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A VR Intervention for Promoting Prosocial Behavior and Well-being in Youth

T

The Hong Kong Polytechnic University

Status

Not yet enrolling

Conditions

Youth

Treatments

Behavioral: Prosocial VR intervention
Other: No intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT06454851
HSEARS20240214005-01

Details and patient eligibility

About

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.

Full 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).

Enrollment

160 estimated patients

Sex

All

Ages

15 to 19 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

160 participants in 2 patient groups

VR Intervention group
Experimental group
Description:
Participants in the intervention condition will be required to complete a 4-session gamified prosocial VR intervention program, one session a week for four consecutive weeks, each session lasts around 15-20 minutes.
Treatment:
Behavioral: Prosocial VR intervention
Waitlist control group
Sham Comparator group
Description:
Participants in the waitlist condition will be asked to continue their usual activity routines before their turn to receive the intervention.
Treatment:
Other: No intervention

Trial contacts and locations

0

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Central trial contact

Tao Zhang

Data sourced from clinicaltrials.gov

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