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NCT06598397 · ClinicalTrials.gov registry record · Phase 4

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

A Phase 4 study of Smoking Cessation and Human Immunodeficiency Virus (HIV), sponsored by New York University.

Recruiting
Registry status
Phase 4
Development phase
500
Enrollment target
1
Study location

NCT06598397 is a Phase 4 study of Smoking Cessation and Human Immunodeficiency Virus (HIV) that is actively recruiting participants, run by New York University. The registered enrollment target is 500 participants, roughly in line with the 472-participant average among 188 other Smoking Cessation trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT06598397, a Phase 4 study of Smoking Cessation and Human Immunodeficiency Virus (HIV), is actively recruiting participants, sponsored by New York University.

RECRUITING
Registry status
Phase 4
Development phase
500 participants
Enrollment target
1
Study location

Study 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.

Interventions

  • BEHAVIORAL Motivational Interviewing (MI) Counseling
  • BEHAVIORAL Peer Mentoring
  • BEHAVIORAL Skills-based Text Messaging
  • DRUG Combination NRT

Study Locations (1)

New York

  • New York University School of Global Public Health - New York

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2024-10-18
Est. Completion 2028-06-30
Phase Phase 4

Sponsor

New York University

83 total trials

What the Registry Record Tells You About NCT06598397

The ClinicalTrials.gov registry entry for NCT06598397 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 472-participant average among 188 other Smoking Cessation trials with a reported enrollment target. The listed sponsor is New York University, which has 83 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Smoking Cessation appearing as the primary indexed condition, and to 4 interventions - of which Motivational Interviewing (MI) Counseling is the first listed.

NCT06598397 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT06598397 about?

NCT06598397 is a clinical study titled "Using Multiphase Optimization Strategy (MOST) to Optimize a Cost-effective, Sustainable and Scalable Smoking Cessation Package for Smokers in HIV Clinical Care". 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.

What is the current status of trial NCT06598397?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 500 participants. The study started on 2024-10-18. Estimated completion is 2028-06-30.

What conditions does trial NCT06598397 study?

This clinical trial studies the following conditions: Smoking Cessation, Human Immunodeficiency Virus (HIV).

What interventions are being tested in trial NCT06598397?

The interventions under investigation include: Motivational Interviewing (MI) Counseling (BEHAVIORAL), Peer Mentoring (BEHAVIORAL), Skills-based Text Messaging (BEHAVIORAL), Combination NRT (DRUG).

Who is sponsoring clinical trial NCT06598397?

This trial is sponsored by New York University, which has 83 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06598397 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.