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Expressive Writing for COVID-19 Resilience

2020年10月14日 更新者:Duke University
The purpose of this study is to determine the impact of a 6-week, virtually-delivered expressive writing intervention on resilience in a cohort of individuals currently navigating the COVID-19 pandemic during spring 2020.

研究概览

地位

完全的

详细说明

The purpose of this study is to determine the impact of a 6-week, virtually-delivered expressive writing intervention on resilience in a cohort of individuals currently navigating the COVID-19 pandemic during spring 2020.

Eligible subjects will be adults who are able to read and write in English and are cognitively able to provide informed consent. Potential subjects will be recruited through the Duke Health & Well-Being email lists. The entirely virtual 6-week expressive writing intervention will be delivered via Zoom, REDCap, and email, and subjects will complete measures at baseline, 6 weeks, and 10 weeks (1 month post-intervention). Each week of the intervention will invite participants to complete a series of expressive writing assignments designed to support emotional expression and cultivate resilience, and the assignments will take approximately 60-90 minutes each week to complete.

The primary outcome is the 25-item Connor-Davidson Resilience Scale (CD-RISC). Other measures will include a basic demographics survey, questions about COVID-19 impact, post-writing surveys collected after the writing assignments, the 10-item Perceived Stress Scale (PSS), the Center for Epidemiologic Studies Depression Scale-Revised, and the 21-item Post -Traumatic Growth Inventory (PTGI). Participants will also have the option to share the content of their writing assignments with the research team if they choose.

The risks of participation in this study are minimal and include the risk of mild sadness after the writing assignments and the risk of loss of confidentiality.

研究类型

介入性

注册 (实际的)

63

阶段

  • 不适用

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

    • North Carolina
      • Durham、North Carolina、美国、27705
        • Duke Integrative Medicine

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

有资格学习的性别

全部

描述

Inclusion Criteria:

Potential subjects will be considered eligible if they feel they have been personally impacted by circumstances surrounding COVID-19. Other eligibility criteria include:

  • Able to speak, read, write, and understand English
  • Cognitively able to provide consent
  • Ability to participate in a 6-week intervention delivered via Zoom, REDCap, and email

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

  • 主要用途:支持治疗
  • 分配:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Expressive writing

The expressive writing intervention consists of a 6-week, virtually-delivered writing program. Each week, participants meet for 90 minutes via Zoom and will be guided through writing prompts designed to encourage emotional expression and enhance personal resilience. The progression of writing exercises flows as follows:

  • Week 1: Writing to expressive difficult emotions
  • Week 2: Writing to release & integrate difficult emotions
  • Week 3: Writing to nurture gratitude
  • Week 4: Writing to enhance strengths & resources
  • Week 5: Writing to cultivate positive meaning & savor goodness
  • Week 6: Writing to invite insight, perspective, & growth

The expressive writing intervention consists of a 6-week, virtually-delivered writing program. Each week, participants meet for 90 minutes via Zoom and will be guided through writing prompts designed to encourage emotional expression and enhance personal resilience. The progression of writing exercises flows as follows:

  • Week 1: Writing to expressive difficult emotions
  • Week 2: Writing to release & integrate difficult emotions
  • Week 3: Writing to nurture gratitude
  • Week 4: Writing to enhance strengths & resources
  • Week 5: Writing to cultivate positive meaning & savor goodness
  • Week 6: Writing to invite insight, perspective, & growth

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
弹力
大体时间:3个月
Connor-Davidson 复原力量表 (CD-RISC)
3个月

次要结果测量

结果测量
措施说明
大体时间
Perceived stress
大体时间:3 months
Perceived Stress Scale-10 (PSS10)
3 months
Depression symptoms
大体时间:3 months
Center for Epidemiologic Studies Scale - Revised (CESDR)
3 months
Post-traumatic growth
大体时间:3 months
Post Traumatic Growth Inventory (PTGI)
3 months

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。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

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 (实际的)

2020年5月26日

初级完成 (实际的)

2020年8月17日

研究完成 (实际的)

2020年8月17日

研究注册日期

首次提交

2020年10月12日

首先提交符合 QC 标准的

2020年10月14日

首次发布 (实际的)

2020年10月19日

研究记录更新

最后更新发布 (实际的)

2020年10月19日

上次提交的符合 QC 标准的更新

2020年10月14日

最后验证

2020年10月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

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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