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Computerized Anger-Reduction Treatment for Smoking Cessation

Computerized Anger-Reduction Treatment for Smoking Cessation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02413814
Enrollment
100
Registered
2015-04-10
Start date
2015-04-01
Completion date
2019-07-30
Last updated
2021-01-28

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

Conditions

Anger, Smoking Cessation

Brief summary

Problematic anger is a strong predictor of failed attempts at smoking cessation. The investigators proposed study seeks to evaluate whether a novel 8-session computerized anger-reduction treatment improves quit rates among smokers. Smokers with elevated trait anger will be administered transdermal nicotine patch therapy and either anger-reduction treatment or a control intervention. They will be assessed throughout treatment and up until three months after a scheduled mid- treatment quit date. The investigators propose to test whether, compared to the control condition, the anger-reduction treatment will lead to: 1) greater reductions in anger and 2) greater abstinence rates at post-cessation and at follow-up assessments. The investigators will also test whether changes in anger-related symptoms account for group differences in abstinence rates.

Detailed description

The current proposal seeks to evaluate an eight-session, computerized, anger-focused intervention for smokers (Anger Reduction Treatment or ART). The investigators will administer this intervention to smokers (N = 114) who are interested in quitting and have elevated levels of trait anger. Participants will be randomly assigned to receive either: (1) computerized ART, consisting of interpretation bias modification, or (2) a computerized control condition, which consists of health education and relaxing video clips. The computerized sessions (eight total) will take place twice a week for four weeks. All participants will have a scheduled quit date for the beginning of the third week of treatment (i.e., at mid-treatment). All participants will also receive nicotine patch therapy to use at their scheduled quit date. Anger symptoms, smoking cravings, and smoking frequency will be assessed throughout treatment. Smoking status, anger, and other measures of negative affect will also be assessed at baseline and regularly for 12-weeks following the scheduled quit date. The investigators will test whether, compared to the control condition, the anger-reduction treatment will lead to: 1) greater reductions in anger and 2) greater abstinence rates at post-cessation and at follow-up assessments. The investigators will also test whether changes in anger-related symptoms account for group differences in abstinence rates.

Interventions

Eight 30-minute sessions of interpretation modification to reduce angry interpretation biases.

BEHAVIORALControl Condition

Eight 30-minute sessions of informative videos on healthy living and relaxation videos.

Sponsors

Florida State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

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

Inclusion criteria

* Elevated levels of trait anger (scoring 22 or higher on the STAXI-trait) * Currently smoking an average of 8 cigarettes per day * Must be a regular (daily) smoker for at least 1 year * Willing to make a serious attempt to quit smoking * Must report motivation to quit in the next month (30 days) of at least 5 on a 10 point scale (0 = no motivation and 10 = extreme motivation) * Have not decreased the number of cigarettes by more than half in the past six months * Must be an English speaker

Exclusion criteria

* Current substance dependence (excluding nicotine dependence) * Current use of other tobacco products * Currently receiving cognitive therapy or therapy for problematic anger * Evidence of serious suicidal intent requiring hospitalization or immediate treatment * Limited mental competency and the inability to give informed, written consent * Evidence of psychotic-spectrum disorders * Changes in medication over the last month

Design outcomes

Primary

MeasureTime frame
State-Trait Anger Expression Inventory-2 (STAXI-2; Spielberger, 1999) state and trait subscalesup to 14-weeks following treatment initiation.
Self-reported smoking frequencyup to 14-weeks following treatment initiation.
Carbon monoxide levelsup to 14-weeks following treatment initiation.

Secondary

MeasureTime frame
WSAP-Hostility Scale (Dillon, Cougle, & Fincham, 2015)up to 14-weeks following treatment initiation.
Minnesota Nicotine Withdrawal Scale (Hughes & Hatsukami, 1986)up to 14-weeks following treatment initiation.
Questionnaire of Smoking Urges (Tiffany & Drobes, 1991)up to 14-weeks following treatment initiation.
Hostile Automatic Thoughts Scale (Snyder, Crowson, Houston, Kurylo, & Piorier, 1997)up to 14-weeks following treatment initiation
Beck Depression Inventory-II (Beck, Steer, & Brown, 1996)Baseline and regularly for 14-weeks following treatment initiation.
Clinical Anger Scale (CAS; Snell, Gum, Shuck, Mosley, & Hite, 1995)up to 14-weeks following treatment initiation.

Countries

United States

Outcome results

None listed

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