Actively Recruiting
Smoking Cessation Behavioral Treatment Study
Led by University of Missouri-Columbia · Updated on 2024-08-07
200
Participants Needed
2
Research Sites
275 weeks
Total Duration
On this page
Sponsors
U
University of Missouri-Columbia
Lead Sponsor
M
Medical University of South Carolina
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to evaluate the effectiveness of two behavioral interventions on smoking behavior - Mindfulness-Oriented Recovery Enhancement (MORE) and Cognitive Behavioral Therapy (CBT). MORE is a behavioral therapy that integrates mindfulness training to modify reward processes. CBT is a therapy designed to help individuals understand how their thoughts and feelings influence their behaviors.
CONDITIONS
Official Title
Smoking Cessation Behavioral Treatment Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 and up
- Fluency in English to provide informed consent and follow study tasks independently
- Functional vision, with corrective lenses if needed, to complete assessments and tasks
- Current nicotine-dependent smoker with at least 2 years of smoking history
- Interest in quitting smoking
You will not qualify if you...
- Use of psychotropic medications (e.g., antiepileptics) in the past month
- Positive urine drug screen
- Presence of untreated medical illness
- Current or past psychosis
- History of major neurological illness or head injury with loss of consciousness
- Contraindications to MRI, including claustrophobia
- Positive urine pregnancy test among females
- Inability or unwillingness to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University of Missouri - Columbia
Columbia, Missouri, United States, 65211
Actively Recruiting
2
Medical University of South Carolina
Charleston, South Carolina, United States, 29425
Not Yet Recruiting
Research Team
M
Madhura Athreya, MS
CONTACT
B
Brett Froeliger, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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