UPCC 08024 Remote Vs. In-Person Study Evaluation (RISE) Trials: RISE Above Smoking (Trial 1)
Brief description of study
The purpose of this study is to learn about differences between in-person and/or remote visits designed to help people to quit smoking with a combination of nicotine replacement patches and lozenges. We aim to compare the remote and in-person groups based on their accrual and retention rates as well as other key metrics of trial quality. We will also examine the impact of trial efficiency and quality on sub-groups that experience health inequities.
Detailed description of study
If you agree to join the study you will be asked to:
- Attend 1 Intake session which will last about 1 hour
- Attend 5 Treatment and Assessment sessions which are 30-60 minutes each
- At each Treatment and Assessment session you will provide a breath sample, complete surveys about your experiences, and review your smoking behavior and medication usage
Use the 8 weeks of combination nicotine replacement therapy (patch and lozenge) that we will provide to you
Whether your visits are remote or in-person will be determined randomly by a computer
program.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Clinical Research
-
Age: 18 years - 99 years
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Gender: All
Please choose between Voice or SMS based delivery of verification code
or