Cognitive-Behavioral Therapy and Hypnotherapy for Smoking Cessation

NCT ID: NCT01129999

Last Updated: 2014-02-04

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

360 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-09-30

Study Completion Date

2013-04-30

Brief Summary

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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.

Detailed Description

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Conditions

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Smoking Cessation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Cognitive-Behavioral Therapy

Group Type EXPERIMENTAL

Cognitive-Behavioral Therapy

Intervention Type BEHAVIORAL

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

Hypnotherapy

Group Type EXPERIMENTAL

Hypnotherapy

Intervention Type BEHAVIORAL

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

Interventions

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Cognitive-Behavioral Therapy

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

Intervention Type BEHAVIORAL

Hypnotherapy

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

Intervention Type BEHAVIORAL

Other Intervention Names

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hypnosis

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Universitätsklinikum Hamburg-Eppendorf

OTHER

Sponsor Role collaborator

University Hospital Tuebingen

OTHER

Sponsor Role lead

Responsible Party

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Anil Batra

Prof. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Anil Batra, Prof.

Role: STUDY_DIRECTOR

University Hospital Tuebingen

Locations

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University Hospital of Tuebingen Smoking Cessation Research Group

Tübingen, , Germany

Site Status

Countries

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Germany

References

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Batra A, Eck S, Riegel B, Friedrich S, Fuhr K, Torchalla I, Tonnies S. Hypnotherapy compared to cognitive-behavioral therapy for smoking cessation in a randomized controlled trial. Front Psychol. 2024 Feb 27;15:1330362. doi: 10.3389/fpsyg.2024.1330362. eCollection 2024.

Reference Type DERIVED
PMID: 38476396 (View on PubMed)

Other Identifiers

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108368

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

DKH-Studie VT-HT

Identifier Type: -

Identifier Source: org_study_id

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