Skip to main content
Clinical Trials/NCT05519748
NCT05519748CompletedNot Applicable

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 site in 1 country101 target enrollmentStarted: September 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
101
Locations
1
Primary Endpoint
Brief Coping Orientation to Problems Experienced Inventory (Brief-COPE)

Study Overview

Brief 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 64 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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 or above) at a baseline screening
  • •able to understand and communicate in Chinese-Cantonese
  • •have access to the internet.

Exclusion Criteria

  • •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

Arms & Interventions

Online psychoeducational program

Experimental

The intervention group will receive an online psychoeducational program for 8 weeks. The psychoeducation package consists of 16 different sets of reading materials and post-session writing/reflection exercises, which will be delivered to the participants twice a week. The program is designed to be a brief, trauma-informed, dissociation-focused education package that aims to enable users to better understand and cope with their post-traumatic and dissociative reactions and related life challenges. There are specific psychoeducation elements in each session, such as: (1) safety issues planning, (2) understanding the impacts of trauma and stress, (3) understanding the concept of dissociation and integration of the personality, (4) identifying and coping with the post-traumatic and dissociative symptoms, (5) identifying trauma-related cognitive distortions.

Intervention: Online psychoeducational program (Behavioral)

Waitlist control

Other

The waitlist control group will receive an online psychoeducational program for 8 weeks a week after the completion of the two-month follow-up in the intervention group. The psychoeducation package is identical to the program in the intervention group.

Intervention: Online psychoeducational program (Behavioral)

Outcomes

Primary Outcomes

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

Time Frame: 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.

Secondary Outcomes

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

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lam Kam Ki Stanley

Research Assistant Professor

Chinese University of Hong Kong

Study Sites (1)

Loading locations...

Similar Trials