ClinicalTrials.gg
RecruitingNCT06920862M2DI-AWMUpdated Sep 8, 2026

Multi-Modal Digital Interventions for Adolescent Weight Management

An interventional study of Multi-Modal Digital Intervention in Obesity, Adolescent, Weight Change, Body and Weight Stigma, sponsored by National Yang Ming Chiao Tung University. Recruiting at 2 sites in Taiwan. Open to participants aged 12 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-08.

Sponsored by National Yang Ming Chiao Tung University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Oct 2025; still recruiting 1 year later.
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
12 Years to 18 Years
Sex
All
01

Study summary

The goal of this randomized controlled trial is to evaluate the effectiveness of a multi-modal digital intervention, based on the Theory of Planned Behavior (TPB), in promoting healthy weight control behaviors among overweight and obese adolescents. This study also aims to reduce the risk of unhealthy weight control behaviors by leveraging artificial intelligence-driven coaching, interactive platforms, gamified applications, and real-time feedback mechanisms.

The main questions this study aims to answer are:

  1. Can a multi-modal digital intervention effectively modify adolescents' primary beliefs underlying TPB constructs (attitude, subjective norms, and perceived behavioral control)?
  2. How do TPB constructs influence weight control intentions, and how do these intentions translate into either healthy or unhealthy weight control behaviors? What role do adolescents' body image, body satisfaction, and mental health play in moderating the relationship between weight control intention and behavior?

Participants will:

  1. Be adolescents aged 12-18 years with a BMI ≥ 85th percentile.
  2. Be randomly assigned to either the intervention group (multi-modal digital intervention) or the control group (general health education).
  3. Engage in AI-driven coaching, interactive digital sessions, and gamified experiences tailored to TPB constructs.
  4. Complete biweekly sessions over a period of three months (each session lasting two hours).
  5. Receive personalized feedback and real-time monitoring through the Virti platform.
  6. Participate in follow-up assessments at one month and three months post-intervention.

Researchers will compare the intervention group to the control group to determine whether the multi-modal digital intervention leads to a higher adoption of healthy weight control behaviors and a lower prevalence of unhealthy weight control behaviors.

Read the detailed description

Adolescent obesity remains a global public health challenge with far-reaching implications for physical and psychological well-being. In Taiwan, the prevalence of overweight and obesity among adolescents aged 13-18 has exceeded 30%, mirroring trends observed worldwide. The COVID-19 pandemic has further exacerbated this issue, intensifying weight gain among youth due to disrupted routines, reduced physical activity, poor sleep hygiene, and increased consumption of energy-dense foods. Despite growing awareness and reported intentions to manage weight among adolescents, there remains a substantial gap between intention and sustained healthy behavior.

This study seeks to bridge this intention-behavior gap through the development and evaluation of a multi-modal digital intervention, grounded in the Theory of Planned Behavior (TPB). TPB posits that intention-the most proximal predictor of behavior-is influenced by three constructs: attitude, subjective norm, and perceived behavioral control. Each construct is shaped by a distinct set of beliefs, including behavioral, normative, and control beliefs. However, limited research has explored how these constructs interact to promote healthy weight control behaviors or inadvertently contribute to unhealthy practices such as meal skipping, purging, or misuse of diet pills.

Building on the PI's previous qualitative and quantitative studies validating TPB in Taiwanese adolescents with obesity, this project designs an intervention that targets these belief systems directly. The intervention integrates artificial intelligence-driven virtual coaching, virtual reality (VR)-based simulation scenarios, gamified applications, and real-time feedback and monitoring through the Virti digital platform. Each intervention module is specifically aligned with a TPB construct:

Module A (Attitude): Uses persuasive VR messages to emphasize benefits of healthy weight control (e.g., appearance, health improvement).

Module B (Subjective Norm): Reinforces perceived social support through peer modeling and family involvement.

Module C (Perceived Behavioral Control): Builds self-efficacy by offering coping strategies to overcome common barriers (e.g., dealing with food sharing, time constraints).

The intervention will be delivered biweekly over three months, with each session lasting approximately two hours. Participants will interact with the virtual nurse avatar, respond to scenario-based questions, and receive personalized feedback. Data collection will occur at baseline, one month, and three months post-intervention.

The randomized controlled trial will enroll adolescents aged 12-18 years with a BMI at or above the 85th percentile, recruited from junior and senior high schools in Taipei. Stratified randomization will ensure balanced group assignment across districts. The intervention group will receive the full TPB-based digital program, while the control group will receive standard health education.

To evaluate intervention efficacy, the study will utilize:

TPB-based questionnaires measuring belief constructs and intention,

A weight control behavior scale distinguishing healthy vs. unhealthy practices,

Standardized tools to assess body image (MBSRQ) and mental health (PHQ-A),

Anthropometric and body composition measurements.

Quantitative data will be analyzed using mixed-design ANOVA and structural equation modeling (SEM) to assess changes over time and the mediating role of psychological factors. Thematic analysis of qualitative data (collected via platform interaction and interviews) will further elucidate adolescents' experiences and the intervention's impact.

This research is expected to make a significant contribution by:

Unpacking the cognitive mechanisms that translate weight control intentions into specific behaviors,

Demonstrating how digital interventions can be effectively tailored using TPB constructs,

Offering an innovative, scalable, and theory-driven model for adolescent obesity intervention that prioritizes psychological safety, personalization, and user engagement.

Ultimately, this study aims to inform policy and practice by providing empirical evidence for the use of AI-enhanced, VR-integrated interventions to promote healthy lifestyle behaviors among adolescents-a critical population for early preventive efforts.

02

Conditions studied

  • Obesity, Adolescent
  • Weight Change, Body
  • Weight Stigma
03

In context

Pediatric Obesity

1,129 studies on the registry are indexed under Pediatric Obesity; 187 are open to participants now.

This study's planned enrollment of 200 is above the median of 100 across 870 interventional studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

National Yang Ming Chiao Tung University is the lead sponsor of 208 studies on the registry; 60 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adolescents aged 12-18 years.
  • (BMI) ≥ 85th percentile according to the Health Promotion Administration (HPA) standards.
  • Willing to participate in a digital intervention for weight control.
  • At least one parent or guardian provides consent for participation.
  • Able to understand and use digital devices (smartphones, tablets, or computers).

Exclusion criteria

Exclusion Criteria:

  • Significant communication barriers (e.g., severe speech, hearing, or cognitive impairments).
  • Psychiatric disorders that affect interpersonal interaction (e.g., schizophrenia, severe depression).
  • Previous negative experiences with digital health interventions (VR or AI-based coaching).
  • Severe motion sickness that affects the ability to use VR-based tools.
  • Currently enrolled in another weight management program that may interfere with study outcomes.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Multi-Modal Digital Intervention Group

    Participants in this group will receive a multi-modal digital intervention designed to enhance healthy weight control behaviors among overweight and obese adolescents. 1. Intervention Components: The intervention integrates AI-driven coaching, interactive platforms, gamified applications, and real-time feedback mechanisms. 2. Session Structure: Participants will complete biweekly intervention sessions (2 hours each) over a 3-month period. 3. Theoretical Framework: The intervention is grounded in the Theory of Planned Behavior (TPB) to target attitudes, subjective norms, and perceived behavioral control regarding weight control behaviors. 4. Digital Platform: Participants will have access to the Virti platform, where they will receive personalized guidance and feedback.

    Behavioral: Multi-Modal Digital Intervention

  • Active comparator
    Control Group (General Health Education)

    General Health Education sessions covering basic principles of nutrition, physical activity, and lifestyle modifications for weight management. These sessions will be delivered using traditional educational methods (e.g., brochures, videos, lectures).

    Behavioral: Multi-Modal Digital Intervention

Interventions

  • BehavioralMulti-Modal Digital Intervention

    Participants in this group will receive a multi-modal digital intervention designed to enhance healthy weight control behaviors among overweight and obese adolescents. 1. The intervention integrates AI-driven coaching, interactive platforms, gamified applications, and real-time feedback mechanisms. 2. Participants will complete biweekly intervention sessions (2 hours each) over a 3-month period. 3. The intervention is grounded in the Theory of Planned Behavior (TPB) to target attitudes, subjective norms, and perceived behavioral control regarding weight control behaviors. 4. Participants will have access to the Virti platform, where they will receive personalized guidance and feedback.

06

What researchers measure

Primary outcomes

  1. Change in Healthy Weight Control Behaviors as Measured by the Weight Control Behavior (WCB) Scale

    This outcome measures the change in healthy weight control behaviors among overweight and obese adolescents following the intervention. Healthy behaviors include increased physical activity, improved dietary habits (e.g., higher intake of fruits and vegetables), reduced consumption of sugary drinks, and portion control. Data will be collected using the healthy subscale of the Weight Control Behavior (WCB) Scale, a validated tool with a score range from 0 to 100. Higher scores reflect greater engagement in healthy weight control behaviors. Data will be analyzed as mean change from baseline at T1 and T2.

    Time frame: Baseline (T0), 1 month post-intervention (T1), 3 months post-intervention (T2)

  2. Change in Unhealthy Weight Control Behaviors as Measured by the Weight Control Behavior (WCB) Scale

    This outcome measures the change in unhealthy weight control behaviors among overweight and obese adolescents following the intervention. Unhealthy behaviors include meal skipping, fasting, using diet pills or other weight-loss supplements, and extreme restriction. Data will be collected using the unhealthy subscale of the Weight Control Behavior (WCB) Scale, a validated tool with a score range from 0 to 100. Higher scores reflect greater frequency of unhealthy behaviors. Data will be analyzed as mean change from baseline at T1 and T2.

    Time frame: Baseline (T0), 1 month post-intervention (T1), and 3 months post-intervention (T2)

Secondary outcomes

  1. Change in TPB Constructs (Attitude, Subjective Norm, and Perceived Behavioral Control) as Measured by the Theory of Planned Behavior (TPB) Questionnaire

    This outcome measures changes in three key cognitive constructs-attitude, subjective norm, and perceived behavioral control-regarding weight control behaviors among adolescents. These constructs are assessed using a validated Theory of Planned Behavior (TPB) Questionnaire, developed and tested in prior adolescent obesity studies. Each construct is measured using multiple items rated on a 7-point Likert scale (ranging from -3 = strongly disagree to +3 = strongly agree). Higher scores indicate more favorable attitudes, stronger perceived social support (subjective norm), and greater confidence in one's ability to perform weight control behaviors (perceived behavioral control). Changes will be reported as mean score differences from baseline at T1 and T2 for each construct separately.

    Time frame: Baseline (T0), 1 month (T1), and 3 months (T2) post-intervention

  2. Change in Body Mass Index (BMI)

    Body Mass Index (BMI) will be calculated using measured weight (kg) and height (m) (BMI = kg/m²). Measurements will be taken using standardized digital scales and stadiometers. Changes in BMI will be analyzed as the mean difference from baseline to post-intervention to evaluate changes in body weight status.

    Time frame: Baseline (T0) and 3 months post-intervention (T2)

  3. Change in Body Fat Mass (kg) as Measured by InBody 770

    This outcome measures changes in total body fat mass (kg) using InBody 770, a validated bioelectrical impedance analysis (BIA) device. Fat mass will be reported in kilograms, and changes will be analyzed as mean difference from baseline.

    Time frame: Baseline (T0) and 3 months post-intervention (T2)

  4. Change in Lean Body Mass (kg) as Measured by InBody 770

    This outcome assesses changes in lean body mass (kg), also measured using the InBody 770 device. Lean mass includes muscle and other non-fat tissue. Results will be reported as mean change from baseline.

    Time frame: Baseline (T0) and 3 months post-intervention (T2)

  5. Change in Body Image as Measured by the Multidimensional Body-Self Relations Questionnaire (MBSRQ)

    This outcome assesses changes in body image among adolescents using the MBSRQ, a validated instrument that evaluates multiple dimensions of body-self relations (e.g., appearance evaluation, appearance orientation). Scores from relevant subscales will be analyzed as mean score changes from baseline to post-intervention. Higher scores indicate more positive body image and greater satisfaction with one's appearance.

    Time frame: Baseline (T0) and 3 months post-intervention (T2)

  6. Change in Self-Esteem as Measured by the Multidimensional Body-Self Relations Questionnaire (MBSRQ)

    This outcome evaluates changes in self-esteem-related dimensions of body image, particularly self-classified weight and appearance orientation, as assessed by subscales of the MBSRQ. Changes will be reported as mean differences in scale scores from baseline to 3 months, where higher scores represent greater self-confidence in body-related self-perception.

    Time frame: Baseline (T0) and 3 months post-intervention (T2)

  7. Change in Depression Symptoms as Measured by the Patient Health Questionnaire for Adolescents (PHQ-A)

    This outcome examines changes in depressive symptoms using the PHQ-A, a 9-item, self-report screening tool adapted from the PHQ-9 for adolescent populations. Scores range from 0 to 27, with higher scores indicating greater severity of depressive symptoms. The primary analysis will assess mean score change from baseline to post-intervention.

    Time frame: Baseline (T0) and 3 months post-intervention (T2)

07

Study locations

1 of 2 sites recruiting
  • National Yang Ming Chiao Tung University
    Hsinchu, 300, Taiwan
    Not yet recruiting
  • National Yang Ming Chiao Tung University
    Taipei, 112, Taiwan
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — Due to ethical and confidentiality concerns, individual participant data will not be shared.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06920862
Responsible party
Pei-Ching Liu (Assistant Professor, National Yang Ming Chiao Tung University) — Principal investigator
First posted
Apr 10, 2025
Start date
Oct 31, 2025
Primary completion
Jul 31, 2028 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Sep 8, 2026

Study contacts

Peiching Liu, PhD
Contact
ressyliu@gmail.com
0928528070

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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