Nicotine Dependence Clinical Trial
— ProjectMISTOfficial title:
Incentives to Promote Smoking Cessation in Low SES Women
NCT number | NCT03173274 |
Other study ID # | 5-24001 |
Secondary ID | |
Status | Terminated |
Phase | N/A |
First received | |
Last updated | |
Start date | February 8, 2018 |
Est. completion date | March 3, 2018 |
Verified date | February 2019 |
Source | Brown University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Terminated |
Enrollment | 1 |
Est. completion date | March 3, 2018 |
Est. primary completion date | March 3, 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
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 |
Country | Name | City | State |
---|---|---|---|
United States | Brown University School of Public Health | Providence | Rhode Island |
Lead Sponsor | Collaborator |
---|---|
Brown University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Percent of negative CO samples | The amount of negative, decreased CO samples submitted by participants | End of two-week intervention |
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