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Digital Medicine in Meditation (DigMed2)

2014年3月12日 更新者:Scripps Translational Science Institute
This study will investigate the acute response to meditation during a week-long meditation retreat at the Chopra Center as measured by the continuous, simultaneous monitoring of numerous biometric parameters in selected cohorts of experienced and novice meditators during periods of meditation and specific breathing techniques. Comparisons between cohorts as well as over time will allow for the identification of meditation and/or breathing-related changes.

研究概览

地位

完全的

详细说明

The biometric responses to meditation and breathing techniques will be compared between novice and experienced meditators, as well as initial versus final biometric responses in all participants stratified by cohort. Investigators hypothesize that novice meditators will experience a measurable change in response to mediation over the week-long retreat, whereas experienced meditators will demonstrate a more robust response than novice meditators on the first day of the retreat with less change over the retreat.

研究类型

观察性的

注册 (实际的)

40

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • California
      • Carlsbad、California、美国、92009
        • The Chopra Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Participants in this study will be a subset of 40 individuals from a total of ~200 who self-selected to participate in a week-long "Seduction of Spirit" retreat at The Chopra Center in the La Costa Resort in Carlsbad, CA. The 40 anticipated participants will be made up of 2 cohorts: experienced meditators and novice meditators.

描述

Inclusion Criteria:

  • Adult over age 18 who are already registered to participate in the week-long "Seduction of the Soul" retreat.
  • Capable of providing informed consent

Exclusion Criteria:

  • Chronic requirement for daily use of chronotropically active medications including beta-blockers, non-dihydropyridine calcium channel blockers, clonidine or beta-agonist inhalers.
  • Implantable pacemaker or cardioverter-defibrillator.
  • Known allergy to adhesives.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Experienced Meditators
Self-identified participants who confirm to having a regular meditation practice for at least 3 months and practiced at least 70 minutes per week.
Novice meditators
Self-identified participant who confirm to either having never seriously tried meditation, or who have not meditated more than once a week for at least 3 months

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Blood Pressure
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Non-invasive blood pressure
Participants will be measured at Day 1 and Day 5 of retreat
ECG
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
5-lead electrocardiogram
Participants will be measured at Day 1 and Day 5 of retreat
Respiration rate
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Respiration rate
Participants will be measured at Day 1 and Day 5 of retreat
Heart Rate
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Heart rate
Participants will be measured at Day 1 and Day 5 of retreat
Oxygen saturation (SpO2)
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Oxygen saturation
Participants will be measured at Day 1 and Day 5 of retreat
Skin temperature
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Skin temperature
Participants will be measured at Day 1 and Day 5 of retreat
Heart rate variability
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Variability in heart rate across a period of time.
Participants will be measured at Day 1 and Day 5 of retreat
EEG
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
14-lead Electroencephalogram
Participants will be measured at Day 1 and Day 5 of retreat
Stress level
大体时间:Participants will be measured at Day 1 and Day 5 of retreat
Stress level calculated from heart rate variability
Participants will be measured at Day 1 and Day 5 of retreat

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2013年10月1日

初级完成 (实际的)

2013年11月1日

研究完成 (实际的)

2013年11月1日

研究注册日期

首次提交

2013年10月17日

首先提交符合 QC 标准的

2013年10月28日

首次发布 (估计)

2013年11月3日

研究记录更新

最后更新发布 (估计)

2014年3月13日

上次提交的符合 QC 标准的更新

2014年3月12日

最后验证

2014年3月1日

更多信息

与本研究相关的术语

其他研究编号

  • 13 - 6251

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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