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We will conduct a randomized controlled trial to evaluate the effectiveness of group commitment contracts for smoking cessation and weight loss.
Full description
Initial screening will be conducted online via the Qualtrics survey platform. Respondents meeting the inclusion/exclusion criteria will immediately be randomized into one of the intervention arms described below, and then take a baseline survey. This baseline survey will also be conducted online via the Qualtrics survey platform. The initial screening, randomization, and baseline survey should take approximately 15 minutes total and can be completed anywhere the participant has an internet connection.
INTERVENTION: Respondents who meet the inclusion/exclusion criteria will be randomized into one of the following arms:
Subjects in Arms #2-4 will be cross-randomized into two subgroups:
A. Additional information treatments on the likelihood of success of the different incentives and contracts, with the goal of shifting "naives" to "sophisticates."
B. No additional information treatments.
FOLLOW-UP SURVEY: After the participants finish their contract, they will be emailed a link to the follow-up survey that will be administered online via the Qualtrics survey platform. The survey should take approximately 5 minutes and can be completed anywhere the participant has an internet connection. Participants will be directly prompted to answer whether they have been able to quit smoking or lose their target weight in the past six months. If a participant self-reports a claim of smoking cessation or successful weight loss, they will be asked to furnish at-home verification of their claim.
IN-PERSON VERIFICATION: A randomly selected subset of successful participants will be asked for in-person verification of their claim with a urine test (smoking cessation) or in-person weigh-in (weight loss) at a Quest Diagnostics location of their choice.
Enrollment
Sex
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Volunteers
Inclusion criteria
If completing a smoking cessation contract:
If completing a weight loss contract:
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
3,600 participants in 7 patient groups
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Central trial contact
Sneha Stephen, MA
Data sourced from clinicaltrials.gov
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