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Anxiety Sensitivity Program for Smoking Cessation

Anxiety Sensitivity Program for Smoking Cessation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00387049
Enrollment
80
Registered
2006-10-12
Start date
2005-01-31
Completion date
2010-04-30
Last updated
2010-10-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation

Keywords

Anxiety Sensitivity

Brief summary

The purpose of this study is to develop and test a smoking cessation intervention for persons who are specifically sensitive to anxiety and anxiety-related bodily sensations.

Interventions

BEHAVIORALAnxiety Sensitivity Program for Smoking Cessation

Sponsors

National Institute on Drug Abuse (NIDA)
CollaboratorNIH
University of Vermont
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Aged between 18 and 65 years old 2. Not pregnant 3. Regular smoker averaging 10 or more cigarettes per day for at least one year 4. Score of 25 or greater on 16-item Anxiety Sensitivity Index 5. Motivation to Quit score of 7 or greater (using Readiness to Quit Ladder) 6. Not currently using pharmacotherapy for smoking cessation (e.g., Zyban) 7. No use of other tobacco products (e.g., chewing tobacco, cigars) 8. No Axis-I or Axis-II diagnoses other than mood or anxiety disorders (intake interview required) 9. No suicidal or homicidal ideation 10. No current psychotropic medication use 11. No evidence of substance abuse or dependence (other than nicotine dependence) 12. No history of significant medical conditions (cardiovascular, neurological, etc.) 13. Ability to provide informed, written consent (no evidence of limited mental capacity) 14. Sufficient command of the English language (able to carry on interview conversation) 15. Plan to stay in Burlington VT area for at least next 6 months

Exclusion criteria

1. Not between 18-65 years old 2. Pregnant or currently trying to become pregnant 3. Regular smoker for less than one year OR smoke less than 10 cigarettes per day 4. ASI below cutoff level of 25 5. Motivation to Quit score of 6 or less (using Readiness to Quit Ladder) 6. Current or recent use of any pharmacotherapy for smoking cessation (e.g., patch, Zyban) 7. Current use of other tobacco products (e.g., chewing tobacco, cigars) 8. Axis-I disorders other than anxiety or mood disorders. 9. Endorsement of suicidality or homicidal ideation. 10. Any current psychotropic medication use (must have stopped at least 1 month prior). 11. Any evidence of substance abuse or dependence (other than nicotine dependence) 12. Any history of significant medical conditions (cardiovascular, neurological, etc.) 13. Inability to provide informed, written consent (evidence of limited mental capacity) 14. Insufficient command of the English language (unable to carry on conversation) 15. Plan to permanently leave Burlington area anytime during the next 6-12 months

Design outcomes

Primary

MeasureTime frame
Smoking status2 weeks post Quit Day

Secondary

MeasureTime frame
Where applicable, length of time from Quit Day to relapse.Determined at conclusion of study

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026