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临床试验/NCT01852500
NCT01852500已完成4 期

Are Newborns Conscious of the Placebo Effect? Result From an RCT in Osteopathy

European Institute for Evidence Based Osteopathic Medicine2 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2010年11月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
250
试验地点
2
主要终点
Evaluate the effectiveness of sham OMT in reducing LOS

研究概览

简要总结

Results from previous studies suggest the association between Osteopathic Manipulative Treatment (OMT) and length of stay (LOS) reduction in a population of preterm infants.

The primary objective of the present study is to evaluate the effectiveness of sham OMT in reducing LOS in a sample of preterm newborns, in order to investigate whether previous clinical results could be related to a hypothetical placebo effect.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
29 Weeks 至 37 Weeks(Child)
性别
All
接受健康志愿者

入选标准

  • preterm infants born at age between 29 and 37 weeks
  • sham osteopathic treatment performed < 14 days after birth
  • preterm infants born in the same hospital

排除标准

  • gestational age < 29, > 37 weeks;
  • sham osteopathic treatment performed > 14 days after birth;
  • newborn transferred to/from other hospital;
  • newborn from to HIV seropositive and/or drug addict mother;
  • newborn with genetic disorders, congenital abnormalities, cardiovascular abnormalities, neurological disorders, proven or suspected necrotizing enterocolitis with or without gastrointestinal perforation, proven or suspected abdominal obstruction, pre- and/or post-surgery patients, pneumoperitoneum and/or atelectasis.

结局指标

主要结局

Evaluate the effectiveness of sham OMT in reducing LOS

时间窗: participants will be followed for the duration of hospital stay, an expected average of 4 weeks

次要结局

  • pre-post difference in weight gain(participants will be followed for the duration of hospital stay, an expected average of 4 weeks)

研究者

发起方
European Institute for Evidence Based Osteopathic Medicine
申办方类型
Other
责任方
Sponsor

研究点 (2)

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