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

Last updated: May 23, 2024
Sponsor: Chinese University of Hong Kong
Overall Status: Completed

Phase

N/A

Condition

Mood Disorders

Treatment

Online psychoeducational program

Clinical Study ID

NCT05519748
6906334
  • Ages 18-64
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 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 orabove) at a baseline screening

  • able to understand and communicate in Chinese-Cantonese

  • have access to the internet.

Exclusion

Exclusion Criteria:

  • Individuals who have a reading disorder, cognitive impairment, dementia, orintellectual disabilities

  • Individuals who are participating in any research studies

  • Individuals who had participated in our previous feasibility study of the sameintervention

Study Design

Total Participants: 101
Treatment Group(s): 1
Primary Treatment: Online psychoeducational program
Phase:
Study Start date:
September 01, 2022
Estimated Completion Date:
November 30, 2023

Connect with a study center

  • The Chinese University of Hong Kong

    Hong Kong,
    Hong Kong

    Site Not Available

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