobson
Time frame: T2 (84 days)
Pain intensity on a 100mm visual analogue scale
Time frame: week 12
Pain intensity on a visual analogue scale
Time frame: T2 (84 days)
Pain intensity induced by flexion, extension, lateral flexion and rotation of the head
Time frame: T2 (84 days)
sensory and affective pain quality, questionnaire
Time frame: T2 (84 days)
Well being measured by questionnaire (FEW16)
Time frame: T2 (84 days)
measured by the SF-36
Time frame: T2 (84 days)
Measured by the PSQ20
Time frame: T2 (84 days)
measured by the GKÜ (questionnaire on control beliefs)
Time frame: T2 (84 days)
pressure pain threshold measured with an algometer on predefined muscles and the pain maximum
Time frame: T2(84 days)
all adverse events are recorded
Universität Duisburg-Essen
Other
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]
Acronym: NaSK
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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