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NCT Number: NCT05786547

V+PSF-M for Tobacco Cessation in HIV Care in India

The goal of this research study is to test an intervention to help quit tobacco use in participants with Human Immunodeficiency Virus (HIV).

The study interventions used in this research study are:

* Positively Smoke Free - Mobile (PSF-M) (mobile behavioral program) * Varenicline (or Chantix, apovarenicline, Champix or Nocrav)

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Key information

About this study

Open-label, practice-based randomized trial of varenicline + Positively Smoke Free-Mobile (PSF-M) for people living with Human Immunodeficiency Virus (PWH) who smoke or use both smoked and smokeless tobacco compared with a group that receives standard care including brief advice and quitline referral.

Positively Smoke Free (PSF) is a behavioral intervention which has been tested in multiple formats including a mobile version. Varenicline is the single most-effective pharmacotherapy agent for quitting tobacco with demonstrated efficacy for cessation of cigarettes, smokeless tobacco, and cessation among smokers with comorbidities

In this study, participants will be randomized to either Group 1: Varenicline + Positively Smoke Free-Mobile adapted for Chennai versus Group 2: Standard care with brief tobacco cessation advice and referral to the national quitline.

Research procedures include screening for eligibility, in-clinic visits, and completion of surveys and questionnaires.

Participation in this study is expected to last about 24 weeks.

It is expected about 400 people will take part in this research study.

This study is funded by the National Cancer Institute of the National Institute of Health (NIH).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (≥18 years)
  • Confirmed HIV diagnosis
  • Self-reported current smoking or dual tobacco use verified either by exhaled carbon monoxide ≥7 ppm, or by positive qualitative cotinine point-of-care test
  • Able to read at 6th grade level or greater and speak Tamil, Telugu or English
  • Able to use varenicline safely based on evaluation by primary provider at VHS
  • Women of childbearing potential who consent to use a medically approved method of contraception or abstain from intercourse while taking study medication and for one month after.
  • Ready to quit or interested in quitting

Exclusion criteria

  • Pregnant or planning to become pregnant in the next 6 months
  • Breastfeeding
  • Myocardial infarction in past 30 days or unstable angina
  • History of liver or kidney failure
  • Alanine aminotransferase and Aspartate aminotransferase > 2 times upper limit of normal or creatinine clearance <50 in past 6 months
  • History of suicide attempt
  • Current suicidal ideation
  • Untreated or unstable major depressive disorder
  • History of psychosis or on anti-psychotic medications
  • Cognitive impairment limiting ability to consent
  • Allergy to varenicline

Treatment and study plan

Varenicline

Drug

Per package dosing, tablet taken orally

Other names: Champix, apovarenicline, Nocrav

Positively Smoke Free Mobile (PSF-M)

Behavioral

Behavioral tobacco cessation intervention for people living with HIV, delivered via mobile phone

Standard Care

Behavioral

Brief cessation advice plus referral to local tobacco quitline

Primary outcomes

  1. 7-Day Point Prevalent Abstinence Rate

    Time frame: 24 weeks post-randomization

    Defined as abstinence from all combustible and smokeless tobacco products in the 7 days preceding 24-week follow-up supported by a negative urine cotinine test of < 50 ng/ml

Secondary outcomes

  1. 7-day self-reported Point Prevalent Abstinence Rate

    Time frame: 4 weeks post-randomization

    Defined as abstinence from all combustible and smokeless tobacco products in the 7 days preceding follow-up

  2. 7-day self-reported Point Prevalent Abstinence Rate

    Time frame: 12 weeks post-randomization

    Defined as abstinence from all combustible and smokeless tobacco products in the 7 days preceding 24-week follow-up supported by a negative urine cotinine test of < 50 ng/ml

Study contacts

Contact information is provided by the study sponsor or research team.

Gina Kruse, MD

CONTACT

[email protected]

303-724-4811

Yamila L Sierra, MPH

CONTACT

[email protected]

(303) 724-4549

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Varenicline and Mobile Behavioral Assistance for Tobacco Cessation in HIV Care in India

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Mar 27, 2023
Registry last updated
Jun 15, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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