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WAVE~Ripples for Change: Obesity Prevention in Active Youth

The WAVE~Ripples for Change: Obesity Prevention in Active Youth in Afterschool Programs Using Virtual- and Real-World Experiential Learning

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03215485
Enrollment
498
Registered
2017-07-12
Start date
2014-08-31
Completion date
2018-12-31
Last updated
2022-04-04

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

Conditions

Childhood Obesity Prevention

Keywords

adolescent, sports, nutrition, physical activity, body mass index, virtual world

Brief summary

Intervention targets youth ages 14 - 19 participating in soccer teams. The intervention group will be given face to face nutrition lessons and have access to an online immersive learning environment. The comparison group will not. The project will test if the immersive learning environment is effective in preventing unhealthy weight gain.

Detailed description

Active youth are just as likely to develop poor dietary habits that can contribute to obesity later in life, after high school sports has ended. However, youth in sports may provide a key window of opportunity to teach them about eating health foods if that information is tied to sport performance. This project will test to see if that is true. The virtual world is an idea medium for learning for this project. The project will test whether it indeed can result in behavior change more effectively than just more traditional face to face learning.

Interventions

BEHAVIORALNutrition lessons

Face-to-face interactive group lessons delivered in the classroom.

BEHAVIORALVirtual world learning environment

Every participant has their own unique avatar in the virtual world learning environment named Rippleville. They can choose to complete quests, watch archived nutrition video lessons, explore, and socialize with other avatars. They receive rewards (Rippleville dollar and badges) for their efforts.

All participants in the intervention and comparison groups receive up to 10 professional newsletters on topics related to sports nutrition and performance, healthy eating and active living tips.

Sponsors

Oregon State University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

There is one intervention group and one comparison group.

Eligibility

Sex/Gender
ALL
Age
14 Years to 19 Years
Healthy volunteers
No

Inclusion criteria

* youth ages 14 - 19 at baseline * enrolled in a high school soccer program * living with a parent/caregiver in Oregon * without medical condition that hinders them from consuming normal healthy diets * has assess to the internet during the 2-year study * proficient in English

Exclusion criteria

* non-English speakers (youth) * prisoners

Design outcomes

Primary

MeasureTime frameDescription
Nutrition: Meet specific good groups dietary recommendation/guideline for fruit, vegetables, fat, and sugar intakes.Change from baseline at 12 and 24 months laterIntakes of fat, sugar, fruits and vegetables are measured by self-reported screener using the Block Food Frequency Questionnaires (FFQ). Change in intake frequencies are compared baseline, 12 and 24 months later.
Physical activity: Meet moderate to vigorous physical activity (MVPA) recommendation.Change from baseline at 12 and 24 months laterMVPA is measured by total steps and minutes per day with the use of a wearable lifestyle tracker such as the Fitbit. Average steps during soccer season and outside soccer season are compared.
Sleep about 8 hours/day.Change from baseline at 12 and 24 months laterTogether with MVPA, sleep is measured by average number of sleep hours per day as self-reported by participants via written and/or electronic surveys .

Secondary

MeasureTime frameDescription
Growth-adjusted Body Mass Index (kg/m2)Change from baseline at 12 and 24 months laterHeight and body weight are measured using a stadiometer (SECA 217, SECA Corp., Singapore) and a Tanita scale (TM-300A, Tanita Corp., Itabashi-Ku, Tokyo, Japan).

Outcome results

None listed

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