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Intervention Study to Increase Smoking Cessation Rates Among Public Housing Residents

Health Advocates as a Vehicle to Improve Treatment for Smokers in Public Housing

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01651611
Enrollment
330
Registered
2012-07-27
Start date
2011-09-30
Completion date
2014-09-30
Last updated
2016-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Cessation

Keywords

Tobacco Cessation, Public Housing, Community Health Workers, Motivational Interviewing, Patient centered, Low-income, Tobacco Treatment Advocates, Social Epidemiology, Smoking cessation predictors, Behavioral Intervention, Non-pharmacologic

Brief summary

The purpose of this study is to determine whether public housing residents trained in Tobacco Cessation and Motivational Interviewing Techniques to become Tobacco Treatment Advocates(TTA) will be effective in increasing the quit rate of smokers in Boston Public Housing. The investigators hypothesize that smokers that receive multiple TTA visits will be more likely to (1) use smoking cessation resources and (2) quit compared to smokers who receive a single visit.

Detailed description

The study is a group-randomized trial in which 10 pubic housing developments (PHDs) are randomized to the experimental condition and 10 to the control condition. All smokers who enroll in the study at a particular PHD receive the same intervention. Smokers at control sites receive written materials that offer strategies for quitting and information about availability of treatment programs, as well as a one-time meeting with a Tobacco Treatment Advocate (TTA). The intervention group receives the same written materials but also has much more extensive interactions with a TTA. TTAs provide peer counseling (Peer Counseling is defined as: performance of limited counselor functions, under counselor supervision, by person of similar age,gender, race, ethnicity and/or SES of the counselee) to smokers during in- person Motivational Enhancement meetings (target range 7-9) as well as additional in person and phone contacts, as needed for each participant, over a 6-month period. TTAs receive intensive training in motivational interviewing and smoking cessation counseling deliver the intervention components (counseling activities and provision of environmental supports) in addition to encouraging utilization of smoking cessation treatment programs such as the Smokers' QuitLine (SQL) and clinic-based programs. In order to avoid the potential for contamination due to TTAs interacting with participants at both intervention and control sites, meetings with participants at control sites are conducted by special Control TTAs. Data are collected from study participants at baseline, 3 months, 7 months and 12 months, and also from the SQL and clinics.

Interventions

BEHAVIORALMotivational interviewing

The TTA will use motivational interviewing (MI) techniques to assess the participant's motivation and readiness to quit, suggest plans, and assist the participant in selecting a method of treatment.

BEHAVIORALSmoking cessation counseling

The TTA will provide information to the participant regarding evidence-based treatments for smoking cessation, including counseling and nicotine replacement therapy (NRT); assist in a quit plan; and discuss issues such as obtaining social support, staying in treatment, and dealing with lapses.

BEHAVIORALNavigation to smoking cessation resources

The TTA will assist participants in obtaining NRT and getting connected to smoking cessation counseling services, such as the Smokers' Quitline and clinic-based programs.

BEHAVIORALSocial support

Meetings with the TTA will be a source of social support for the participant as they attempt to quit or stay quit.

Sponsors

Harvard School of Public Health (HSPH)
CollaboratorOTHER
The Miriam Hospital
CollaboratorOTHER
Boston Housing Authority
CollaboratorUNKNOWN
Boston University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

* Current smoker, defined as having smoked in last 100days * Housing Sites: Sites are eligible for the study if they have 50+ smokers determined by synthetic estimates based on citywide survey data. * Age 18-79 * Current everyday or someday smokers * Planning to quit smoking in 30 days or thinking about quitting in next 6 months, * Have smoked 100 cigarettes in lifetime * Speak English or Spanish * Plan to live in Public Housing for next 12 months * Able and willing to provide consent

Exclusion criteria

* Smokers less than 18 years of age at time of consent. * Unable to communicate orally in English or Spanish. * Currently using pharmacological treatment for smoking cessation * Currently working with the Smokers Quitline or other Community Health Center based cessation program * Cognitive/ psychiatric conditions that would interfere with ability to understand and participate in the study * Have been abstinent for 7 or more days.

Design outcomes

Primary

MeasureTime frameDescription
Point prevalence smoking abstinence7 months7 and 30-day abstinence from smoking by self-report with verification by carbon monoxide breath test

Secondary

MeasureTime frameDescription
Utilization of smoking cessation resources7 monthsUse of SQL, smoking cessation programs at health clinics or hospitals, physician counseling

Other

MeasureTime frameDescription
Medication use3 months, 7 months, 12 monthsUse of nicotine replacement therapy and/or other smoking cessation medications

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026