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Tobacco Assessment and Intervention With Low-Income Persons Living With HIV-AIDS (PLWHA) in Community-Based AIDS Service Organizations

Feasibility of Tobacco Assessment and Intervention With Low-Income Persons Living With HIV-AIDS (PLWHA) in Community-Based AIDS Service Organizations

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01482923
Enrollment
65
Registered
2011-12-01
Start date
2011-11-22
Completion date
2019-10-21
Last updated
2019-11-04

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

Conditions

AIDS, HIV, Tobacco Cessation

Keywords

Tobacco Use Assessment, smoke tobacco, quit smoking, tobacco cessation, HIV/AIDS, Community-Based Service Organizations, 11-173, Low-Income Persons Living with HIV/AIDS

Brief summary

A treatment session especially for PLWHA to help them discuss and take action about their smoking may be useful.

Interventions

BEHAVIORALTreatment as usual

Participants in the Treatment as Usual study arm will be provided with the following: 1) brief smoking cessation counseling as recommended in the Public Health Service treatment guidelines; 2) direct referral to the NY/NJ State Quitline; 3) a brochure that describes the Quitline services and provides contact information via telephone or internet; 4) a NY State brochure on HIV and smoking that identifies the specific risks of smoking for PLWHA; and 5) referral assistance to participants who present with untreated co-morbid conditions.

BEHAVIORALAIR (Aspirations, Inspiration, Respiration)

Participants in the Aspirations, Inspiration, and Respiration study arm will receive all of the components of Treatment as Usual along with these additional components: 1) a lung age test to determine the ability and functioning of their lungs; 2) a personal lung health report with their lung age, the CO level of their breath, and a summary of their respiratory symptom assessment; 3) a review of this personal lung health report with a study counselor, 4) motivational interviewing techniques guided by Self-Determination Theory concepts to explicitly elicit at least one life aspiration of the patient and encourage discussion of such aspirations using an autonomy-supportive approach.

Sponsors

Gay Men's Health Crisis
CollaboratorUNKNOWN
The City College of New York
CollaboratorOTHER
AIDS Center of Queens County
CollaboratorUNKNOWN
Bronx AIDS Services
CollaboratorUNKNOWN
North Jersey Community Research Initiative
CollaboratorOTHER
Memorial Sloan Kettering Cancer Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 18 years or older as per self-report; * English speaking; * New York or New Jersey State resident; * HIV-positive serostatus direct referral from a CAB agency staff member, which verifies that the person is an HIV+ client, or by as verified by presentation of medical evidence (i.e.,confirmatory test result, ARV prescription, M11Q form, or lab results); * Self-report of smoking \> or = to 20 cigarettes (\> or = to one pack) within the prior 7 days; * To confirm smoking status, the carbon monoxide alveolar breath test must be \> or = to 10 ppm; * To confirm cognitive functioning, score on the in-person BLESSED Exam must be \< or = to 10; * Low income, defined by either: 1) Proof of Medicaid insurance, or 2) Self-report of income at 50% or below median income for New York State for New York State residents, or if a New Jersey resident, at or below 50% median income for New Jersey

Exclusion criteria

* Presence of current severe psychopathology that would limit study participation (e.g., unstable schizophrenia, bipolar disorder recent changes to medication noncompliance); * Currently receiving smoking cessation treatment elsewhere.

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of a motivational tobacco cessation intervention2 yearsThe study will test whether the percentage of eligible and enrolled study participants who complete the assigned intervention is significantly different from a population of percentages centered at 45%, i.e., the null population percentage, considered a percentage too low to be compatible with feasibility.

Secondary

MeasureTime frameDescription
Estimate the differences between the experimental intervention2 yearsAssess potential factors influencing study participation by community organizations and, as the description, Descriptive statistics will be summarized by participating community organizations on each organization's Implementation Factors assessment, an agency study participation measure developed for this project. The measure assesses how many clients the agency has referred, what means were used to recruit, and what barriers to recruitment were encountered, and an open-ended question is provided for additional input.

Countries

United States

Outcome results

None listed

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