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
22 participants
INTERVENTIONAL
2014-03-31
2015-06-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Distress Tolerance Treatment for Weight Concern (DT-W)
DT-W is delivered over a 9 week period with 1 1-hr individual session during week 1, 8 weekly 1.5-hr group counseling sessions during weeks 2-9, and 1 20-minute individual telephone session during week 4. Session content includes distress tolerance intervention for weight concern plus standard behavioral smoking cessation treatment. Participants also receive 8 weeks of nicotine patch.
Distress Tolerance Treatment for Weight Concern (DT-W)
Health Education (HE)
HE is delivered over a 9 week period with 1 1-hr individual session during week 1, 8 weekly 1.5-hr group counseling sessions during weeks 2-9, and 1 20-minute individual telephone session during week 4. Session content includes smoking health education program plus standard behavioral smoking cessation treatment. Participants also receive 8 weeks of nicotine patch.
Health Education (HE)
Interventions
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Distress Tolerance Treatment for Weight Concern (DT-W)
Health Education (HE)
Eligibility Criteria
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Inclusion Criteria
* 18 to 65 years of age
* smoke 10 or more cigarettes per day
* daily smoker for at least the past year
* report motivation to quit smoking in the next month of at least 5 on a 10 point scale
* report concern of at least 50 on at least one of two 100 point scales assessing weight concern
* able to travel to study location for study appointments
Exclusion Criteria
* current use of other tobacco products at least weekly
* current diagnosis of depression
* diagnosis or treatment for non-nicotine substance use disorder with substance use during the past 6 months
* lifetime diagnosis or treatment of eating disorder, bipolar disorder, schizophrenia, or schizoaffective disorder
* current use of psychotropic medication except antidepressants
* score above established cut-offs on self-report screening measures of depressive symptomology, eating disorder symptomology, alcohol use disorder, or drug use disorder
* current suicidality or homicidality
* medical condition that is a contraindication for the use of transdermal nicotine patch
* lives at same address as current or past participant
18 Years
65 Years
FEMALE
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
Butler Hospital
OTHER
Responsible Party
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Principal Investigators
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Erika L. Bloom, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
Butler Hospital and Rhode Island Hospital
Locations
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Butler Hospital
Providence, Rhode Island, United States
Countries
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Other Identifiers
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1303-003
Identifier Type: -
Identifier Source: org_study_id