- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01746472
Study of the Diffusion of a Smoking Cessation Application Through an Online Network
March 14, 2016 updated by: Truth Initiative
Online Social Networks for Dissemination of Smoking Cessation Interventions
Effective evidence-based interventions exist for smoking cessation delivered over the Internet, but consumer acceptance and adherence remains low.
Scalable and efficient mechanisms to disseminate these interventions online are needed, and existing online social networks provide a potential mechanism.
This is a proposal for a randomized, factorial trial of the dissemination of an evidence-based intervention through the massive Facebook social network, with the goal of determining intervention characteristics that drive viral spread.
Study Overview
Status
Completed
Study Type
Interventional
Enrollment (Actual)
11413
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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District of Columbia
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Washington, District of Columbia, United States, 20001
- Truth Initiative
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Facebook user
- Age 18 years or older
- Entered UbiQUITous Facebook Application
- Confirms smoker status
- U.S. resident
Exclusion Criteria:
- Non-smoker
- Under 18 years old
- Non-U.S. resident
- Non-Facebook advertisement point of entry
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: 2 - B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
|
Experimental: 3 - B-active
|
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
|
Experimental: 4 - B-active, B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
|
Experimental: 6 - z, B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
Application components hypothesized to increase the number of friends that a user has that are eligible to install the application.
|
Experimental: 7 - z, B-active
|
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
Application components hypothesized to increase the number of friends that a user has that are eligible to install the application.
|
Experimental: 8 - z, B-active, B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
Application components hypothesized to increase the number of friends that a user has that are eligible to install the application.
|
Experimental: 10 - t, B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
Application components hypothesized to increase the duration (t, time) that a participant spends using the application.
|
Experimental: 11 - t, B-active
|
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
Application components hypothesized to increase the duration (t, time) that a participant spends using the application.
|
Experimental: 12 - t, B-active, B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
Application components hypothesized to increase the duration (t, time) that a participant spends using the application.
|
Experimental: 14 - t, z
|
Application components hypothesized to increase the number of friends that a user has that are eligible to install the application.
Application components hypothesized to increase the duration (t, time) that a participant spends using the application.
|
Experimental: 15 - t, z, B-active
|
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
Application components hypothesized to increase the number of friends that a user has that are eligible to install the application.
Application components hypothesized to increase the duration (t, time) that a participant spends using the application.
|
Experimental: 16 - t, z, B-active, B-passive
|
Application components hypothesized to increase the contagiousness of the app by increasing the passive diffusion of information from the user to their friends.
Other Names:
Application components hypothesized to increase the contagiousness of the app by increasing a users ability and desire to proactively contact others.
Other Names:
Application components hypothesized to increase the number of friends that a user has that are eligible to install the application.
Application components hypothesized to increase the duration (t, time) that a participant spends using the application.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Reproductive rate
Time Frame: 30 days
|
The investigators will measure the reproductive rate for each condition, in other words the average number of additional individuals that install the application for each original individual recruited to participate.
Higher reproductive rates indicate more efficient and faster dissemination.
|
30 days
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2012
Primary Completion (Actual)
October 1, 2013
Study Completion (Actual)
October 1, 2014
Study Registration Dates
First Submitted
December 3, 2012
First Submitted That Met QC Criteria
December 10, 2012
First Posted (Estimate)
December 11, 2012
Study Record Updates
Last Update Posted (Estimate)
March 15, 2016
Last Update Submitted That Met QC Criteria
March 14, 2016
Last Verified
March 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- 1R01CA155369-01A1 (U.S. NIH Grant/Contract)
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.
Clinical Trials on Cessation of Smoking
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-
University of Southern CaliforniaAmerican Cancer Society, Inc.CompletedSmoking | Smoking Cessation | Smoking, Cigarette | Smoking Behaviors | Cessation, SmokingUnited States
-
Nabi BiopharmaceuticalsNational Institute on Drug Abuse (NIDA)CompletedSmoking | Smoking Cessation | Tobacco CessationUnited States
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-
Claremont Graduate UniversityNational Cancer Institute (NCI)CompletedSmoking | Smoking Cessation | Tobacco Use | Tobacco Smoking | Tobacco Use Cessation | Smoking, CigaretteUnited States
-
Memorial University of NewfoundlandCompletedSmoking Cessation | Quality of Life | Smoking, TobaccoCanada
-
Heidelberg UniversityPfizerTerminatedSmoking | Smoking Cessation | Tobacco Use CessationGermany
-
Mayo ClinicNational Institute on Drug Abuse (NIDA)CompletedSmoking | Smoking Cessation | Tobacco Use | Tobacco Smoking | Tobacco Use Cessation | Smoking, Tobacco | Smoking, CigaretteUnited States
-
University of MiamiFlorida Department of HealthRecruitingSmoking Cessation | Tobacco Smoking | Tobacco Use CessationUnited States
-
The University of Hong KongNot yet recruitingSmoking Cessation Counseling Ability | Smoking Cessation Counseling PracticeHong Kong
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University of MiamiCompletedSocial Isolation | Social Support (Formal and Informal) | Well-being/Quality of LifeUnited States
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Boston Children's HospitalHarvard School of Public Health (HSPH)Completed
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