NCT06504069

Brief Summary

The aim of this project is to examine the effectiveness of a gamified prosocial VR intervention.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P75+ for not_applicable

Timeline
4mo left

Started Sep 2024

Typical duration for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress84%
Sep 2024Sep 2026

First Submitted

Initial submission to the registry

June 26, 2024

Completed
20 days until next milestone

First Posted

Study publicly available on registry

July 16, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

September 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2025

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Expected
Last Updated

July 16, 2024

Status Verified

April 1, 2024

Enrollment Period

1 year

First QC Date

June 26, 2024

Last Update Submit

July 10, 2024

Conditions

Outcome Measures

Primary Outcomes (20)

  • Prosocial attitudes

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Prosocial identity

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Prosocial intention

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Attitudes toward helping others

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Altruism

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Empathy

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Life satisfaction

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Subjective happiness

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Affect

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Gratitude

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • Subjective vitality

    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.

    Baseline (pre-intervention); immediately after the intervention (post-intervention); 1 month after intervention (follow-up)

  • 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)

  • Daily well-being

    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.

    Daily monitoring for 5 weeks during the intervention

  • Daily prosocial act

    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."

    Daily monitoring for 5 weeks during the intervention

  • Daily subjective happiness

    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.

    Daily monitoring for 5 weeks during the intervention

  • Daily subjective vitality

    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.

    Daily monitoring for 5 weeks during the intervention

  • Daily affect

    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.

    Daily monitoring for 5 weeks during the intervention

  • Daily gratitude

    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.

    Daily monitoring for 5 weeks during the intervention

  • Daily psychological needs

    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.

    Daily monitoring for 5 weeks during the intervention

  • Daily self-esteem

    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.

    Daily monitoring for 5 weeks during the intervention

Secondary Outcomes (4)

  • Intervention satisfaction

    immediately after the intervention (post-intervention)

  • Feelings in the VR

    immediately after the intervention (post-intervention)

  • Levels of difficulty

    immediately after the intervention (post-intervention)

  • Levels of interest

    immediately after the intervention (post-intervention)

Other Outcomes (1)

  • Socio-demographic variables

    Baseline (pre-intervention)

Study Arms (2)

Prosocial VR Intervention

EXPERIMENTAL

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.

Behavioral: Prosocial VR intervention

Waitlist control group

NO INTERVENTION

Participants in the waitlist condition will not receive VR intervention during the study.

Interventions

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.

Prosocial VR Intervention

Eligibility Criteria

Age10 Years - 16 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17)

You may qualify if:

  • School students aged 10-16 (i.e., primary 5 to secondary 5);
  • Able to communicate in Chinese.

You may not qualify if:

  • Significant cognitive impairment;
  • Self-reported severe motion sickness;
  • Uncorrected visual impairment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Officials

  • Bryant HUI, Ph.D.

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 26, 2024

First Posted

July 16, 2024

Study Start

September 1, 2024

Primary Completion

September 1, 2025

Study Completion (Estimated)

September 1, 2026

Last Updated

July 16, 2024

Record last verified: 2024-04