Project CASA in Promoting Smoke-Free Indoor Air Policy in Mexican American Households

NCT ID: NCT00850954

Last Updated: 2023-09-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

168 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-08-08

Study Completion Date

2018-08-07

Brief Summary

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This trial studies the effect of an intervention program, Project CASA, on smoking cessation and reducing secondhand smoke exposure in Mexican American households. Project CASA, comprising pamphlets and fotonovelas (illustrated storybooks), may provide valuable information to participants on how to improve the air quality in their homes.

Detailed Description

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PRIMARY OBJECTIVES:

I. Reduction in secondhand smoke exposure: The study will distinguish if a tailored intervention designed to address the needs of the target group will reduce objectively and subjectively measured secondhand smoke exposure of nonsmokers in Mexican American (MA) households.

Ia. Develop tailored fotonovelas for intervention implementation. II. Smoking cessation: The study will identify if a tailored intervention designed to address the needs of the target group will help the primary smokers in the household quit smoking.

III. Stages of change: The study will identify if the proposed intervention will have a significant impact on the primary smoker(s) progression through the stages of smoking cessation.

IV. Knowledge and attitudes: The study will identify if the proposed intervention will result in better knowledge and changed attitudes towards secondhand smoke exposure among members of MA households (smokers and nonsmokers) compared to standard care.

V. Perceived health: The study will distinguish whether reduced exposure to secondhand smoke would improve perceived health.

OUTLINE: Participants are assigned to 1 of 2 groups based on smoking status.

GROUP I (SMOKERS): Participants receive smoking cessation intervention materials based on transtheoretical model of change (TTM).

GROUP II (NON-SMOKERS): Participants receive fotonovelas and other materials on secondhand smoking and how to assist the smoker in quitting.

Participants are followed up at 6 and 12 months to assess for home air quality.

Conditions

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Cigarette Smoker Current Smoker Currently Living With Smoker

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Group I (smoking cessation)

Participants receive smoking cessation intervention materials based on TTM.

Group Type EXPERIMENTAL

Smoking Cessation Intervention

Intervention Type BEHAVIORAL

Receive smoking cessation materials based on TTM

Survey Administration

Intervention Type OTHER

Ancillary studies

Group II (informational)

Participants receive fotonovelas and other materials on secondhand smoking and how to assist the smoker in quitting.

Group Type EXPERIMENTAL

Informational Intervention

Intervention Type OTHER

Receive information on secondhand smoke and supporting smoker in quitting

Survey Administration

Intervention Type OTHER

Ancillary studies

Interventions

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Informational Intervention

Receive information on secondhand smoke and supporting smoker in quitting

Intervention Type OTHER

Smoking Cessation Intervention

Receive smoking cessation materials based on TTM

Intervention Type BEHAVIORAL

Survey Administration

Ancillary studies

Intervention Type OTHER

Other Intervention Names

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Smoking and Tobacco Use Cessation Interventions

Eligibility Criteria

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Inclusion Criteria

* Live in the targeted Mexican American neighborhoods.
* Can read Fotonovelas in English and Spanish.
* Access to telephone.
* Smoker in household (adult \[18+\] person living in the household who smokes INSIDE at least one cigarette a week).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

M.D. Anderson Cancer Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Alexander V Prokhorov

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

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M D Anderson Cancer Center

Houston, Texas, United States

Site Status

Countries

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United States

Related Links

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http://www.mdanderson.org

University of Texas MD Anderson Cancer Center Website

Other Identifiers

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NCI-2019-02502

Identifier Type: REGISTRY

Identifier Source: secondary_id

2006-0440

Identifier Type: OTHER

Identifier Source: secondary_id

P30CA016672

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2006-0440

Identifier Type: -

Identifier Source: org_study_id

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