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Cognitive-Behavioral Therapy and Hypnotherapy for Smoking Cessation

The Comparative Efficacy of Cognitive-Behavioral Therapy (CBT) and Hypnotherapy (HT) for Smoking Cessation.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01129999
Acronym
CBT-HT
Enrollment
360
Registered
2010-05-25
Start date
2010-09-30
Completion date
2013-04-30
Last updated
2014-02-04

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

Conditions

Smoking Cessation

Keywords

smoking cessation, CBT, hypnotherapy

Brief summary

Intensive cognitive-behaviour interventions (CBT) combined with pharmacotherapy for smoking cessation are well established and have been proved to be efficacious. Nevertheless, they yield only long-term abstinence rates about 35%. Considering the high interest of smokers in alternative medicine, the availability of a broad range of treatment methods, of which smokers choose an intervention according to their preferences, might contribute to improve treatment outcome. While hypnotherapy (HT) is an already widely promoted alternative method for aiding cessation, considerable methodological shortcomings of studies on this topic limit the interpretability of the results. In 2006, the German Academic Advisory Committee for Psychotherapy released new guidelines that included HT as an acceptable treatment for smoking cessation. The committee conceded, however, that conclusions concerning its efficacy are restricted due to the heterogeneity of findings. Hence, further well-designed studies are required to better test the efficacy of HT in comparison to accepted treatments. This randomised, controlled trial aims to compare the efficacy of CBT and HT for smoking cessation. Further, the influence of moderating variables will be investigated. It is hypothesized that 1) participants receiving CBT will evince higher abstinence rates than those receiving HT, 2) levels of nicotine dependence, self-efficacy and motivation to change will moderate the intervention effects and 3) participants with high levels of suggestibility will evince higher abstinence rates in the HT-intervention compared to participants with low levels of suggestibility. 220 adult healthy smokers will be randomized to receive either CBT or HT. Both programmes will be conducted in 6, weekly, 90-minute group sessions. Participants will be followed up at 1, 3, 6, 9 und 12 month post-treatment. Generalized estimating equation models will be conducted to analyse group differences on abstinence rates. The models will include the above mentioned moderator variables.

Interventions

BEHAVIORALCognitive-Behavioral Therapy

a cognitive-behavioral smoking cessation program; 6, weekly-held, group sessions (90 min each)

BEHAVIORALHypnotherapy

hypnotherapeutic smoking cessation program; 6, weekly-held, group sessions (90 min each)

Sponsors

Universitätsklinikum Hamburg-Eppendorf
CollaboratorOTHER
University Hospital Tuebingen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* at least 18 years of age * smoking at least 10 cigarettes per day * smoking at least for the past two years * fluency in German language * willing and able to give written informed consent

Exclusion criteria

* women: planned or current pregnancy or breast-feeding * participation in a smoking cessation program within the last 6 months * severe mental illness

Design outcomes

Primary

MeasureTime frame
12-months continuous smoking abstinence according to the Russell Standard (RS; West et al. 2005)12-months follow-up

Secondary

MeasureTime frame
7-day point-prevalence smoking abstinence rates at 6- and 12-months follow-up12-months follow-up

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026