Varenicline
DrugPer package dosing, tablet taken orally
Other names: Champix, apovarenicline, Nocrav
NCT Number: NCT05786547
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)
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 3
VHS Infectious Disease Medical Centre, CART Clinical Research Site, Chennai, Tamil Nadu, India
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).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Per package dosing, tablet taken orally
Other names: Champix, apovarenicline, Nocrav
Behavioral tobacco cessation intervention for people living with HIV, delivered via mobile phone
Brief cessation advice plus referral to local tobacco quitline
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
Time frame: 4 weeks post-randomization
Defined as abstinence from all combustible and smokeless tobacco products in the 7 days preceding follow-up
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
Contact information is provided by the study sponsor or research team.
Gina Kruse, MD
CONTACT
Yamila L Sierra, MPH
CONTACT
University of Colorado, Denver
Other
Varenicline and Mobile Behavioral Assistance for Tobacco Cessation in HIV Care in India
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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