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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06454851
Other study ID # HSEARS20240214005-01
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 1, 2024
Est. completion date May 31, 2025

Study information

Verified date May 2024
Source The Hong Kong Polytechnic University
Contact Tao Zhang
Phone 852-9423-3827
Email tao-t.zhang@connect.polyu.hk
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of the present project is to develop a gamified prosocial VR intervention for youth transitioning from secondary to tertiary education, and to test the effectiveness of the gamified prosocial VR intervention for promoting prosocial behavior and well-being.


Description:

Targeting youth transitioning from secondary to tertiary education, the proposed project will adopt evidence-based intervention programs that use digital technologies to promote prosocial behavior and well-being, thereby supporting better intrapersonal and interpersonal development. The investigators aim to develop a gamified prosocial VR intervention for youth transitioning from secondary to tertiary education and to test its effectiveness through a randomized controlled trial (RCT).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 160
Est. completion date May 31, 2025
Est. primary completion date May 1, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 19 Years
Eligibility Inclusion Criteria: - Age 15-19 - Secondary 6 to college year 1 - Can read traditional Chinese and understand Cantonese Exclusion Criteria: - History of photosensitive epilepsy - Impairment of stereoscopic vision - Balance problems

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Prosocial VR intervention
A four-week gamified prosocial VR intervention program based on literature review and relevance to the local contexts will be developed for the proposed project. The intervention will be expanded to include four weekly sessions, each lasting between 15 to 20 minutes. Each session will depict a different daily life scenario-campus, lecture hall, canteen, and library, respectively. During each session, participants will engage in a series of tasks that incorporate elements of prosocial behavior or helping actions within the scene. These tasks are designed to be more comprehensive and interactive, ensuring that participants are fully immersed in the experience for the entire duration of the session.
Other:
No intervention
The waitlist control group will not receive the intervention during the study.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
The Hong Kong Polytechnic University

Outcome

Type Measure Description Time frame Safety issue
Other Socio-demographic variables The following socio-demographic variables such as gender, age, level of education, and family income will be collected. Baseline (pre-intervention)
Primary Prosocial behavior The Prosocialness Scale for Adults (PSA) will be used to measure prosocial behavior. Each item will be rated on a 5-point Likert scale, ranging from 1 (never/almost never true) to 5 (almost always/always true). Higher scores indicate a higher level of prosocial behavior. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Prosocial attitudes Three items of prosocial attitudes will be revised from the Prosocial Orientation Questionnaire. Each item will be rated on a 6-point Likert scale, ranging from 1 (strongly disagree) to 6 (strongly agree). Higher scores indicate more positive prosocial attitudes. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Prosocial identity The Internalization subscale of the Self Importance of Moral Identity Scale (SIMIS) will be adapted to assess the prosocial identity. Each item will be rated on a 7-point Likert scale, ranging from 1 (strongly disagree) to 7 (strongly agree). Higher scores indicate a higher level of Prosocial identity. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Prosocial intention The Prosocial Behavioral Intentions Scale (PBIS) will be used to assess people's intentions to behave prosocially in the future. Each item will be rated on a 7-point Likert scale, ranging 1 (Definitely would not do this) to 7 (Definitely would do this). Higher scores indicate a higher level of prosocial intention. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Attitudes toward helping others The Attitudes toward helping others scale (AHO) will be used to test attitudes towards helping others. Each item will be rated on a 5-point Likert scale, ranging from 1 (strongly disagree) to 5 (strongly agree). Higher scores indicate more positive attitudes toward helping others. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Altruism Two items from Preference Survey Module (PSM) will be adapted to assess altruism. For example, one item is: "Imagine the following situation: you won 1,000 Euro in a lottery. Considering your current situation, how much would you donate to charity? (Values between 0 and 1000 are allowed)". Elevated scores on this item reflect a greater degree of altruistic. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Online prosocial behavior The Online Prosocial Behavior Scale (OPBS) will be used to measure online prosocial behavior. Each item will be rated on a 7-point Likert scale, ranging 1 (never) to 7 (always). Higher scores indicate a higher level of online prosocial behavior. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Empathy The Single Item Trait Empathy Scale (SITES) will be used to measure empathy. This item will be rated on a 7-point Likert scale, ranging from 1 (strongly disagree) to 7 (strongly agree), with a higher score indicates a higher level of empathy. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Subjective happiness The Subjective Happiness Scale (SHS) will be used to measure participants' subjective happiness. Each item will be rated on a 7-point Likert scale. Higher scores indicate a higher level of subjective happiness. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Life satisfaction The Satisfaction with Life Scale (SWLS) will be used to measure life satisfaction. Each item will be rated on a 7-point Likert scale ranging from "Strongly Disagree" to "Strongly Agree. Higher scores indicate higher levels of life satisfaction. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Flourishing The Flourishing Scale (FS) will be used to measure flourishing. Each statement is answered using a 7-point Likert scale (7 - strongly agree to 1 - strongly). Higher scores indicate a higher level of flourishing. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Self-esteem The Rosenberg Self-esteem Scale (RSE) will be used to measure self-esteem. Each item will be rated on a 4-point Likert scale, ranging from 1 (strongly agree) to 4(strongly disagree). Higher scores indicate higher levels of self-esteem. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Affect The Emmons Mood Indicator will used to measure affect. it measures two dimensions: Positive Affect and Negative Affect. Each item will be rated on a 7-point Likert scale, ranging from 1 (not at all) to 7 (extremely). Higher scores indicate a higher level of affect. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Mental health The Patient Health Questionnaire-4 (PHQ-4) will be used to measure mental health. Each item will be rated on a 4-point Likert scale: "0" for "not at all," "1" for "several days," "2" for "more than half the days," and "3" for "nearly every day." Higher scores suggest a higher likelihood of experiencing significant depression and anxiety symptoms. Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
Primary Diary measures State prosocial behavior outcomes and well-being outcomes will be measured. Daily monitoring for four weeks during the intervention
Secondary Feelings in the VR Two items will be uesd to measure the sense of reality. Items are "I feel that the maze seemed very much like the one in the real world" and "The game scene made me feel like I was truly there". immediately after the intervention (post-intervention)
Secondary Levels of difficulty Two items will be used to measure the levels of difficulty. Items are "The game is very difficult" and "The game is too difficult to operate". immediately after the intervention (post-intervention)
Secondary Levels of interest Two items will be used to measure the levels of difficulty. Items are "This game is very interesting" and "I like this game". immediately after the intervention (post-intervention)
Secondary Intervention satisfaction The Client Satisfaction Questionnaire-8 (CSQ-8) will used to test Intervention satisfaction. Each item will be rated on a 4-point Likert scale where "1" indicates the lowest degree of satisfaction and "4," the highest. Higher scores indicate higher intervention satisfaction. immediately after the intervention (post-intervention and only in the last week)
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