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Recruiting NCT06583148

A Smoke-Free Home Intervention in Tribal Communities

No phase Interventional Tobacco-Related Carcinoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Best Practice, Smoking Cessation Intervention, Survey Administration.
Who it may be relevant to
Registry conditions: Tobacco-Related Carcinoma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Assessing the Effectiveness of a Smoke-Free Home Program in Tribal Communities

Overview

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.

Detailed description

PRIMARY OBJECTIVE:

I. To assess the effectiveness of a smoke-free homes intervention for tribal communities.

OUTLINE: Participants are randomized to 1 of 2 groups.

GROUP I: 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.

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

After completion of study intervention, participants are followed up at 3 and 6 months.

Interventions

  • Other Best Practice
    Receive usual care
  • Behavioral Smoking Cessation Intervention
    Receive the smoke-free home program
  • Other Survey Administration
    Ancillary studies

Primary outcome measures

  • Self-Reported Smoke-Free Home [Time frame: At 3 and 6 months]
Secondary outcome measures (4)
  • Smoke-Free Vehicles Assessed Via Telephone Interview [Time frame: At 3 and 6 months]
  • Secondhand Smoke (SHS) Exposure In The Home Assessed via Telephone Interview [Time frame: At 3 and 6 months]
  • Number of Cigarettes Smoked In the Home [Time frame: At 3 and 6 months]
  • Public Support for Smoke-Free Tribal Housing Assessed Via Telephone Interview [Time frame: At 3 and 6 months]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Prevention

Study locations

United States · 1 center
  • Emory University Hospital/Winship Cancer Institute — Atlanta

Identifiers

NCT: NCT06583148 · STUDY00006459 · NCI-2024-06174 · STUDY00006459 · RSPH6261-24 · P30CA138292 · R01CA268024

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗