Gamification
BehavioralAll participants will be entered with their teammate into a game that includes points and levels
NCT Number: NCT02564445
This is a 36-week, three-arm randomized, controlled trial using a team-based model to compare two weight loss programs to control. Each intervention will use insights from behavioral economics to leverage social incentives and gamification.
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Notify Me18 year–70 year
All sexes
Interventional
Phase 3
Obesity is a leading risk factor for morbidity and mortality affecting more than one in three adults in the United States. Modifiable health behaviors contribute to this growing epidemic. Insights from behavioral economics have shown promise for motivating behavior change through the use of financial incentives. However, social incentives or those influences that impact individuals to adjust their inherent behaviors based on social ties and connections have not been well examined. Social incentives are a more patient-centered approach that leverages and enhances the existing connections and influences on the individual. Since one individual's behavior change is connected to many others within their network, social incentives have the potential to be a scalable intervention that impacts the community. Gamification, or the use of game design in non-game situations, is often used in the real world, but its effectiveness is unknown. In this study, investigators will conduct a 36-week, three-arm, randomized, controlled trial using a team-based model to compare two weight loss programs to control. Each intervention will use insights from behavioral economics to leverage social incentives and gamification.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
All participants will be entered with their teammate into a game that includes points and levels
Weight and step count data will be shared with the participant's primary care physician
Participants will use a wireless weight scale to weigh-in at home and receive feedback on weight.
Participants will use a smartphone application that uses accelerometers within the phone to track step counts and receive feedback on step counts
Time frame: 24-week primary intervention period
Time frame: 12-week follow-up period
Time frame: 24-week primary intervention period
Time frame: 12-week follow-up period
University of Pennsylvania
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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