Improving Breast Health Knowledge Among Women Using a Gamified Metaverse-Based Platform

NCT ID: NCT06930898

Last Updated: 2025-04-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-12-01

Study Completion Date

2025-03-24

Brief Summary

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This randomized controlled trial aimed to evaluate the effectiveness of Mammoverse, a gamified metaverse-based educational platform, in improving breast health knowledge among women in China. Participants were randomly assigned to either a gamified or non-gamified version of the platform. Both groups received identical educational content, but only the gamified group experienced interactive game elements such as avatars, progress feedback, and rewards. Knowledge was assessed at baseline, immediately post-intervention, and at 4-week follow-up. The study found that the gamified platform significantly improved knowledge retention and participant engagement compared to the non-gamified version.

This ClinicalTrials.gov registration reflects only the randomized controlled trial (RCT) portion of a broader mixed-methods study that was approved by the University of Malaya Research Ethics Committee (Ref: UM.TNC2/UMREC\_3967). The full study protocol includes three methodological approaches, and this registration pertains specifically to the RCT component involving the Mammoverse platform. Other study components are not included in this registration.

Detailed Description

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Mammoverse is a 3D metaverse environment designed to promote breast health knowledge through immersive and interactive learning. The gamified version included user avatars, badges, tasks, and personalized feedback to increase motivation and engagement. The study recruited 72 women aged 18 and above, and used a pre-post-follow-up design. Outcome measures were based on an adapted 18-item Breast Health Literacy Questionnaire. The trial was conducted entirely online, with ethics approval from the University of Malaya Research Ethics Committee.

Conditions

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Health Education Breast Neoplasms

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants were randomly assigned in a 1:1 ratio to one of two parallel groups: a gamified version of the Mammoverse metaverse-based platform or a non-gamified version containing the same educational content.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Gamified Metaverse Education

Participants in this group used the Mammoverse platform with gamified features, including story-based missions, interactive tasks, point-based rewards, achievement badges, and virtual incentives. The educational content was delivered through immersive scenarios to enhance engagement and motivation in learning about breast health.

Group Type EXPERIMENTAL

Gamified Mammoverse Platform

Intervention Type BEHAVIORAL

A gamified, metaverse-based platform delivering breast health education through story-based tasks, interactive challenges, points, rewards, badges, and virtual incentives.

Non-Gamified Metaverse Education

Participants in this group accessed the Mammoverse platform without any gamified features. The virtual environment delivered identical breast health educational content, but without tasks, points, rewards, badges, or narrative elements.

Group Type ACTIVE_COMPARATOR

Standard Mammoverse Platform

Intervention Type BEHAVIORAL

A non-gamified version of the Mammoverse platform that provides the same breast health educational content.

Interventions

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Gamified Mammoverse Platform

A gamified, metaverse-based platform delivering breast health education through story-based tasks, interactive challenges, points, rewards, badges, and virtual incentives.

Intervention Type BEHAVIORAL

Standard Mammoverse Platform

A non-gamified version of the Mammoverse platform that provides the same breast health educational content.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Female participants aged 18 years and above
* Able to read and understand Chinese
* Access to a digital device and stable internet connection
* Willing to provide informed consent

Exclusion Criteria

* Cognitive impairment or mental health condition that affects participation
* Inability to complete the full intervention and follow-up sessions
* Incomplete baseline assessment
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Malaya

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Rui Li, PhD(c)

Role: PRINCIPAL_INVESTIGATOR

University of Malaya

Locations

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Online Recruitment - Hangzhou, Zhejiang, China

Hangzhou, Zhejiang, China

Site Status

University of Malaya

Kuala Lumpur, , Malaysia

Site Status

Countries

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China Malaysia

Other Identifiers

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UMREC_3967

Identifier Type: OTHER

Identifier Source: secondary_id

Mammo2025-RCT01

Identifier Type: -

Identifier Source: org_study_id

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