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Using Multiphase Optimization Strategy (MOST) to Optimize a Cost-effective, Sustainable and Scalable Smoking Cessation Package for Smokers in HIV Clinical Care

Status: Recruiting
Location: See location...
Intervention Type: Behavioral, Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This study's long-term goal is to improve clinical outcomes among smokers living with HIV (SLWH) by providing smoking cessation interventions in HIV clinical care that will increase the chances of quitting smoking, limits costs and burden on staff and reach many smokers living with HIV.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Status as HIV+

• Age 18 or older

• Currently smokes ≥ 5 CPD, on average, in past month

• Positive for salivary cotinine

• Able to understand the nature of the study and the consenting process

• Is engaged in HIV clinical care

• Living in larger NYC metropolitan area currently and for the next 6-8 months

Locations
United States
New York
New York University School of Global Public Health
RECRUITING
New York
Contact Information
Primary
Jennifer Cantrell, DrPH, MPA
jennifer.cantrell@nyu.edu
212-998-5797
Time Frame
Start Date: 2024-10-18
Estimated Completion Date: 2028-06-30
Participants
Target number of participants: 500
Treatments
No_intervention: Condition 1
Participants will receive the Core Component.
Experimental: Condition 2
Participants will receive the Core Component and Combination-NRT intervention.
Experimental: Condition 3
Participants will receive the Core Component and Text Messaging intervention.
Experimental: Condition 4
Participants will receive the Core Component as well as the Combination-NRT and Text Messaging interventions.
Experimental: Condition 5
Participants will receive the Core Component and Peer Mentoring intervention.
Experimental: Condition 6
Participants will receive the Core Component as well as the Combination-NRT and Peer Mentoring interventions.
Experimental: Condition 7
Participants will receive the Core Component as well as the Text Messaging and Peer Mentoring interventions.
Experimental: Condition 8
Participants will receive the Core Component as well as the Combination-NRT, Text Messaging and Peer Mentoring interventions.
Experimental: Condition 9
Participants will receive the Core Component and Motivational Interviewing Counseling intervention.
Experimental: Condition 10
Participants will receive the Core Component as well as the Combination-NRT and Motivational Interview Counseling interventions.
Experimental: Condition 11
Participants will receive the Core Component as well as the Text Messaging and Motivational Interview Counseling interventions.
Experimental: Condition 12
Participants will receive the Core Component as well as the Combination-NRT, Text Messaging and Motivational Interview Counseling interventions.
Experimental: Condition 13
Participants will receive the Core Component as well as the Peer Mentoring and Motivational Interview Counseling interventions.
Experimental: Condition 14
Participants will receive the Core Component as well as the Combination-NRT, Peer Mentoring and Motivational Interview Counseling interventions.
Experimental: Condition 15
Participants will receive the Core Component as well as the Text Messaging, Peer Mentoring and Motivational Interview Counseling interventions.
Experimental: Condition 16
Participants will receive the Core Component as well as the Combination-NRT, Text Messaging, Peer Mentoring, and Motivational Interview Counseling interventions.
Related Therapeutic Areas
Sponsors
Leads: New York University
Collaborators: National Cancer Institute (NCI)

This content was sourced from clinicaltrials.gov