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临床试验/DRKS00034310
DRKS00034310尚未招募Unknown

Effectiveness of osteopathic medicine in patients with chronic shoulder pain - A two-arm, randomized controlled, open-label, monocentric study - Osteopathic medicine in shoulder pain (Akronym: OsteoShoulder)

Charité - Universitätsmedizin Berlin, Institut für Sozialmedizin, Epidemiologie und Gesundheitsökonomie0 个研究点目标入组 66 人开始时间: 2024年5月21日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
66

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 65 Years(—)
性别
All

入选标准

  • Important inclusion criteria:
  • - Age from 18 to 65 years, any gender
  • - Clinical diagnosis of CSP (duration of disease at least 12 weeks, including bursitis sub-acromialis, tendinosis calcarea, frozen shoulder) on the most painful shoulder
  • - Subjectively perceived pain intensity at the most painful shoulder within the last seven days of at least 40 mm on a VAS (0-100 mm, 0 = no pain, 100 = worst pain imaginable)
  • - Willingness to forego osteopathic treatment for the next 12 weeks if the study participant is randomized to the control group
  • - Ability to give informed consent
  • - Informed consent (in paper form) is available

排除标准

  • Important exclusion criteria:
  • - Pain in the most painful shoulder that requires urgent conventional medical treatment (e.g. muscle disease, recent trauma, SLAP (superior labrum anterior posterior) lesion)
  • - Peripheral and/or central neurological symptoms
  • - Diseases from the rheumatoid arthritis spectrum
  • - Shoulder surgery on the most painful shoulder within the last 6 months
  • - Generalized pain disorder such as fibromyalgia
  • - Treatment of cervical spine complaints with physical medicine currently or within the last 3 months before the start of the study
  • - Obesity with BMI =30 kg/m²
  • - Pregnancy or breastfeeding
  • - Presence of a serious acute and/or chronic organic or mental illness that does not allow participation in the therapy
  • - Lack of time resources to have the OM carried out
  • - Contraindications for non-steroidal anti-inflammatory drugs
  • - Taking centrally acting analgesics
  • - Treatment with OM within the last 6 months before the start of the study
  • - Expected lack of compliance with regard to study participation (e.g. notification that they do not wish to answer any further questions; limitation of general compliance ability in the case of dementia, severe alcohol abuse, drug abuse)
  • - Insufficient knowledge of the German language
  • - Participation in other studies
  • - No e-mail address available
  • - No skills or ability to operate or use tablets or computers independently
  • - Institute staff

研究者

发起方
Charité - Universitätsmedizin Berlin, Institut für Sozialmedizin, Epidemiologie und Gesundheitsökonomie

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