New treatment option for Tobacco-Related Carcinoma
Official title A Novel Mobile Health Intervention for Improving Tobacco Cessation Among Young Adults
ClinicalTrials.gov ID: NCT07571018
What this study is testing
- What it's testing
- Tobacco use is the leading cause of preventable cancer deaths. Among young adults, approximately 1 in 5 use commercial nicotine and tobacco products, putting them at risk of developing nicotine addiction and long-term health effects from exposure to toxicants.
- Time commitment: about 1 week
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 30. Healthy volunteers may be eligible.
You may be able to join if
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-identify being between 18 and 30 years of age
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must be a United States (US) resident, with a US mailing address
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report use of any (non-therapeutic) nicotine or tobacco product at least once...
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must own a smartphone
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report having internet access for the interviews
You likely can't join if
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Individuals must not be \ 30 years of age
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Individuals must not have a Google voice number as their sole phone number
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Individuals who are non-English speaking cannot participate, as this would prevent their participation...
- PILOT TRIAL: Participants must not be \ 30 years of age
- PILOT TRIAL: Participants must not be currently using other tobacco cessation treatments at the time of screening, including pharmacotherapy or...
- PILOT TRIAL: Participants must not be a member of the same household as another research participant
See the full eligibility criteria
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-identify being between 18 and 30 years of age
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must be a United States (US) resident, with a US mailing address
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report use of any (non-therapeutic) nicotine or tobacco product at least once per week in the 30 days prior to screening
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must own a smartphone
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report having internet access for the interviews
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report that they are interested in participating in the study for themselves (versus [vs] someone else)
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report that they have not participated in one of our prior tobacco cessation studies
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report that they understand and agree to the conditions of compensation
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must self-report that they are not currently incarcerated
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Participants must be willing and able to complete study procedures in English
- PILOT TRIAL: Participants must self-identify being between 18 and 30 years of age
- PILOT TRIAL: Participants must currently reside in the US and anticipate continued residence for the duration of the study (3 months)
- PILOT TRIAL: Participants must self-report use of any (non-therapeutic) nicotine or tobacco product at least once per week in the 30 days prior to screening
- PILOT TRIAL: Participants must own an Android (running version 12 or higher) or iPhone (running iOS version 17 or higher, iPhone 11 or more recent)
- PILOT TRIAL: Participants must self-report having at least weekly internet access for the next three months
- PILOT TRIAL: Participants must be willing and able to download an app to their phone and receive text messages
- PILOT TRIAL: Participants must self-report current use of a personal email account
- PILOT TRIAL: Participants must self-report current use of text messaging
- PILOT TRIAL: Participants must self-report that they are interested in participating in the study for themselves (vs someone else)
- PILOT TRIAL: Participants must self-report that they have not participated in one of our prior tobacco cessation studies
- PILOT TRIAL: Participants must self-report that they understand and agree to the conditions of compensation
- PILOT TRIAL: Participants must self-report that they are not currently incarcerated
- PILOT TRIAL: Participants must be willing to use the assigned intervention program, complete the study assessments, and complete an online consent form in English
- POST PILOT TRIAL DIARY STUDY: Participants must self-identify being between 18 and 30 years of age
- POST PILOT TRIAL DIARY STUDY: Participants must currently reside in the US
- POST PILOT TRIAL DIARY STUDY: Participants must self-report use of any (non-therapeutic) nicotine or tobacco product at least once per week in the 30 days prior to screening
- POST PILOT TRIAL DIARY STUDY: Participants must own an Android (running version 12 or higher) or iPhone (running iOS version 17 or higher, iPhone 11 or more recent)
- POST PILOT TRIAL DIARY STUDY: Participants must self-report having at least internet access for the duration of the diary study
- POST PILOT TRIAL DIARY STUDY: Participants must be willing and able to download an app to their phone and receive text messages
- POST PILOT TRIAL DIARY STUDY: Participants must self-report current use of a personal email account
- POST PILOT TRIAL DIARY STUDY: Participants must self-report current use of text messaging
- POST PILOT TRIAL DIARY STUDY: Participants must self-report that they are interested in participating in the study for themselves (vs someone else)
- POST PILOT TRIAL DIARY STUDY: Participants must self-report that they have not participated in one of our prior tobacco cessation studies
- POST PILOT TRIAL DIARY STUDY: Participants must self-report that they understand and agree to the conditions of compensation
- POST PILOT TRIAL DIARY STUDY: Participants must self-report that they are not currently incarcerated
- POST PILOT TRIAL DIARY STUDY: Participants must be willing to use the intervention program, complete the study assessments, and complete an online consent form in English
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Individuals must not be \ 30 years of age
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Individuals must not have a Google voice number as their sole phone number
- USER-CENTERED DESIGN AND PROGRAM DEVELOPMENT: Individuals who are non-English speaking cannot participate, as this would prevent their participation in the interviews, which will be conducted in English
- PILOT TRIAL: Participants must not be \ 30 years of age
- PILOT TRIAL: Participants must not be currently using other tobacco cessation treatments at the time of screening, including pharmacotherapy or behavioral support (but initiating these treatments during the study is...
- PILOT TRIAL: Participants must not be a member of the same household as another research participant
- PILOT TRIAL: Participants must not have a Google voice number as their sole phone number
- PILOT TRIAL: Participants must not be identified as fraudulent per our fraud prevention protocol
- PILOT TRIAL: Participants must not be pregnant or plan on becoming pregnant over the next 3 months
- POST PILOT TRIAL DIARY STUDY: Individuals must not be \ 30 years of age
- POST PILOT TRIAL DIARY STUDY: Participants must not have a Google voice number as their sole phone number
- POST PILOT TRIAL DIARY STUDY: Individuals who are non-English speaking cannot participate, as this would prevent their participation in the interviews, which will be conducted in English
The study team makes the final eligibility decision.
Where it's taking place
- Las Cruces, New Mexico, United States
- Seattle, Washington, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 1 week per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 30 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Las Cruces, New Mexico, United States; Seattle, Washington, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.