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Healing Stigma Through Stories

2026年7月10日 更新者:Li-Ting Huang、National Yang Ming Chiao Tung University

Healing Stigma Through Stories: Learning From International Practices to Develop and Evaluate a Narrative Program for Individuals With Schizophrenia

This study is the first phase of the research project. The purpose of this phase is to develop and refine a narrative-based intervention designed to reduce self-stigma among people with schizophrenia.

A small pilot study will be conducted with 24 participants recruited from halfway houses in northern Taiwan. Eligible participants will receive the intervention, which consists of four group sessions and four individual sessions, held once a week for a total of eight weeks. The program uses narrative therapy techniques to help participants explore their personal experiences and reduce self-stigma. Participants will complete a workbook during the program, and the written content will be analyzed to better understand their experiences with stigma. Any personal information will be removed to protect participants' privacy. Before and after the intervention, participants will complete questionnaires on self-stigma, depression, social functioning, well-being, hope, and recovery. Information on medication use will also be collected. Group and individual sessions will be audio-recorded for research purposes. The questionnaire data and recordings will be used to evaluate the feasibility and preliminary effects of the intervention.

研究概览

研究类型

介入性

注册 (估计的)

24

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。

学习联系方式

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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Aged 18 years or older.
  • Diagnosed with schizophrenia or schizoaffective disorder.
  • Clinically stable at the time of study enrollment.
  • Able to communicate in Mandarin Chinese or Taiwanese.
  • Able to read and write and complete study questionnaires.

Exclusion Criteria:

  • Individuals who lack the capacity to provide informed consent. Decision-making capacity will be assessed using a 10-item true/false questionnaire adapted from Okoli et al. (2018). Participants who answer fewer than 7 questions correctly will be excluded. Those who answer 7 or more questions correctly will receive an additional explanation from the research team. Only individuals who demonstrate a complete understanding of the study after this explanation will be enrolled.
  • Unwilling to have the intervention sessions audio-recorded.

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:其他
  • 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:Healing Stigma through Stories
Four group sessions and four individual sessions, held once a week for a total of eight weeks. The program uses narrative therapy techniques to help participants explore their personal experiences and reduce self-stigma.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
The Internalized Stigma of Mental Illness Scale
大体时间:At baseline(T0) and through study completion, an average of 8 weeks
At baseline(T0) and through study completion, an average of 8 weeks

次要结果测量

结果测量
大体时间
Beck Depression Inventory-II
大体时间:At baseline(T0) and through study completion, an average of 8 weeks
At baseline(T0) and through study completion, an average of 8 weeks
Self-Reported Graphic version of the Personal and Social Performance Scale
大体时间:At baseline(T0) and through study completion, an average of 8 weeks
At baseline(T0) and through study completion, an average of 8 weeks
Subjective Happiness Scale
大体时间:At baseline(T0) and through study completion, an average of 8 weeks
At baseline(T0) and through study completion, an average of 8 weeks
Herth Hope Index
大体时间:At baseline(T0) and through study completion, an average of 8 weeks
At baseline(T0) and through study completion, an average of 8 weeks
The questionnaire about the process of recovery
大体时间:At baseline(T0) and through study completion, an average of 8 weeks
At baseline(T0) and through study completion, an average of 8 weeks

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 (估计的)

2026年8月1日

初级完成 (估计的)

2027年7月1日

研究完成 (估计的)

2027年7月1日

研究注册日期

首次提交

2026年7月7日

首先提交符合 QC 标准的

2026年7月10日

首次发布 (实际的)

2026年7月16日

研究记录更新

最后更新发布 (实际的)

2026年7月16日

上次提交的符合 QC 标准的更新

2026年7月10日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

其他研究编号

  • NYCU115040AF
  • 115-2314-B-A49 -082 - (其他赠款/资助编号:National Science and Technology Council)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

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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