Partnering With Food Bank to Provide Tobacco Treatment to Underserved Smokers

H. Lee Moffitt Cancer Center and Research Institute502 enrolled

Overview

This study will evaluate the efficacy and economic impact of a theoretically-based, fully automated, interactive smartphone-based smoking cessation intervention.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Enrollment

502

Conditions

Smoking Cessation

Interventions

Smartphone-delivered automated treatmentBEHAVIORAL

An interactive smartphone-based intervention that comprises content delivered via audio/video clips and text content automatically each week for 12 weeks and on demand for 26 weeks to participants

Nicotine patchDRUG

Participants will be provided with a 10-week supply of nicotine patches

CounselingBEHAVIORAL

Smoking cessation treatment delivery by State Quitline's

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * ≥100 lifetime cigarettes * English or Spanish speaking * Currently smoke ≥5 cigarettes/day * Process a smartphone compatible with the project app * Have a valid email address * Receipt of food assistance in the past 3 month Exclusion Criteria: * Currently pregnant or breastfeeding * Current use of smoking cessation medications * Enrolled in a smoking cessation study * Household member enrolled in the study * Failure to electronically confirm participation with 14 days of randomization via electronic link sent to participant's smartphone

Locations (1)

Moffitt Cancer Center

Tampa, Florida, United States

Outcomes

Primary Outcomes

Self-Reported 7-Day Point-Prevalence Smoking Abstinence

Participants who report no smoking, not even a puff, within the past 7 days

Time frame: 12 Month Follow-Up

Secondary Outcomes

Biochemical Verification Via Salivary Cotinine

Investigators will biochemically verify smoking status by collecting cotinine samples via salivary cotinine kit

Time frame: 12 Month Follow-Up

Self-Reported 24-Hour Point-Prevalence Smoking Abstinence

Number of participants who report no smoking, not even a puff, within the past 24 hours

Time frame: 12 Month Follow-Up

Self-Reported 30-Day Point-Prevalence Smoking Abstinence

Number of participants who report no smoking, not even a puff, within the past 30 days

Time frame: 12 Month Follow-Up

Data from ClinicalTrials.gov

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