DRKS00008319CompletedNot Applicable
Osteopathic treatment in patients with chronic muskuloskelettal disorders - an observational study
Institut für Sozialmedizin, Epidemiologie und Gesundheitsökonomie, Charité Universitätsmedizin Berlin0 sites40 target enrollmentStarted: May 28, 2015Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 40
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 30 Years to 65 Years (—)
- Sex
- All
Inclusion Criteria
- •30 to 65 years of age, female or male
- •- clinical diagnosis „chronic neck pain i.e. neck pain for at least 12 weeks, „chronic low back pain i.e. low back pain for at least 12 weeks, „chronic shoulder pain i.e. shoulder pain for at least 12 weeks, „chronic knee pain i.e. knee pain for at least 12 weeks
- •- intensity of the average muskuloskelettal pain over the last 7 days had to be more than 40 mm on a 100-mm visual analogue scale (VAS)
- •- willingness to get 6 osteopathic treatments within the next 6 month
- •- ability to give oral and signed written informed consent
- •- written informed consent
Exclusion Criteria
- •- osteopathic treatment within the last 12 month before beginn of study
- •- neck pain, low back pain, shoulder pain or knee pain caused by a malignant disease, infection or recent trauma
- •- kwown or suspected primary or secundary bone tumor
- •- known vascular anomaly such as aneurysm
- •- peripher or central neurological symptoms
- •- rheumatic diseases
- •- Joint replacements or other implants in the region of treatment
- •- obesity with BMI >30 Kg/m2
- •- intake of centrally acting analgesics
- •- pregnancy or breast feeding
- •- severe acute and or chronic disease which does not allow participation in the therapy
- •- other limitations which do not allow participation in the therapy
- •- alcohol or substance abuse
- •- no sufficient knowledge of German language
- •- current application for a benefit
- •- participation in another clinical trial during six months before the study and parallel to the study
- •- absence of written informed consent
Investigators
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