Actively Recruiting

Phase Not Applicable
Age: 14Years - 24Years
All Genders
Healthy Volunteers
ID06754215

Development of a Contextually Tailored and Optimized Smoking Cessation Intervention for Homeless Youth

Led by Ohio State University Comprehensive Cancer Center ยท Updated on 2025-02-07

298

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

O

Ohio State University Comprehensive Cancer Center

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying smoking cessation among homeless youth aged 14 to 24 years who smoke cigarettes. The study aims to develop a tailored and optimized program to help homeless young people stop smoking by understanding their motivations to smoke and to quit. This research involves creating a theoretical framework that considers the unique challenges and opportunities faced by homeless youth in quitting smoking. The study includes multiple steps: a one-hour semi-structured interview and a survey to build the theoretical model, focus groups to identify and assess possible intervention components, and a feasibility study to evaluate how these components can be implemented alongside homeless youth services. All steps focus on behavioral and other related interventions designed specifically for this population. Participants will be involved in interviews, surveys, focus groups, and a feasibility study over a period of up to three years. Researchers will assess participants' psychological and physical capacity as well as physical and social factors influencing their ability to quit smoking. The study tracks these outcomes to guide future smoking cessation programs for homeless youth and monitors feasibility and acceptability of the interventions.

CONDITIONS

Brief Title

Smoking Cessation Intervention Development for Homeless Youth

Who Can Participate

Age: 14Years - 24Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Youth who report having smoked some or every day in the past week
  • Youth aged 14 to 24 years
  • Youth who meet criteria for homelessness defined by the 2002 McKinney-Vento Act including those who lack a fixed, regular, and adequate nighttime residence; live in a welfare hotel, or place without regular sleeping accommodations; or live in a shared residence with other persons due to the loss of one's housing or economic hardship
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for eligibility assessment

Interview

Duration - Single session

Participants attend a semi-structured interview lasting about 60 minutes to help establish a theoretical model for smoking cessation tailored to homeless youth.

1 visit (in-person or remote)

Survey Completion

Duration - Single session

Participants complete a survey to further establish the theoretical model for smoking cessation tailored to homeless youth.

1 visit (can be remote or in-person)

Focus Groups

Duration - Short-term over a few weeks

Participants attend focus groups to identify and assess acceptability and feasibility of smoking cessation intervention components for homeless youth.

1 to 2 visits depending on group assignment

Outpatient Treatment

Duration - Duration as determined by intervention feasibility study

Participants take part in a feasibility study of smoking cessation intervention components coordinated with homeless youth services.

Visit frequency varies according to intervention schedule

Trial Site Locations

Total: 1 location

1

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States, 43210

Actively Recruiting

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Research Team

T

The Ohio State University Comprehensive Cancer Center

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

PREVENTION

Number of Arms

4

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