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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02506829
Other study ID # 72426
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2015
Est. completion date May 20, 2019

Study information

Verified date December 2020
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators plan to compare the impact of two approaches for smoking cessation on smoking abstinence, use of evidenced-based therapy, and quality of life among a diverse population of patients at the Manhattan campus of the VA New York Harbor Healthcare System, which serves a critical safety-net role for urban veterans. During hospitalization, all smokers will receive usual care. Patients will be randomized to one of two arms: financial incentives plus usual care vs. usual care alone, which includes referral to the state Quitline. All patients enrolled in the study will be offered nicotine replacement therapy. The investigators will conduct follow-up assessments at 2 weeks, 2 months, 6 months and 12 months after discharge. The primary study outcome is smoking abstinence at 6-month follow-up, verified by salivary/urinary cotinine.


Recruitment information / eligibility

Status Completed
Enrollment 182
Est. completion date May 20, 2019
Est. primary completion date March 5, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. age = 18 years, 2. smoked tobacco during the prior 30 days, 3. have an active U.S. phone number and address, 4. can provide consent in English and 5. are in at least the contemplative stage of change for quitting smoking, as assessed by a single measure, readiness to quit Exclusion Criteria: 1. use only smokeless tobacco, 2. are pregnant or breastfeeding, 3. are discharged to an institution (e.g., nursing home, long-term care facility), 4. are unable to provide informed consent, or do not have cognitive ability to enroll or participate in the study

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Smoking cessation counseling (Quitline)

Smoking cessation pharmacotherapy (e.g, nicotine replacement therapy)

Financial incentives


Locations

Country Name City State
United States New York University School of Medicine New York New York

Sponsors (3)

Lead Sponsor Collaborator
NYU Langone Health Robert Wood Johnson Foundation, University of California, Los Angeles

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Smoking abstinence assessed by self-reported and biochemically verified by salivary cotinine Assessed by self-report questionnaire, and biochemically verified by salivary cotinine 6 months
Secondary Smoking abstinence assessed by self-report Assessed by self-report questionnaire 6 months
Secondary Use of evidence based treatment (e.g. counseling and smoking cessation medications) assessed by discharge prescriptions, Quitline records, receipts, letters and/or self-report Assessed by discharge prescriptions, Quitline records, receipts, letters and/or self-report 2 weeks and 2 months
Secondary Quality of life as measured by the EQ5-D and VR-12 As measured by the EQ5-D and VR-12 6 months
Secondary Short term return on investment of using financial incentives to promote smoking cessation (Cost analysis) Cost analysis involving hospital utilization data, electronic health records and patient-reported healthcare utilization 12 months
Secondary Long term return on investment of using financial incentives to promote smoking cessation (Cost analysis) Cost analysis involving hospital utilization data, electronic health records and patient-reported healthcare utilization 3 years
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