Effects of Internet-based Storytelling Programs in Reducing Mental Illness Stigma With Mediation by Interactivity and Stigma Content

Sponsor
Chinese University of Hong Kong (Other)
Overall Status
Completed
CT.gov ID
NCT05333848
Collaborator
(none)
263
1
4
2.2
119.5

Study Details

Study Description

Brief Summary

Mental illness stigma has been a concerning issue globally due to its adverse effects on the recovery of people with mental illness and may delay help-seeking for mental health out of the concern of being stigmatized. With technological advancement, Internet-based mental health stigma reduction interventions have been developed to combat mental illness stigma and the effects have been promising.

The present study aimed to examine the differential effects of Internet-based storytelling programs varied on level of interactivity and stigma content in reducing mental illness stigma.

In the present study, the investigator hypothesized that an Internet-based storytelling program with a combination of interactivity and stigma content would lead to the most significant reduction in public stigma, microaggression, and social distance from people with mental illnesses, followed by Internet-based storytelling program with stigma content-only and interactivity-only, compared with control. Secondly, the investigator hypothesized that the effects observed in stigma reduction would be mediated by perceived autonomy and immersiveness due to the presence of interactivity.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Internet-based storytelling programs with interactivity and stigma content
  • Behavioral: Internet-based storytelling programs with stigma content only
  • Behavioral: Internet-based storytelling programs with interactivity only
  • Behavioral: Internet-based storytelling programs with no interactivity and no stigma content
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
263 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
A 2x2 factorial design randomized controlled trialA 2x2 factorial design randomized controlled trial
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Effects of Internet-based Storytelling Programs in Reducing Mental Illness Stigma With Mediation by Interactivity and Stigma Content
Actual Study Start Date :
Dec 27, 2020
Actual Primary Completion Date :
Mar 4, 2021
Actual Study Completion Date :
Mar 4, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: COMBO condition

An interactive stigma content website.

Behavioral: Internet-based storytelling programs with interactivity and stigma content
Participants viewed an interactive stigma content website. Within 10 minutes post-experiment, participants completed the post-experiment questionnaire. One week after the experiment, participants completed the follow-up questionnaire.

Experimental: STIGMA condition

A non-interactive stigma content website.

Behavioral: Internet-based storytelling programs with stigma content only
Participants viewed a non-interactive stigma content website. Within 10 minutes post-experiment, participants completed the post-experiment questionnaire. One week after the experiment, participants completed the follow-up questionnaire.

Experimental: INTERACT condition

An interactive non-stigma content website.

Behavioral: Internet-based storytelling programs with interactivity only
Participants viewed an interactive non-stigma content website. Within 10 minutes post-experiment, participants completed the post-experiment questionnaire. One week after the experiment, participants completed the follow-up questionnaire.

Placebo Comparator: CONTROL condition

A non-interactive non-stigma content website.

Behavioral: Internet-based storytelling programs with no interactivity and no stigma content
Participants viewed a non-interactive non-stigma content website. Within 10 minutes post-experiment, participants completed the post-experiment questionnaire. One week after the experiment, participants completed the follow-up questionnaire.

Outcome Measures

Primary Outcome Measures

  1. Change from Baseline Public Stigma towards People with Mental Illness within 10 minutes post-experiment, and at 1-week follow-up [baseline, within 10 minutes post-experiment, and 1-week follow-up]

    The 21-item Public Stigma Scale-Mental Illness-Short Version was used to assess mental illness public stigma and personal advocacy. Each item was rated on a 6-point Likert scale from 1 (strongly disagree) to 6 (strongly agree). Reverse scoring was done for personal advocacy items. Higher scores indicated a higher level of public stigma towards people with mental illness.

  2. Change from Baseline Microaggression within 10 minutes post-experiment, and at 1-week follow-up [baseline, within 10 minutes post-experiment, and 1-week follow-up]

    Microaggression was measured by the 17-item Mental Illness Microaggressions Scale, which covers assumption of inferiority, patronization, and fear of mental illness. Each item was rated on a 4-point Likert scale from 1 (strongly disagree) to 4 (strongly agree). Higher scores indicated a higher level of mircroaggression.

  3. Change from Baseline Social Distance from People with Mental Illness within 10 minutes post-experiment, and at 1-week follow-up [baseline, within 10 minutes post-experiment, and 1-week follow-up]

    The 8-item Social Distancing Scale was used to measure the social distance from people with mental illnesses. Each item was rated on a 6-point Likert scale from 1 (very willing) to 6 (very unwilling). Higher scores indicated a higher level of social distance from people with mental illness.

  4. Perceived autonomy [within 10 minutes post-experiment]

    To assess perceived autonomy of the Web page experience, the 10-item Self Determination Scale (SDS) was used in the post-experiment questionnaire. Each item was a pair of opposite statements, where participants rated their level of perceived choice and self-awareness with a slider from 1 (only A feels true) to 5 (only B feels true). Higher scores indicated a higher level of perceived autonomy.

  5. Immersiveness [within 10 minutes post-experiment]

    The 15-item Transportation Scale was used to assess participants' immersiveness in the Web experience. It had a 4-point Likert scale from 1 (very much) to 4 (not at all). Items 2, 5 and 9 were framed negatively. All the items are scored in the direction that higher scores indicated a higher level of immersivenss.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • aged 18 years or above

  • able to read and understand Chinese

Exclusion Criteria:
  • less than 18 years of age

  • unable to read or understand Chinese

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Chinese University of Hong Kong Hong Kong Hong Kong HKG

Sponsors and Collaborators

  • Chinese University of Hong Kong

Investigators

  • Study Chair: Winnie Wing-Sze Mak, PhD, Chinese University of Hong Kong

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Hiu Ching Tiffany Fong, Principal Investigator, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT05333848
Other Study ID Numbers:
  • dre20024
First Posted:
Apr 19, 2022
Last Update Posted:
Apr 19, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hiu Ching Tiffany Fong, Principal Investigator, Chinese University of Hong Kong
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 19, 2022