Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
46 participants
INTERVENTIONAL
2016-07-01
2019-09-27
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Intensive Referral Intervention Group
Intensive Referral Intervention will by done by trained probation officers
Intensive Referral Intervention Group
The Intensive Referral Intervention Group will review a series of pamphlets regarding participation in 12-step meetings as well as smoking cessation that will be presented in a group setting to probationers in 3 sessions.
Standard Practice Facilitated Group
Standard Current Practice will be provided by untrained probation officers
Standard Practice Facilitated Group
The Standard Practice Facilitated Group will receive 3 sessions of the current standard practice for facilitated groups.
Interventions
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Intensive Referral Intervention Group
The Intensive Referral Intervention Group will review a series of pamphlets regarding participation in 12-step meetings as well as smoking cessation that will be presented in a group setting to probationers in 3 sessions.
Standard Practice Facilitated Group
The Standard Practice Facilitated Group will receive 3 sessions of the current standard practice for facilitated groups.
Eligibility Criteria
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Inclusion Criteria
* SUD
* daily cigarette smoker
Exclusion Criteria
* unwilling to provide personal contact information
* unable to pass Mini-Cog
19 Years
ALL
No
Sponsors
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University of Nebraska
OTHER
Responsible Party
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Principal Investigators
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Kathleen M Grant, MD
Role: PRINCIPAL_INVESTIGATOR
University of Nebraska
Locations
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Unversity of Nebraska Medical Center
Omaha, Nebraska, United States
Countries
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Other Identifiers
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0018-16-FB
Identifier Type: -
Identifier Source: org_study_id
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