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Clinical Trials/NCT02513069
NCT02513069
Completed
Not Applicable

Mobile Contingency Management for Smoking Cessation in Returning US Veterans

Duke University1 site in 1 country291 target enrollmentJanuary 2015
ConditionsSmokingVeterans

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Smoking
Sponsor
Duke University
Enrollment
291
Locations
1
Primary Endpoint
smoking, self-report
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The primary goal of the study is to evaluate the effectiveness of a combined tele-health and contingency management (CM) intervention that the investigators call mobile CM, or mCM, in promoting smoking abstinence in US Veterans. The mCM intervention will combine a mobile system to reward non-smoking, smoking cessation counseling, and smoking cessation medications. The primary aim is to evaluate how effective this intervention is in promoting smoking abstinence compared to telehealth interventions for smoking cessation.

Detailed Description

Despite recent efforts to expand reach of smoking cessation treatment options beyond clinic based care, smoking cessation treatment including the use of smoking cessation aids remain greatly underutilized. If cessation programs are to have significant impact (Impact = Reach X Efficacy) on changing health behavior at the population level, there is a fundamental need to develop new and innovative strategies to increase treatment intensity, access, and participation. The use of intensive behavioral therapies, such as contingency management (CM), have demonstrated efficacy for reducing smoking in difficult-to-treat populations, but have had limited reach given the need to verify abstinence multiple times daily via clinic based monitoring. The development of a mobile health (mHealth) platform to provide CM has made the use of intensive CM approaches portable and feasible. The primary goal of the current study is to evaluate the effectiveness of a proactive tele-health intervention that combines evidenced based treatment for smoking cessation with smartphone based, portable contingency management on smoking rates. The central hypothesis is that increasing the intensity of available tele-health smoking approaches through the addition of mobile CM will be an effective way to reduce smoking rates in Veterans returning from the Iraq/Afghanistan wars. Guided by strong preliminary data, this hypothesis will be tested in a comparative effectiveness trial with a two-group design in which 260 Veteran smokers will be randomized to receive either an "mCM" intervention which combines evidence-based cognitive-behavioral telephone counseling (TC), a tele-medicine clinic for access to nicotine replacement (NRT), and mCM administered through a smart phone or to a control condition that will provide controls for therapist, medication, time and attention effects. Specific aims are to evaluate (1) the impact of mCM on rates of abstinence from cigarettes as measured by bio-verified, self-reported prolonged abstinence at 3-month, 6-month, and 12 month post-randomization follow-up, (2) the relative cost-effectiveness of the mCM intervention in quality adjusted life years (QALY), and (3) potential treatment mediators including self-efficacy and treatment process mechanisms. The approach is innovative because it builds upon advances in mHealth technology and will be the first evaluation of smart phone based mobile CM in conjunction with other evidence-based smoking cessation treatment for OEF/OIF/OND Veterans. There is a surprising lack of research aimed at evaluating multi-component smoking cessation interventions that integrate CM with evidence-based cognitive-behavioral treatment and smoking cessation aids such as NRT. Cigarette smoking remains the most lethal substance use disorder in the United States and military veterans are at particular high risk for smoking related morbidity and mortality. The significance of identifying cost-effective approaches to decreasing tobacco use in the relatively young and at-risk cohort of returning Veterans could be tremendous as it will prevent significant morbidity and mortality.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
February 14, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Smoked at least 10 cigarettes on at least 15 of 30 days before screening
  • Served during OEF/OIF/OND era
  • Are willing to make a smoking cessation attempt
  • Enrolled in the Durham VA for ongoing care
  • English speaking

Exclusion Criteria

  • Use and unwillingness to stop use of other forms of nicotine such as cigars, pipes, or chewing tobacco
  • Active diagnosis of a primary psychotic disorder per medical record
  • Are currently imprisoned or in psychiatric hospitalization
  • Severely impaired hearing or speech such that telephone counseling is not possible

Outcomes

Primary Outcomes

smoking, self-report

Time Frame: 6 month follow-up (6 months post-quit attempt)

Participants' self-report of smoking in the past seven days will be measured at 6-month follow-up study visit.

Secondary Outcomes

  • saliva cotinine(3 month follow-up (3 months post-quit attempt))
  • smoking, self-report(3 month follow-up (3 months post-quit attempt))

Study Sites (1)

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