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Clinical Trial Summary

This study conduct a two-arm, parallel-group randomized controlled trial. The study will recruit and randomize 900 smokers (n=450 per arm) to either: (1) Control: Standard Smoking Cessation Counseling or (2) Intervention: Integrated Financial-Smoking Cessation Counseling.


Clinical Trial Description

The study is a two-arm, parallel-group RCT. The study will recruit and randomize 900 low-income smokers (n=450 per arm) to either: (1) Control: Standard Smoking Cessation Counseling or (2) Intervention: Integrated Financial-Smoking Cessation Counseling. Both groups will receive 8 weeks of nicotine replacement therapy. The study will survey participants at baseline, 6 months, and 12 months to assess outcomes and mechanisms, and biochemically verify self-reported abstinence at 12 months (our primary outcome). The study will assess and compare the costs and cost-per-quit in the two treatment arms. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05154669
Study type Interventional
Source NYU Langone Health
Contact Erin Rogers, DrPH
Phone 646-501-2544
Email erin.rogers@nyulangone.org
Status Recruiting
Phase Phase 3
Start date December 8, 2022
Completion date October 1, 2027

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