A VR Intervention for Prosocial Behavior and Well-being Among Adolescents
Effectiveness of a Virtual Reality (VR) Intervention for Prosocial Behavior and Well-being Among Adolescents: A Randomized Controlled Trial
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Tao Zhang
- Phone Number: 852-94233827
- Email: tao-t.zhang@connect.polyu.hk
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- School students aged 10-16 (i.e., primary 5 to secondary 5);
- Able to communicate in Chinese.
Exclusion Criteria:
- Significant cognitive impairment;
- Self-reported severe motion sickness;
- Uncorrected visual impairment.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
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Experimental: Prosocial VR Intervention
Participants in the VR intervention group will engage in a five-week gamified prosocial VR intervention program.
The intervention will consist of five weekly sessions, each lasting between 10 to 15 minutes.
Each session will depict a different daily life scenario, including a home, school, street, park, and shopping mall.
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A five-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 five weekly sessions, each lasting between 10 to 15 minutes.
Each session will depict a different daily life scenario-home, school, street, park, and shopping mall, 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.
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No Intervention: Waitlist control group
Participants in the waitlist condition will not receive VR intervention during the study.
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What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Prosocial attitudes
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Three items assessing prosocial attitudes will be revised from the Prosocial Orientation Questionnaire.
Participants will rate each item on a 6-point Likert scale, ranging from 1 (strongly disagree) to 6 (strongly agree).
Higher scores on the scale indicate a greater presence of positive prosocial attitudes.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Prosocial identity
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Internalization subscale of the Self Importance of Moral Identity Scale (SIMIS) will be used to measure the construct of prosocial identity.
Participants will rate each item on a 7-point Likert scale, ranging from 1 (strongly disagree) to 7 (strongly agree).
Elevated scores on the scale indicate a greater degree of prosocial identity.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Prosocial intention
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Prosocial Behavioral Intentions Scale (PBIS) will be employed to evaluate individuals' future intentions to engage in prosocial behavior.
Participants will rate each item on a 7-point Likert scale, ranging from 1 (Definitely would not do this) to 7 (Definitely would do this).
Increased scores on the scale indicate a greater inclination towards prosocial intentions.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Attitudes toward helping others
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Attitudes toward Helping Others Scale (AHO) will be employed to assess individuals' attitudes towards helping others.
Each item will be rated on a 5-point Likert scale, ranging from 1 (strongly disagree) to 5 (strongly agree).
Elevated scores on the scale indicate a greater presence of positive attitudes towards helping others.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Altruism
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Two items from the Preference Survey Module (PSM) will be modified to measure altruism.
One example item is as follows: "Imagine the following scenario: you have won 1,000 Euros in a lottery.
Considering your present circumstances, how much of the prize would you donate to a charitable cause?
(Values between 0 and 1000 are permissible)."
Higher scores on this item indicate a higher level of altruistic behavior or tendencies.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Empathy
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Single Item Trait Empathy Scale (SITES) will be utilized to assess levels of empathy.
Participants will rate this item on a 7-point Likert scale, ranging from 1 (strongly disagree) to 7 (strongly agree), with higher scores indicating a greater degree of empathy.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Life satisfaction
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Satisfaction with Life Scale (SWLS) will be employed to evaluate levels of life satisfaction.
Participants will rate each item on a 7-point Likert scale, ranging from "Strongly Disagree" to "Strongly Agree."
Elevated scores on the scale indicate greater levels of life satisfaction.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Subjective happiness
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Subjective Happiness Scale (SHS) will be utilized to assess participants' subjective happiness.
Each item will be rated on a 7-point Likert scale.
Elevated scores on the scale indicate a greater level of subjective happiness.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Affect
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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The Emmons Mood Indicator will be employed to measure affect, encompassing 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).
Elevated scores on the scale indicate a higher level of affect.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Gratitude
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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One item from the Gratitude Adjective Checklist (GAC) will be used to measure participants' gratitude.
This item will be rated on a 7-point Likert scale.
A higher score indicate a higher level of gratitude.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Subjective vitality
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Three items from the Subjective Vitality Scale (SVS) will be used to measure participants' subjective vitality.
Each item will be rated on a 7-point Likert scale.
Higher scores indicate a higher level of subjective vitality.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Self-esteem
Time Frame: Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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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.
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Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)
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Daily well-being
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily well-being will be assessed using a single item ("How do you feel right now?") adapted from the Well-Being Manifestations Measure Scale (WBMMS) using a sliding scale ranging from 0 (not good at all) to 100 (very good).
A higher score indicates a higher level of daily well-being.
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Daily monitoring for 5 weeks during the intervention
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Daily prosocial act
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily prosocial act will be measured by one item: "How many acts have you engaged today that involve helping someone else or doing something for a good cause?"
Participants will indicate the number of prosocial acts from a drop-down menu ranging from 0 to 10+.
The response of "0" will be classified as "no prosocial engagement," and responses of "1" or more will be classified as "having engaged in prosocial acts."
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Daily monitoring for 5 weeks during the intervention
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Daily subjective happiness
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily subjective happiness will be measured using a condensed 2-item adaptation of the Subjective Happiness Scale (SHS).
The first item will assess their self-perceived general happiness today on a scale from 1 (not at all happy) to 7 (very happy).
The second item will gauge their comparative happiness to their peers during the same timeframe, ranging from 1 (less happy) to 7 (more happy).
Higher scores indicate a higher level of daily subjective happiness.
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Daily monitoring for 5 weeks during the intervention
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Daily subjective vitality
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily subjective vitality will be assessed using 3 representative items from the 7-item Subjective Vitality Scale (SVS).
All items will be rated on a 7-point scale (1 = not at all true to 7 = very true).
Higher scores indicate a higher level of daily subjective vitality.
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Daily monitoring for 5 weeks during the intervention
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Daily affect
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily affect will be evaluated using the 9-item Emmons Mood Indicator.
Participants will be instructed to rate the extent to which they experienced each emotion today using a 7-point scale (ranging from 1 = not at all to 7 = extremely).
Elevated scores on the scale indicate a higher level of daily affect.
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Daily monitoring for 5 weeks during the intervention
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Daily gratitude
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily gratitude will be measured using one item from the Gratitude Adjective Checklist (GAC).
This item will be rated on a 7-point Likert scale.
A higher score indicates a higher level of daily gratitude.
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Daily monitoring for 5 weeks during the intervention
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Daily psychological needs
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily psychological needs will be assessed using a 9-item Basic Psychological Needs Scale (BPNS).
Each subscale, namely competence, autonomy, and relatedness, consists of 3 items rated on a 7-point scale (ranging from 1 = not at all true to 7 = very true).
Higher scores indicate a higher level of daily psychological needs.
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Daily monitoring for 5 weeks during the intervention
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Daily self-esteem
Time Frame: Daily monitoring for 5 weeks during the intervention
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Daily self-esteem will be evaluated using 2 items from the Rosenberg Self-Esteem Scale (Rosenberg, 1965).
Ratings will be evaluated on a 4-point scale (1 = strongly disagree to 4 = strongly agree).
Higher scores indicate a higher level of daily self-esteem.
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Daily monitoring for 5 weeks during the intervention
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Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Feelings in the VR
Time Frame: immediately after the intervention (post-intervention)
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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".
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immediately after the intervention (post-intervention)
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Levels of difficulty
Time Frame: immediately after the intervention (post-intervention)
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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".
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immediately after the intervention (post-intervention)
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Levels of interest
Time Frame: immediately after the intervention (post-intervention)
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Two items will be used to measure the levels of difficulty.
Items are "This game is very interesting" and "I like this game".
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immediately after the intervention (post-intervention)
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Intervention satisfaction
Time Frame: immediately after the intervention (post-intervention)
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Intervention satisfaction will be assessed using the Client Satisfaction Questionnaire-8 (CSQ-8).
Participants will rate each item on a 4-point Likert scale, with "1" indicating the lowest degree of satisfaction and "4" representing the highest.
Elevated scores on the scale reflect greater levels of intervention satisfaction.
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immediately after the intervention (post-intervention)
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Other Outcome Measures
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Socio-demographic variables
Time Frame: Baseline (pre-intervention)
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The study will collect socio-demographic variables including gender, age, level of education, and family income.
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Baseline (pre-intervention)
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Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Bryant HUI, Ph.D., The Hong Kong Polytechnic University
Study record dates
Study Major Dates
Study Start (Estimated)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- HSEARS20221208004-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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