Recruiting

Smoke-Free Home Intervention

Sponsor:

Emory University

Code:

NCT06583148

Conditions

Tobacco-Related Carcinoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Best Practice

Smoking Cessation Intervention

Survey Administration

Study Details

Brief summary:

This clinical trial evaluates a smoke-free home intervention for reducing exposure to secondhand smoke from commercial tobacco in homes of participants who live in rural tribal communities. Smoke-free homes are an innovative and relatively untapped strategy for cancer prevention in rural tribal communities. Smoke-free policies, including those that target homes, can reduce exposure to secondhand smoke and support smoking cessation. Rural and racial/ethnic inequities intersect to increase tobacco-related harms among Indigenous populations. A smoke-free home program may improve the health of the household as well as impact smoking behavior among the family unit by reducing secondhand smoke exposure.

Conditions

Tobacco-Related Carcinoma

Study ID

NCT06583148

Start date

Nov 15, 2024

Status verified date

Dec, 2025

Completion date

Jan 31, 2029

Anticipated

Primary completion date

Jan 31, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • 18 years of age and older
  • Self-report as being a smoker or living with a smoker
  • Indicate that they do not reside in a smoke-free home
  • Identify as living in an American Indian household

Exclusion Criteria:

  • Children under the age of 18 will not be included

Study Design

Enrollment

575 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

experimental: Group I (smoke-free home program)

Participants receive the smoke-free home program, consisting of mailed educational information about smoke-free homes at enrollment and in weeks 4 and 6, and attend one coaching call in week 2.

active comparator: Group II (waitlist control)

Participants receive usual care on study. Participants may optionally receive the smoke-free home program following the 6 months follow-up.

Interventions

Best Practice

Receive usual care

Smoking Cessation Intervention

Receive the smoke-free home program

Survey Administration

Ancillary studies

Primary outcome measure

  • Self-Reported Smoke-Free Home [ Time Frame: At 3 and 6 months ]

Central Contacts and Locations

Central contacts

Locations

Emory University Hospital/Winship Cancer Institute

Recruiting

Atlanta, Georgia, United States, 30322

Contacts

Michelle Kegler, DrPH, MPH

404-712-9957mkegler@emory.edu

Principal Investigator:

Michelle Kegler, DrPH, MPH

More Information

Sponsor

Emory University

Last update posted

Dec 8, 2025

Last verified

Dec, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Emory University on 2025-12-08.