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Tobacco Cessation Tailored to Patients Living With HIV (PLWH) in Brazil

Not Applicable
Completed
Conditions
HIV Infections
Tobacco Use Cessation
Interventions
Behavioral: Tobacco cessation
Registration Number
NCT05560243
Lead Sponsor
University of Alabama at Birmingham
Brief Summary

The overall goal of this feasibility study is to make adaptations to these evidence-based approaches in collaboration with PLWH and health care providers working with this population, and develop, implement, and evaluate the feasibility and scalability of a theory-based, culturally relevant tobacco cessation intervention for PLWH receiving care through the public health system in a southern town in Brazil (Londrina). This proposal will focus on the intervention development, pretesting, and feasibility testing. The primary outcome will be a 7-day point prevalence abstinence (defined as no tobacco use in the past 7 days and verified through measurement of salivary cotinine and exhaled carbon monoxide levels) at 6-month follow-up. We will also conduct detailed treatment fidelity and scalability assessments (acceptability, feasibility, potential reach and adoption, alignment with the strategic context) to inform a full-scale efficacy trial.

Detailed Description

This study aims at developing and examining feasibility and scalability of a theory-based, culturally relevant tobacco cessation intervention for PLWH receiving care through the public health system in a southern town in Brazil. It consists of three phases: formative assessments with patients and health care providers to inform relevant components of the intervention, pretesting of the intervention components, and pilot testing of the intervention (feasibility).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
56
Inclusion Criteria
  • PLWH (that is, patients with a confirmed HIV diagnosis) receiving care at the reference center in Londrina
  • 18 years of age and older; (c) smoke at least 5 cigarettes (industrialized or hand-rolled) per day Smoked within the past seven days.
  • No intent to move from the area served by reference center in Londrina within the next 12 months.
Exclusion Criteria
  • History of hypertension
  • History of angina
  • History of asthma
  • On medication for depression.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
InterventionTobacco cessationPatients will receive a tobacco cessation intervention
Primary Outcome Measures
NameTimeMethod
Number of Participants With a 7-day Prevalence Abstinence of Tobacco Use6-month follow-up

7-day point prevalence abstinence (defined as no tobacco use in the past 7 days and verified through measurement of salivary cotinine and exhaled carbon monoxide (CO) levels) at 6-month follow-up.

Secondary Outcome Measures
NameTimeMethod
Participants With Tobacco Use Abstinence Based on Salivary Cotinine at 7-month Follow-up.7 months

Tobacco use abstinence based on salivary cotinine was assessed at 7-month follow-up

Trial Locations

Locations (1)

Universidade Estadual de Londrina

🇧🇷

Londrina, Paraná, Brazil

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