Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID05738408

Remote Smoking Cessation Support for Patients Hospitalized with Heart Problems Combining Financial Incentives and Nicotine Replacement Therapy To Improve Quitting After Hospital Discharge

Led by University of Vermont Medical Center · Updated on 2025-01-20

50

Participants Needed

1

Research Sites

172 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating new strategies to help patients hospitalized for acute coronary events, such as myocardial infarction or coronary revascularization, to quit smoking. This study focuses on whether combining financial incentives with medications to reduce withdrawal symptoms can improve smoking cessation rates in cardiac patients, a group with high smoking rates and significant health risks from continued smoking. The goal is to enhance adherence to smoking cessation guidelines and improve cardiac recovery outcomes. Participants in the intervention group will receive a combination of nicotine replacement therapy (NRT) and a 12-week program of financial incentives for biochemically verified smoking abstinence. Treatment begins during hospitalization and continues remotely after discharge to bridge the care gap when relapse risk is high. The financial incentives are administered by clinic staff, and NRT includes both short- and long-acting forms to maximize effectiveness. During the study, participants will be monitored for smoking status verified biochemically at 3 months. Researchers will assess adherence to smoking cessation, engagement with treatment, and cardiac recovery outcomes. Participants will be supported through the critical period following hospital discharge when smoking relapse is most common, with continued follow-up to measure the impact of the combined behavioral and pharmacologic intervention.

CONDITIONS

Official Title

Remote Smoking Cessation in Hospitalized Cardiac Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Hospitalized for an acute coronary event including myocardial infarction or coronary revascularization (percutaneous intervention or coronary artery bypass)
  • Live within 30 miles of the University of Vermont Medical Center
  • Aged 18 years or older
  • Current cigarette smoker, defined as any cigarette use in the week before hospital admission and averaging more than 5 cigarettes per day over the past 3 months
Not Eligible

You will not qualify if you...

  • Severe dementia or Alzheimer's disease
  • Active cancer, excluding non-melanoma skin cancer or low-grade prostate cancer under active surveillance
  • Exercise-limiting vascular or neuromuscular disease
  • Non-English speaking
  • No reliable smartphone access
  • Current regular use of smokeless tobacco or other non-combusted tobacco products

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Vermont Medical Center

Burlington, Vermont, United States, 05405

Actively Recruiting

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Research Team

S

Sherrie Khadanga, MD

D

Diann Gaalema, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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