Multi-Modal Digital Interventions for Adolescent Weight Management (M2DI-AWM)

April 6, 2026 updated by: Pei-Ching Liu, National Yang Ming Chiao Tung University

Effectiveness of Multi-Modal Digital Interventions for Adolescent Weight Management: A Randomized Controlled Trial

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.

Study Overview

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.

Study Type

Interventional

Enrollment (Estimated)

200

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Hsinchu, Taiwan, 300
        • Not yet recruiting
        • National Yang Ming Chiao Tung University
        • Contact:
    • Taiwan
      • Taipei, Taiwan, Taiwan, 112
        • Recruiting
        • National Yang Ming Chiao Tung University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Adolescents aged 12-18 years.
  • Body Mass Index (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:

  • 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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
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.

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.
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).

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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Healthy Weight Control Behaviors as Measured by the Weight Control Behavior (WCB) Scale
Time Frame: Baseline (T0), 1 month post-intervention (T1), 3 months post-intervention (T2)

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.

Baseline (T0), 1 month post-intervention (T1), 3 months post-intervention (T2)
Change in Unhealthy Weight Control Behaviors as Measured by the Weight Control Behavior (WCB) Scale
Time Frame: Baseline (T0), 1 month post-intervention (T1), and 3 months post-intervention (T2)

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.

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

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in TPB Constructs (Attitude, Subjective Norm, and Perceived Behavioral Control) as Measured by the Theory of Planned Behavior (TPB) Questionnaire
Time Frame: Baseline (T0), 1 month (T1), and 3 months (T2) post-intervention

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.

Baseline (T0), 1 month (T1), and 3 months (T2) post-intervention
Change in Body Mass Index (BMI)
Time Frame: Baseline (T0) and 3 months post-intervention (T2)

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.

Baseline (T0) and 3 months post-intervention (T2)
Change in Body Fat Mass (kg) as Measured by InBody 770
Time Frame: Baseline (T0) and 3 months post-intervention (T2)

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.

Baseline (T0) and 3 months post-intervention (T2)
Change in Lean Body Mass (kg) as Measured by InBody 770
Time Frame: Baseline (T0) and 3 months post-intervention (T2)

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.

Baseline (T0) and 3 months post-intervention (T2)
Change in Body Image as Measured by the Multidimensional Body-Self Relations Questionnaire (MBSRQ)
Time Frame: Baseline (T0) and 3 months post-intervention (T2)

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.

Baseline (T0) and 3 months post-intervention (T2)
Change in Self-Esteem as Measured by the Multidimensional Body-Self Relations Questionnaire (MBSRQ)
Time Frame: Baseline (T0) and 3 months post-intervention (T2)

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.

Baseline (T0) and 3 months post-intervention (T2)
Change in Depression Symptoms as Measured by the Patient Health Questionnaire for Adolescents (PHQ-A)
Time Frame: Baseline (T0) and 3 months post-intervention (T2)

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.

Baseline (T0) and 3 months post-intervention (T2)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2025

Primary Completion (Estimated)

July 31, 2028

Study Completion (Estimated)

December 31, 2029

Study Registration Dates

First Submitted

March 12, 2025

First Submitted That Met QC Criteria

April 2, 2025

First Posted (Actual)

April 10, 2025

Study Record Updates

Last Update Posted (Actual)

April 13, 2026

Last Update Submitted That Met QC Criteria

April 6, 2026

Last Verified

April 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Due to ethical and confidentiality concerns, individual participant data will not be shared.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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