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OpenTrials
Completed

NCT Number: NCT02031185

A Wearable mHealth Device to Promote Teenagers' Physical Activity

Due to disparities in childhood obesity, interventions for physical activity promotion and obesity prevention for low socioeconomic and racial/ethnic minority children and adolescents are vital to address disparities across the lifespan. Mobile health applications (mHealth apps) are a rapidly growing and promising approach for interactive and individualized interventions for disease prevention. Smart phones are a promising platform to reach racial/ethnic minority and lower income groups due to high rates of adoption of smart phone usage among these groups When paired with wearable sensing devices, mHealth apps for smart phones can collect data and provide feedback to users in real time. In a study among university students regarding mHealth apps, participants expressed interest in the "ability to record and track behaviors and goals and the ability to acquire advice and information 'on the go'". For physical activity in particular, wearable physical activity monitors designed for consumers that objectively measure and display data related to an individual's physical activity on smart phones through mHealth apps have become widely available and affordable. These wearable devices wirelessly upload data and provide users with physical activity data visualization and goal setting features that can be customized for each user via internet-based applications for smart phones, tablets, and/or computers. While several internet-based behavioral programs to promote pediatric physical activity have been reported in a recent review, none examined wearable sensing devices coupled with mHealth apps. Similarly, a 2013 review on mHealth technologies for physical activity assessment and promotion reported no studies that used wearable sensing devices for intervention delivery and called for research to evaluate feasibility.

The Primary Goal is to conduct a pilot randomized controlled trial (RCT) of the FitBit Flex, a popular wearable physical activity sensing device that allows data visualization and goal setting on smart phones. The target population will be adolescents ages 14-18 years old in the Seattle-metro area (n=40) with approximately 50% from low income households or belonging to a racial/ethnic minority. We will target this older age group since they have the lowest levels of physical activity among the pediatric population. This pilot study will provide feasibility and preliminary data for a future R01-funded RCT of the Flex mHealth device and app.

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Key information

Age range

14 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Seattle Children's Research Institute

Seattle, Washington, 98145-5005, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • 14-18 years old
  • lives in the Seattle-metro area
  • able to complete forms in English
  • no restrictions by a health care provider on physical activity or walking
  • own a smart phone or similar FitBit compatible mobile device (e.g. iPod Touch)
  • agree to install and share data from the FitBit Flex smart phone app with the investigators
  • attends study high school or health clinic or receives and clicks on a Facebook advertisement for the study

Exclusion criteria

  • has been restricted by a health care provider for physical activity or walking
  • does not live in the Seattle-metro area
  • does not attend a study school or clinic, or did not receive a Facebook advertisement for the study

Treatment and study plan

Fitbit Only

Behavioral

Participants will use the FitBit device

FitBit and Text Messages

Behavioral

Participants will use the FitBit device and receive daily affective text messages

Primary outcomes

  1. Post-intervention daily steps

    Time frame: Measured during weeks 3-4 of the intervention

Secondary outcomes

  1. Pre-intervention daily steps

    Time frame: Baseline

  2. Pre-intervention moderate-to-vigorous physical activity (MVPA)

    Time frame: Baseline

    Accelerometry

  3. Post-intervention moderate-to-vigorous physical activity

    Time frame: During weeks 3-4 of the intervention

    accelerometry

Sponsors and collaborators

Lead sponsor

Seattle Children's Hospital

Other

Registry information

Official study title

A Wearable mHealth Device to Promote Teenagers' Physical Activity: A Pilot RCT

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jan 9, 2014
Registry last updated
Apr 13, 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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