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Effectiveness of Metaverse Space-based Exercise Video Distribution in Young Adults

Effectiveness of Metaverse Space-based Exercise Video Distribution in Young Adults: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06019156
Enrollment
48
Registered
2023-08-31
Start date
2022-06-13
Completion date
2023-02-10
Last updated
2023-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Brief summary

This study explored whether exercise video distribution using metaverse space is effective in increasing physical activity among young people, along with mental health and locomotive function. This is a randomized parallel-group study. Participants will be assigned to 3 groups: a metaverse group, a YouTube group, and a control group. The metaverse group will receive eight 10-minute exercise videos each week with approximately 4 to 8 METs (metabolic equivalents of task) in the metaverse space to encourage exercise, and the YouTube group will receive access to the same exercise videos as the metaverse group. The control group was given no specific instructions. The intervention period was 8 weeks, and physical activity and other items were measured before and after the intervention. These pre- and post-intervention measurements will be used to determine whether the delivery of exercise videos via Metaverse is effective in increasing physical activity in young adults.

Interventions

BEHAVIORALExercise video distribution of Metaverse

Participants received a 10-minute exercise video each week with a load of about 4 to 8 metabolic equivalents of task (METs) in the metaverse space, for eight videos delivered to encourage exercise.

BEHAVIORALExercise video distribution of YouTube

Participants view exercise videos with the same content as the metaverse group.

Sponsors

Hiroshima University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* individuals aged 18-30 at the time of obtaining consent * who owned a smartphone or computer and had internet access * who did not belong to an exercise community, such as a sports club

Exclusion criteria

* individuals who had a history of a disease that prohibited exercise * individuals whose physical activity was \> 3000 metabolic equivalents of task (METs)/week * pregnant (or possibly pregnant) women

Design outcomes

Primary

MeasureTime frameDescription
Physical activityThe pre-measurement answered the most recent week, and the post-measurement responded to the next week after the 8 weeks intervention was finished.The short form of the International Physical Activity Questionnaire Short Form was used to measure the effect of an intervention.

Secondary

MeasureTime frameDescription
Well-beingPre- and post- 8 weeks interventionThe Japanese version of the World Health Organization Five-Well-Being Index was used.
Psychological distressPre- and post- 8 weeks interventionThe 6-item Kessler Scale as a nonspecific psychological distress scale was used.
Locomotive syndrome risk testsPre- and post- 8 weeks interventionWe used the 25-question geriatric locomotive function scale.
Social capitalPre- and post- 8 weeks interventionThe social capital questions consisted of 11 items related to civic participation, social cohesion, and reciprocity, with a perfect score of 11 and higher scores indicating stronger social connections.
Quality of life (QOL)Pre- and post- 8 weeks interventionThe Japanese version of the 26-item World Health Organization QOL measure was used to assess QOL.

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026