MedPath

Supporting Smoke-Free Policy Compliance in Public Housing

Not Applicable
Active, not recruiting
Conditions
Smoking Reduction
Smoking
Smoking Cessation
Smoking Behaviors
Interventions
Behavioral: Reduction (relocation and reduction of personal smoking) and cessation
Behavioral: Resident Endorsement
Registration Number
NCT05016505
Lead Sponsor
Columbia University
Brief Summary

This project seeks to determine the effectiveness of two types of interventions to reduce exposure to secondhand smoke in residential buildings. One intervention is geared toward all building residents (resident endorsement) and the other targets smokers (smoking reduction via relocation and reduction in personal smoking/cessation) with the goal of reducing personal smoking and secondhand smoke exposure.

Detailed Description

Smoke-free housing policies in multi-unit housing are promising and increasingly widespread interventions to reduce smoking and secondhand smoke exposure. Little research has identified factors that improve compliance with smoke-free housing policies in low-income multi-unit housing and test corresponding solutions.

The proposed randomized controlled trial (RCT) addresses key gaps in knowledge and capitalizes on key scientific opportunities by: 1) leveraging the federal mandate to ban smoking in a public housing system of more than sufficient size to conduct an adequately powered RCT; 2) expanding our understanding of smoke-free policy compliance beyond policy implementation by testing two novel treatments: a) in-residence smoking cessation and b) resident endorsement, while 3) addressing population and location-specific tobacco-related disparities.

The investigators hypothesize that the relocation/cessation plus resident endorsement intervention will yield significantly larger reductions in personal smoking and secondhand smoke exposure, compared to standalone interventions and the standard approach.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
512
Inclusion Criteria
  • NYCHA buildings in Manhattan & the Bronx (stratified evenly by borough) with more than 50 units, not undergoing major renovations.

Building

Exclusion Criteria
  • Buildings in a borough that is not in Manhattan or the Bronx
  • Buildings smaller than 50 units
  • Buildings undergoing major renovations
  • Buildings that are or will be part of Rental Assistance Demonstration (RAD) or Permanent Affordability Commitment Together (PACT)
  • Buildings that are mixed finance
  • Buildings that are exclusively for elderly
  • Buildings that are privately managed
  • Buildings that have other research studies ongoing

Participant Inclusion Criteria:

  • Recruit NYCHA residents via door knocking and lobby intercepts until we reach our targeted number per group (4 smokers, 4 non-smokers in each building).
  • Residents will be screened for smoking status. Both smokers and non-smokers to be recruited but only one participant- smoker or a non-smoker- will be recruited per apartment.
  • Smoking will be defined as those that report using a cigarette or other combustible tobacco product (e.g., little cigar, cigarillo) at least 5 days in the past month. Non-smokers include never smokers and former smokers who had quit 12 months ago or earlier.
  • Additional eligibility criteria include individuals above 18 years old living in the building at least 5 days/week and 9 months/year, not planning on moving in the next 2 years.

Participant Exclusion Criteria:

  • Individuals with severe physical or mental medical conditions (i.e. cognitive disability) or other factors that could limit participation or ability to give informed consent in the study at baseline or during follow-ups.
  • Individuals who participated in the earlier focus groups.
  • Individuals who only smoke non-tobacco products (e.g., marijuana).

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Compliance through reduction (relocation and reduction of personal smoking) and cessationReduction (relocation and reduction of personal smoking) and cessationSmokers will be referred by the survey team to peer educators from a community-based organization trained to provide peer to peer health education including tobacco cessation support. The peer educator will coordinate smoking cessation support, including serving as a liaison between participant and research team, providing information regarding the smoke-free policy and opportunities for relocation, and connecting participant to access to tobacco replacement therapy and/or physician support if deemed appropriate.
Compliance through resident endorsementResident EndorsementBuildings assigned will be targeted for a series of 2 in-residence programs that involve community forums and the creative arts to garner resident endorsements of smoke-free living environments. Premised on resident engagement, this arm seeks to impact social and physical dimensions of the residential environment to achieve compliance. The sessions will: 1) inform residents of risks associated with smoking and secondhand smoke; 2) identify reasons to have a smoke-free home, 3) ask residents to sign a pledge on paper and/or virtually; 4) display smoke-free signage on doors and/or social media pages with an original hashtag (#Smokefree\[building address\]); and 5) refer residents to the Smoke-free NYCHA website for information on the policy and existing cessation resources.
Compliance through reduction/cessation plus resident endorsement (combined)Reduction (relocation and reduction of personal smoking) and cessationThe combined intervention will be carried out in the buildings assigned to this RCT arm, which will provide in-residence programs based on the resident endorsement treatment and the smoking relocation/cessation treatment. Both will occur simultaneously with one geared toward all building residents (resident endorsement) and the other targeting smokers (smoking relocation/cessation) with the goal of reducing both personal smoking and secondhand smoke exposure.
Compliance through reduction/cessation plus resident endorsement (combined)Resident EndorsementThe combined intervention will be carried out in the buildings assigned to this RCT arm, which will provide in-residence programs based on the resident endorsement treatment and the smoking relocation/cessation treatment. Both will occur simultaneously with one geared toward all building residents (resident endorsement) and the other targeting smokers (smoking relocation/cessation) with the goal of reducing both personal smoking and secondhand smoke exposure.
Primary Outcome Measures
NameTimeMethod
Change in number of cigarettes smoked per dayMeasured at baseline (in person interview), 3 months (phone interview) and 12 months (in person interview)

Self-reported average number of cigarettes smoked per day among smokers

Change in salivary cotinineAt baseline and at the 12-month follow-up

Salivary cotinine (saliva collected as passive drool) will be measured for 25% of the sample among smokers and non-smokers alike

Change in secondhand smoke exposureMeasured at baseline (in person interview), 3 months (phone interview) and 12 months (in person interview)

Self-reported secondhand smoking exposure (hours of secondhand smoke exposure in the building in the past 7 days); among smokers \& non-smokers

Secondary Outcome Measures
NameTimeMethod
Change in number of hours of secondhand smoke exposureNumber of hours observed someone smoking indoors within the past 7 days measured at baseline (in person interview), 3 months (phone interview) and 12 months (in person interview)

Counted number of hours of exposure

Change in number of quit attemptsMeasured at baseline (in person interview), 3 months (phone interview) and 12 months (in person interview)

Mean number of quitting attempts among smokers

Change in number of participants with secondhand smoke observationsEver observing someone smoking indoors within the past 7 days measured at baseline (in person interview), 3 months (phone interview) and 12 months (in person interview)

Binary; whether participant has observed someone smoking indoors in the building; among smokers \& non-smokers

Change in number of participants with successful quit attemptsMeasured at baseline (in person interview), 3 months (phone interview) and 12 months (in person interview)

Binary; whether smokers have successfully quit

Change in number of smokersAt each building visit at baseline and 12 months

Counted number of people observed smoking in common areas

Change in number of cigarette buttsAt each building visit at baseline and 12 months

Counted number of cigarette butts observed in common areas

Trial Locations

Locations (1)

Columbia University Irving Medical Center

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New York, New York, United States

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