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OpenTrials
Completed

NCT Number: NCT02564445

Using Social Incentives and Gamification for Weight Loss Promotion

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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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 to 70 years
  • Ability to read and provide informed consent
  • Has an iPhone 4 or newer
  • Have self-reported body mass index of 30 or greater and in-person body mass index of 28 or greater

Exclusion criteria

  • Conditions that would make participation infeasible such as inability to provide informed consent, illiteracy or inability to speak, read, and write English
  • Conditions that would make participation unsafe such as current treatment for drug or alcohol use, myocardial infarction or stroke within the last 6 months, metastatic cancer, pregnant, breastfeeding or plan to become pregnant during study period, previous diagnosis of an eating disorder, or history of unsafe weight loss practices
  • Already enrolled in another weight loss study
  • Any other medical conditions or reasons that they could not complete a 36-week weight loss program

Treatment and study plan

Gamification

Behavioral

All participants will be entered with their teammate into a game that includes points and levels

Share Data with PCP

Behavioral

Weight and step count data will be shared with the participant's primary care physician

Feedback on weight

Behavioral

Participants will use a wireless weight scale to weigh-in at home and receive feedback on weight.

Feedback on step counts

Behavioral

Participants will use a smartphone application that uses accelerometers within the phone to track step counts and receive feedback on step counts

Primary outcomes

  1. Change in weight in pounds

    Time frame: 24-week primary intervention period

Secondary outcomes

  1. Change in weight in pounds

    Time frame: 12-week follow-up period

  2. Physical activity (mean daily steps)

    Time frame: 24-week primary intervention period

  3. Physical activity (mean daily steps)

    Time frame: 12-week follow-up period

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Registry information

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Sep 30, 2015
Registry last updated
Dec 21, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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