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祈祷与远程治疗研究的研究方法

Research methodology for studies of prayer and distant healing.

作者信息

Targ Elisabeth

机构信息

Complementary Medical Research Institute, California Pacific Medical Center, San Francisco 94115, USA.

出版信息

Complement Ther Nurs Midwifery. 2002 Feb;8(1):29-41. doi: 10.1054/ctnm.2001.0597.

Abstract

The double-blind randomized clinical trial is the gold standard for trials of prayer and distant healing. Adequate blinding and randomization procedures should be followed and documented. The intervention must be well defined (include frequency, amount of time and training and/or experience level of healers). Subjects should have risks and benefits of study participation explained to them and sign informed consent before enrollment. Populations should be homogeneous. Consider stratification for smaller samples. Baseline information, including psychological status, beliefs about prayer and healing and other sources of prayer and healing, should be collected from subjects in clinical trials. This should be examined as part of the final data analysis for contribution to outcomes. Objectively measurable outcomes with adequate variability should be chosen. Subject study participation activities such as clinical interviews, traveling to special sites. journaling or meditation should be minimized to avoid washing out a small effect. In clinical trials subjects should be asked if they believed they were in the treatment group and this information should be entered as a co-variate for data analysis. Healers/prayers should be treated in a collegial and respectful way. Their healing efforts (time. location, method) should be documented in a log and they should be periodically contacted and encouraged by experimenters if the study' is taking place over an extended period of time. Observational and outcomes research can add an important dimension to healing research. Qualitative studies may also make an important contribution and help guide development of future controlled trials.

摘要

双盲随机临床试验是祈祷与远程治疗试验的金标准。应遵循并记录充分的盲法和随机程序。干预措施必须明确界定(包括频率、时间量以及治疗师的培训和/或经验水平)。应向受试者解释参与研究的风险和益处,并在入组前签署知情同意书。研究人群应具有同质性。对于较小样本应考虑分层。在临床试验中,应从受试者收集基线信息,包括心理状态、对祈祷和治疗的信念以及其他祈祷和治疗来源。在最终数据分析中应检查这些信息对结果的贡献。应选择具有足够变异性的客观可测量结果。应尽量减少受试者参与研究的活动,如临床访谈、前往特殊地点、写日记或冥想,以避免消除微小效应。在临床试验中,应询问受试者是否认为自己在治疗组,并将此信息作为协变量输入进行数据分析。应对治疗师/祈祷者以 collegial 和尊重的方式对待。如果研究持续较长时间,他们的治疗努力(时间、地点、方法)应记录在日志中,并且实验人员应定期与他们联系并给予鼓励。观察性研究和结果研究可为治疗研究增添重要维度。定性研究也可能做出重要贡献,并有助于指导未来对照试验的开展。 (注:collegial 这个词在这里结合语境推测可能是“同行间友好合作的”之类意思,但直接翻译不太准确,保留英文供进一步确认其准确含义)

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