- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02932917
MapMySmoke: Smoking Cessation App With Geospatial Capture
MapMySmoke: Feasibility of a New Quit Cigarette Smoking Mobile Phone Application Using Integrated Geo-positioning Technology, and Motivational Messaging Within Primary Care Setting
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Investigators know that place-based cues play an important role in the triggering of smoking events, and even in relapse events. It follows that providing individual smokers with spatially explicit and temporally dynamic intervention messages may support smoking cessation attempts.
The investigators have built a mobile phone application-MayMySmoke-that allows individuals to capture each smoking event at the times and places they occur, and tag the events with qualitative metadata. The app also allows individuals to document and describe craving events. The goal of the app is first to understand an individual's smoking profile, and second to support them with dynamic text messages.
The investigators are deploying the app in a clinical setting-the United Kingdom's National Health Service, within the Fife region of Scotland. Using two feasibility studies of increasing size, the investigators are attempting first to get initial feedback on the app, and then to improve the app and deploy it across a broader community of smokers.
Though the app is targeted to smoking behavior, it is possible to extend it to include other negative health behaviors that may have a spatial component.
Study Type
Enrollment (Anticipated)
Phase
- Phase 1
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- National Health Service (Fife) Patients
- Self-reported tobacco smoker
- Stated intention to quit smoking
- English speaker
Exclusion Criteria:
- Mental illness
- learning difficulty
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: MapMySmoke
All patients in the study will use the MapMySmoke app to document their smoking and craving behavior
|
Each patient in the study arm will download and install the MapMySmoke app to record all of their smoking and craving events.
The app will generate a quantitative summary of their smoking behavior during a pre-quit phase, and will provide dynamic text support messages during the post-quit phase.
The app will also capture spatial details of any relapse events during the post-quit phase.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Continued use of the MapMySmoke App as Assessed by Monitoring Individual Anonymized Data Feeds on the Server
Time Frame: 1 year
|
The investigators will determine, via the data feed to the server, if patients continue to use the app during the pre- and post-quit phase
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of Patients Using the App Who Are Abstinent from Smoking As Assessed by Follow-up Survey
Time Frame: 4 weeks
|
The investigators will determine via survey if patients have maintained their quit attempt
|
4 weeks
|
Number of Patients Using the App Who Are Abstinent from Smoking As Assessed by Follow-up Survey
Time Frame: 3 months
|
The investigators will determine via survey if patients have maintained their quit attempt
|
3 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Robert S Schick, PhD, University of St Andrews
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- XAP062
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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