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Incentives to Promote Smoking Cessation in Low SES Women (ProjectMIST)

Primary Purpose

Nicotine Dependence

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Brief Motivational Intervention
Contingency Management
Non-Contingent Reinforcement
Sponsored by
Brown University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Nicotine Dependence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18+
  • Smoke an average of at least ten cigarettes per day for at least 1 year
  • Breath CO levels > 8 ppm
  • >12 years of education
  • Reliable and consistent access to a smart phone with video messaging capabilities

Exclusion Criteria:

  • Intention to quit smoking in the next 30 days
  • Currently seeking treatment for smoking cessation.
  • Currently using nicotine replacement therapies or other pharmacotherapies as cessation aid (intermittent use acceptable)
  • No reliable access to a video-messaging smart phone
  • Pregnancy

Sites / Locations

  • Brown University School of Public Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Contingency Management (CM)

Non-Contingent Reinforcement

Arm Description

Those in the CM condition will continue to provide CO values twice-daily, and will receive escalating reinforcement values for CO values indicating continuous smoking abstinence (CO < 6 ppm).

Participants in the NC condition will also provide CO levels twice-daily. However, their reinforcement will not be contingent upon their CO level but will be yoked to someone in the CM condition so that average reinforcer values are equivalent across the 2 conditions.

Outcomes

Primary Outcome Measures

Percent of negative CO samples
The amount of negative, decreased CO samples submitted by participants

Secondary Outcome Measures

Full Information

First Posted
May 24, 2017
Last Updated
February 28, 2019
Sponsor
Brown University
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1. Study Identification

Unique Protocol Identification Number
NCT03173274
Brief Title
Incentives to Promote Smoking Cessation in Low SES Women
Acronym
ProjectMIST
Official Title
Incentives to Promote Smoking Cessation in Low SES Women
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Terminated
Why Stopped
Grant funding ended for pilot work
Study Start Date
February 8, 2018 (Actual)
Primary Completion Date
March 3, 2018 (Actual)
Study Completion Date
March 3, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brown University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The purpose of this study is to investigate the feasibility of a mobile-phone based contingency management (CM) intervention for smoking in low-SES women. The CM intervention will be combined with a Brief Motivational Interviewing (BMI) counseling component. This study will examine the following research aims: Primary Aim: To compare the effects of a Brief Motivational Intervention (BMI) + mobile phone-based CM on tobacco use when compared to BMI with a non-contingent control condition in a small feasibility trial. Hypothesis: The investigators expect women in the BMI + CM condition to have more smoke free days than women in the BMI + NC condition. Secondary Aim: To examine alcohol use as a moderator of cessation outcomes.
Detailed Description
Cigarette smoking is the leading cause of preventable death in the United States, accounting for one out of every five deaths (CDC, 2012). In particular, smoking prevalence rates are high among socioeconomically-disadvantaged women; for example, over 40% of women with less than 12 yrs education smoke, compared to 28% and 16% among those with some college and undergraduate degrees (SAMHSA, 2010). Smoking cessation rates are particularly low among low-SES women with co-occurring alcohol use disorders, and these substances are frequently used together (Kahler et al., 2010; Businelle et al., 2013). Therefore, interventions that reduce both alcohol and smoking among heavy alcohol-using women are vitally needed to reduce rates of smoking-related morbidity and mortality in this vulnerable population. Counseling approaches that incorporate problem solving, skills training and social support are effective for reducing smoking in the general population (Fiore et al., 2008). However, given the high rates of smoking among alcohol-using women, they may be inadequate for in this population. Contingency management (CM) interventions, which provide tangible reinforcers contingent upon smoking abstinence or reduction to a criterion level, are highly-efficacious interventions for reducing cigarette smoking and other drug use in low-SES women (Higgins et al., 2012). Within the theoretical framework of operant conditioning, increasing the availability of an alternative reinforcer weakens the amount of control that the drug has over the user's behavior, especially when obtaining the alternative reinforcer is contingent on behaviors incompatible with drug use (Higgins, 1997). The tenets of CM interventions include (1) arranging the environment such that the target behavior can be readily and objectively detected, (2) providing a tangible reinforcer when the target behavior occurs, and (3) withholding reinforcement when the target behavior does not occur (Higgins et al., 1994). Although CM interventions clearly are effective at promoting smoking reductions, there are several challenges associated with translating CM into an effective clinical treatment for smoking. Perhaps the most significant challenge is the frequent monitoring necessary to objectively verify smoking abstinence using breath carbon monoxide (CO), the most convenient objective measure of smoking status. Because of the short half-life of CO (5-6 hours), CO levels must be measured at least twice per day in order to verify continuous abstinence. Recent CM-smoking studies have addressed this feasibility challenge by providing study participants with breath CO monitors and laptop computers or smartphones to use in their own natural environments (e.g., Dallery, Raiff & Grabinski, 2013). Participants are taught how to use their smartphones to text videos of themselves providing a breath CO level to a research staff member, twice per day. After the study staff has determined that the breath CO sample meets the abstinence criterion, participants are informed of the amount that they have earned for that sample. Given the high rates of smoking in low-SES women, investigating the additive impact of an in-person brief counseling intervention and a phone-based CM intervention is an important next step in examining effective methods to reduce the impact of smoking in this population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nicotine Dependence

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
1 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Contingency Management (CM)
Arm Type
Experimental
Arm Description
Those in the CM condition will continue to provide CO values twice-daily, and will receive escalating reinforcement values for CO values indicating continuous smoking abstinence (CO < 6 ppm).
Arm Title
Non-Contingent Reinforcement
Arm Type
Active Comparator
Arm Description
Participants in the NC condition will also provide CO levels twice-daily. However, their reinforcement will not be contingent upon their CO level but will be yoked to someone in the CM condition so that average reinforcer values are equivalent across the 2 conditions.
Intervention Type
Behavioral
Intervention Name(s)
Brief Motivational Intervention
Intervention Description
Participants in both groups will be given an BMI intervention in which they will be counseled to quit smoking.
Intervention Type
Behavioral
Intervention Name(s)
Contingency Management
Intervention Description
Contingent Reinforcement for negative breath CO samples
Intervention Type
Behavioral
Intervention Name(s)
Non-Contingent Reinforcement
Intervention Description
Participants will receive reinforcement for submitting samples ona yoked schedule unrelated to CO sample value [CM control]
Primary Outcome Measure Information:
Title
Percent of negative CO samples
Description
The amount of negative, decreased CO samples submitted by participants
Time Frame
End of two-week intervention

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18+ Smoke an average of at least ten cigarettes per day for at least 1 year Breath CO levels > 8 ppm >12 years of education Reliable and consistent access to a smart phone with video messaging capabilities Exclusion Criteria: Intention to quit smoking in the next 30 days Currently seeking treatment for smoking cessation. Currently using nicotine replacement therapies or other pharmacotherapies as cessation aid (intermittent use acceptable) No reliable access to a video-messaging smart phone Pregnancy
Facility Information:
Facility Name
Brown University School of Public Health
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02912
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Incentives to Promote Smoking Cessation in Low SES Women

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