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临床试验/NCT03994809
NCT03994809已完成不适用

International Cross-sectional Study on the Effectiveness of Biofield Therapy for the Relief of Various Symptoms

MOA Health Science Foundation0 个研究点目标入组 12,000 人开始时间: 2008年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12,000
主要终点
adjusted odds ratio of the factors associated with the changes in symptoms

研究概览

简要总结

Participants from 14 different countries received a single session of biofield therapy (Okada Purifying Therapy) lasting 30 minutes or longer from the volunteer practitioners. Before and after the therapy, they reported the severity of physical pain, anxiety/depression, dizziness/palpitation, and overall symptoms. The team compared the effectiveness/safety of biofield therapy between countries and analyzed the factors associated with the outcomes.

详细描述

Participants aged 16 or older from 14 different countries (Japan, USA, Argentina, Brazil, Chile, Mexico, Peru, Taiwan, Thai, South Korea, Belgium, France, Portugal, and Spain) received a single session of biofield therapy (Okada Purifying Therapy) lasting 30 minutes or longer from the volunteer practitioners in their country of residence. Before and after the intervention, they reported each severity level of physical pain, anxiety/depression, dizziness/palpitation, and overall symptoms. The team compared the improvement/exacerbation rate of a single session of biofield therapy between the countries, and examined the adjusted odds ratio of the variables associated with the changes in each category of symptoms in a real-world setting.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Individuals who agreed to receive a single session of biofield therapy for 30 minutes or longer from the volunteer investigators.
  • Individuals who were able to self-evaluate the change of their symptoms.
  • Individuals who were competent to answer the questionnaires.
  • Individuals who were aged 16 or older.

排除标准

  • no specific exclusion criteria

结局指标

主要结局

adjusted odds ratio of the factors associated with the changes in symptoms

时间窗: Up to one year after all the data were collected.

Logistic regression analyses

improvement/exacerbation rate of symptoms after a single session of biofield therapy

时间窗: Up to one year after all the data were collected.

The Mann-Whitney test was conducted to compare the improvement/exacerbation rates between countries.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kiyoshi Suzuki

President

MOA Health Science Foundation

相似试验

International Study of Biofield Therapy | 临床试验