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OpenTrials
Completed

NCT Number: NCT02116283

Mobile Sensing of Smoking Behavior

Smokers will use a smartphone app on a smartphone provided for the study that will passively sense and record information about their activities. Information collected from the smartphone app will be used to develop future smartphone apps that will predict when an individual is at risk of smoking.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Duke University Medical Center

Durham, North Carolina, 27705, United States

About this study

Smokers will carry an Android-based smartphone, which they are to use as their own for one month. After using the smartphone for two weeks, they will abstain from smoking for 48 hours. The phone will passively sense and record information from onboard sensors and send that information to a central server. When server based algorithms detect a pattern of signals likely associated with smoking behavior, the smoker will be queried regarding their current state (smoking?, not smoking but likely to in the next 10 minutes?, etc.). Likewise, when smokers are about to smoke but were not queried, they can indicate they are about to smoke. This information will be used to update algorithms using machine learning techniques. As such, in this study investigators will gain knowledge that will increase understanding of antecedents of smoking behavior and improve the accuracy with which smoking risk can be detected.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • generally healthy
  • between the ages of 18 and 65
  • smoking of at least 10 cig/day of a brand delivering ≥ 0.5 mg nicotine (FTC method) for > 1 year AND an afternoon expired CO concentration >5 ppm (to confirm inhalation) or morning urinary cotinine > 100 ng/mL
  • willingness to carry and use a study smartphone as their own for one month

Exclusion criteria

  • inability to attend all required sessions
  • use of smokeless tobacco products
  • current use of nicotine replacement therapy or other smoking cessation treatment

Treatment and study plan

48 hour smoking abstinence

Behavioral

Participants will maintain smoking abstinence for 48 hours

Smartphone

Other

Participants will use an Android-based smartphone as their own for one month

Primary outcomes

  1. Change in smoking behaviors as measured by an algorithm of social variables

    Time frame: up to 4 weeks

    phone calls (time, duration, coded identity of contact, including smoking status); SMS texting (time sent, coded identity of contact)

Secondary outcomes

  1. Change in smoking behaviors as measured by an algorithm of motion variables

    Time frame: up to 4 weeks

    acceleration; direction and magnitude of gravity; device orientation

  2. Change in smoking behaviors as measured by an algorithm of environmental variables

    Time frame: up to 4 weeks

    light; proximity; magnetic field; pressure; temperature

  3. Change in smoking behaviors as measured by an algorithm of device interaction variables

    Time frame: up to 4 weeks

    running applications; applications installed; screen status

  4. Change in smoking behaviors as measured by an algorithm of positioning variables

    Time frame: up to 4 weeks

    location; Bluetooth devices within range; available WiFi access points; ID for the current cell tower the device is connected to

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Acronym: Mobi-Smoke

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Apr 16, 2014
Registry last updated
Nov 5, 2014

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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