Completed

Quit4Health: Expanding the Reach of an Innovative Tobacco Control Program for Young Adults

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What is being tested

Educational Intervention

+ Questionnaire Administration

+ Smoking Cessation Intervention

OtherBehavioral
Who is being recruted

Cigarette Smoking+2

+ Tobacco Smoking

+ Behavior

From 18 to 35 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: December 2018
See protocol details

Summary

Principal SponsorM.D. Anderson Cancer Center
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 10, 2018

Actual date on which the first participant was enrolled.

PRIMARY OBJECTIVES: I. To evaluate whether smokers randomized to Quit4Health are more likely to quit smoking and remain tobacco-free at 6 months than subjects randomized to the education only control group. II. To evaluate whether non-smokers who are randomized to Quit4Health are less likely to initiate tobacco usage and remain tobacco-free at 6 months than non-smokers randomized to the education only control group. SECONDARY OBJECTIVES: I. To evaluate whether well-established predictors of susceptibility and barriers to cessation (e.g. self-efficacy, knowledge about associated risks, normative beliefs, attitudes, resistance skills, peer pressure) and recently identified predictors of tobacco use (e.g., depression, nicotine dependence, alcohol use, risk-taking propensity) will mediate the effect of the intervention on both onset (for non-smokers) and cessation (for smokers) of tobacco use. II. To evaluate whether, at the end-of-treatment (EOT) assessment, participants (both smokers and non-smokers) in Quit4Health will report a significantly better perception of Quit4Health (message relevance, tailoring to specific needs based on tobacco use status, motivation to quit, etc.) compared with their counterparts in the education only control arm. OUTLINE: Participants are randomized to 1 of 2 groups. GROUP I: Participants utilize Quit4Health intervention that includes interactive features, coping strategies and games related to cigarettes and other tobacco products for 1 month. GROUP II: Participants read an educational booklet about cigarettes and other tobacco products for 1 month. After completion of study, participants are followed at 3 and 6 months.

Official TitleQuit4Health: Expanding the Reach of an Innovative Tobacco Control Program for Young Adults
NCT04009590
Principal SponsorM.D. Anderson Cancer Center
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

579 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 35 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cigarette SmokingTobacco SmokingBehaviorSmokingTobacco Use

Criteria

7 inclusion criteria required to participate
Be enrolled in at least one class at Houston Community College (HCC) Central campus, West Loop campus or Spring Branch campus (cessation and prevention/advocacy groups)

Speak and read English (cessation and prevention/advocacy groups)

Own an Android or iOS smartphone (cessation and prevention/advocacy groups)

Provide current and relevant contact information (cessation and prevention/advocacy groups)

Show More Criteria

1 exclusion criteria prevent from participating
People who score 16 or above on the Center for Epidemiologic Studies Depression (CESD) thus showing evidence of major depressive disorder (cessation and prevention/advocacy groups)

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator
Participants read an educational booklet about cigarettes and other tobacco products for 1 month.

Group II

Experimental
Participants utilize Quit4Health intervention that includes interactive features, coping strategies and games related to cigarettes and other tobacco products for 1 month.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

M D Anderson Cancer Center

Houston, United StatesOpen M D Anderson Cancer Center in Google Maps
CompletedOne Study Center
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