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Clinical Trial Summary

PASS2 aims to expand upon the recently completed study (PASS intervention), which tested the telephone delivery of a cognitive behavioral intervention (CBI). This study will use Interactive Voice Response (IVR) to optimize the intervention's effectiveness for smoking cessation among Veteran smokers with chronic pain.


Clinical Trial Description

Veterans with chronic pain represent an important population in which to focus smoking cessation efforts. Smoking cessation among patients with chronic medical illnesses substantially decreases morbidity and mortality; yet, many patients (>50%) with chronic pain continue to smoke. This study aims to: 1. Determine whether the existing integrated pain and smoking cessation (PASS intervention) augmented with IVR (PASS-IVR) is superior to treatment as usual (e.g., referral to standard VA smoking cessation clinic) enhanced with pharmacotherapy tele-consult (E-TAU) at 6 (primary endpoint) and 12 months on cigarette abstinence rates among non-depressed Veterans with chronic pain. 2. Determine whether PASS-IVR is superior to E-TAU at 6 (primary endpoint) and 12 months on pain interference. 3. Examine critical components of the intervention process to inform future program implementation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06442514
Study type Interventional
Source VA Office of Research and Development
Contact Lori A Bastian, MD MPH
Phone (203) 932-5711
Email Lori.Bastian@va.gov
Status Not yet recruiting
Phase N/A
Start date December 1, 2024
Completion date May 31, 2028

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