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Metaverse-Based Healthy Life Program for Youth

The Effect of Metaverse-Based Healthy Life Program on Risk Reduction of Non-Communicable Diseases in Youth

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05332886
Acronym
MetaYouth
Enrollment
600
Registered
2022-04-18
Start date
2024-07-01
Completion date
2025-05-01
Last updated
2022-04-18

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

Conditions

Health-Related Behavior, Health Risk Behaviors, Healthy Eating Index, Healthy Lifestyle, Healthy Nutrition, Non Communicable Diseases, Physical Inactivity, Stress, Emotional

Brief summary

This study was planned within the scope of the call titled Non-communicable diseases risk reduction in adolescence and youth (Global Alliance for Chronic Diseases - GACD) with identity number HORIZON-HLTH-2022-DISEASE-07-03. The purpose of this project; is to determine the effect of the Metaverse-Based Healthy Life Program to be developed in the project to support youths in decreasing future risks of developing non-communicable diseases (NCDs) and in gaining healthy lifestyle behaviors (HLBs).

Detailed description

The project consists of three phases. Phase 1 Testing the content, quality, reliability, and usability of the Metaverse-Based Healthy Life Program for Youth to be developed within the scope of the project Phase 2 Identifying youth at high risk of chronic non-communicable diseases in the research population Phase 3 Evaluating the effect of Metaverse-Based Healthy Life Program for Youth implementation on inculcating healthy lifestyle behaviors in youth

Interventions

BEHAVIORALMetaHealth Group

Three metaverse rooms will be created via metaverse technology that aims to develop healthy nutrition, physical activity, and psychological resilience skills to reduce the risk of of NCDs in youth.

BEHAVIORALMobileHealth Group

The intervention aims to develop healthy nutrition, physical activity, and psychological resilience skills using mobile application materials to reduce the risk of NCDs in youth.

Sponsors

Horizon
CollaboratorINDUSTRY
Ayşegül İşler Dalgıç
Lead SponsorOTHER

Study design

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

Masking description

In the study, there will be interventions in both groups, as metaverse-based education and activity programme will be given to the MetaHealth Group and digital health education with a mobile application materials will be given to the MobileHealth Group. In both groups, the participants will be aware that an attempt has been made on them, but since they will not know which group they are in, the participant will be blinded. Since the interventions will be managed by the research team, researcher blinding will not be possible. However, the statistician will be blinded. At the end of the research, the groups will be coded as A and B. Statistical analysis will be made by the statistics expert who is blinded to the groups in the project partner company. After the statistical analysis are made and the research report is written, the situations expressed by A and B will be explained to the statistician. In this way, it is planned to control the bias in statistics and reporting.

Intervention model description

Parallel Desing Active Comparative Group Randomized Controlled Trial

Eligibility

Sex/Gender
ALL
Age
15 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

* Being a university student in the project partner countries and not older than 24, * Having a score of 130 or lower on the HLBS II in the first stage of the research, * Determining that BMI ≥ 25-34.99 kg/m2 in the first stage of the research and * Using a smartwatch during the research, * Accepting to participate in the research voluntarily

Exclusion criteria

* Having chronic diseases (asthma, diabetes, heart, kidney failure, hypertension, cancer, etc.) * Those who have a drug that they use constantly * Having a psychiatric diagnosis (depression, anxiety, bipolar disorder, schizophrenia, etc.) * Having a disease that prevents the use of metaverse (vertigo, vision, hearing, etc.)

Design outcomes

Primary

MeasureTime frameDescription
Healthy Lifestyle Behavior Scale II (HLBS II)The HLBS II score will evaluate at baselineThe HLBS II consists of 52 items in total and has 6 sub-factors. Sub-factors are spiritual growth, health responsibility, physical activity, nutrition, interpersonal relationships, and stress management. All items on the scale are positive. The rating is in the form of a 4-point Likert. Never (1), sometimes (2), often (3), regularly (4). The lowest score for the whole scale is 52, and the highest score is 208. The Cronbach Alpha reliability coefficient of the scale is 0.94.
International Physical Activity Questionnaire-Short Form (IPAQ-SF)The IPAQ-SF score will evaluate at baselineThe IPAQ-SF is a standardized questionnaire prepared to measure the physical activity of people between the ages of 15 and 65. In the survey, there are 7 questions in total in 4 separate sections about the activities that have been done for a minimum of 10 minutes in the last 7 days. The results obtained in the assessment are calculated as metabolic equivalent task (MET) - min/week.
Positive and Negative Affect Schedule (PANAS-SF)The PANAS-SF score will evaluate at baselineThe PANAS-SF is a self-report questionnaire that consists of two 10-item scales to measure both positive and negative affect. Each item is rated on a 5-point scale of 1 (not at all) to 5 (very much).

Countries

Turkey (Türkiye)

Contacts

Primary ContactAyşegül ISLER DALGIC, Professor
aisler@akdeniz.edu.tr+90 242 310 6103

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026