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临床试验/NCT05519748
NCT05519748已完成不适用

Effectiveness of an Online Psychoeducation Program for Improving Coping in People With a High Level of Dissociative Symptoms: A Pilot Randomized Waitlist-controlled Trial

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 101 人开始时间: 2022年9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
101
试验地点
1
主要终点
Brief Coping Orientation to Problems Experienced Inventory (Brief-COPE)

研究概览

简要总结

Subject Population Our study's target population is people with pathological dissociation in the community.

Research Design A pilot randomized waitlist-controlled trial will investigate the effects of an online psychoeducation program on coping, symptom management, and self-efficacy of people with pathological dissociation immediately (posttest-1) and 2-month (posttest-2) post-intervention. Supplementary semi-structured interviews will be conducted for process evaluation. The analysis and reporting of the trial will strictly follow the CONSORT guidelines.

Instrument The primary outcome of our study is the coping ability of individuals with pathological dissociation, which will be assessed by the Brief Coping Orientation to Problems Experienced Inventory (Brief-COPE). The secondary outcome measures are dissociative symptoms, emotional regulation, and self-efficacy, which would be assessed by the Dissociative Experiences Scale-Taxon (DES-T), the Emotion Regulation Questionnaire (ERQ), and the General Self-Efficacy Scale (GSES) accordingly.

Procedure The online psychoeducation program is developed based on an integrative theoretical framework that integrates the Stress and Coping model, Cognitive-Behavioural Theory, Bandura's self-efficacy theory, and findings of our previous feasibility studies on this psychoeducational program. Participants will be recruited via posting on social media and online forums. A 16-session online psychoeducation program will be delivered to the participants in eight weeks.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • agree to give informed consent and participate
  • aged 18 or above
  • self-reported symptoms or experiences of pathological dissociation
  • screened positive on the Chinese version of the DES-T (i.e., DES-T score 20 or above) at a baseline screening
  • able to understand and communicate in Chinese-Cantonese
  • have access to the internet.

排除标准

  • Individuals who have a reading disorder, cognitive impairment, dementia, or intellectual disabilities
  • Individuals who are participating in any research studies
  • Individuals who had participated in our previous feasibility study of the same intervention

结局指标

主要结局

Brief Coping Orientation to Problems Experienced Inventory (Brief-COPE)

时间窗: Immediately and two months after completion of the intervention in the experimental group

Change in participants' coping strategies, as assessed using the Brief-COPE. This measure has 28 items and is a commonly used self-report measure of coping strategies. The Chinese version of the Brief-COPE had excellent internal consistency, test-retest reliability and content validity. Higher scores indicate more significant use of that specific coping strategy.

次要结局

  • Dissociative Experiences Scale-Taxon (DES-T)(Immediately and two months after completion of the intervention in the experimental group)

研究者

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

Lam Kam Ki Stanley

Research Assistant Professor

Chinese University of Hong Kong

研究点 (1)

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