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Development and Pilot Testing of the Sense2Quit App

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Columbia University

Status

Completed

Conditions

HIV Infections
Smoking Cessation

Treatments

Behavioral: Sense2Quit App

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05609032
AAAT7031
1R21CA265961-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This is a pilot randomized controlled trial to examine the feasibility, acceptability and preliminary efficacy of the Sense2Quit App in a sample of 60 PLWH who smoke.

Full description

The estimated 40-70% of persons living with HIV (PLWH) who smoke cigarettes experience substantial tobacco-related morbidity and mortality. For PLWH, apart from achieving and maintaining a suppressed viral load, tobacco cessation is the most important health behavior they can undertake to maximize both quality of life and life expectancy. However, the currently available evidence for improving tobacco cessation among PLWH is inadequate. Few tobacco cessation interventions have been tested among PLWH, and of those which have, there is 'very low' quality evidence that they were effective in the short-term and 'moderate' quality evidence indicating similar outcomes to controls in the long-term. Thus, it is critical to develop evidence-based tobacco cessation interventions to address the complex and unique needs of PLWH. In response to this need, the investigators propose to develop a mobile intervention for PLWH who smoke building on Sense2Quit, a multi-component intervention that links a smartphone app to a smartwatch to provide real-time quit reminders to curtail relapses and avoid potential trigger. This real-time feedback is critical especially in the first few weeks of a quit attempt.

The proposed Sense2Quit intervention for PLWH who smoke cigarettes is a novel and evidence-driven intervention using mobile technology to improve tobacco cessation. This will be the first study to develop and pilot test an innovative tobacco cessation intervention for PLWH. The final product of this study will be the basis for an R01 application to conduct a large-scale efficacy study for this population.

The investigators are confident that the proposed intervention will be a high impact intervention for improving tobacco cessation among PLWH and have long-term implications for overall improvement in the public's health.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • PLWH confirmed through medical records or pill bottles for antiretroviral therapy (ART)medications.
  • ≥ 18 years of age;
  • Own an Android smartphone;
  • Understand and read English;
  • Not pregnant or breastfeeding (due to contraindications for Nicotine Replacement Therapy [NRT]);
  • Permanent contact information;
  • Smokes ≥5 cigarettes per day for the past 30 days;
  • Interested in quitting smoking within 30 days;
  • Blows ≥5 ppm eCO into a breath analyzer at baseline.

Exclusion criteria

  • Use of tobacco products other than cigarettes (i.e. cigars, piped tobacco, chew, snuff)
  • Planning to move within 3 months of enrollment;
  • Positive history of a medical condition that precludes nicotine patch use;
  • Current use of NRT or other smoking cessation medications (e.g., Chantix or Zyban);
  • Current enrollment in another smoking cessation program.
  • Alcohol dependence measured through the AUDIT-C
  • A household member is also participating in the Sense2Quit study (due to study contamination).

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

Intervention (App Arm)
Experimental group
Description:
Participants randomized to the intervention arm will receive access to the Sense2Quit App (A multi-component intervention that links a smartphone app to a smartwatch to provide real-time quit reminders to curtail relapses and avoid potential triggers), standard smoking cessation counseling, and nicotine replacement therapy.
Treatment:
Behavioral: Sense2Quit App
Control
No Intervention group
Description:
Participants randomized to the control arm will receive standard smoking cessation counseling and referral to quitline.

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Rebecca Schnall, PhD, MPH; Maeve Brin

Data sourced from clinicaltrials.gov

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