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Telephone-based Treatment for Smoking Cessation

Motivational Interviewing in Smoking Cessation: A Controlled Clinical Trial at the Swedish National Tobacco Quitline

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01121887
Enrollment
1309
Registered
2010-05-12
Start date
2005-01-31
Completion date
2007-10-31
Last updated
2010-05-12

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, telephone counselling, motivational interviewing, treatment integrity, Tobacco Smoking

Brief summary

Aim: to assess the effect of adding Motivational Interviewing (MI) to the existing smoking cessation treatment protocol at the Swedish National Tobacco Quitline (SNTQ). Methods: Experienced counsellors at SNTQ either received further training in the standard treatment (ST) protocol (including Cognitive Behavioural Therapy (CBT)) or a comprehensive regime of training in MI. 1309 clients were randomized to either the ST group or the group with MI added to the treatment protocol. In order to ensure treatment integrity among counsellors, MI skill was assessed using the Motivational Interviewing Treatment Integrity Code (MITI).

Interventions

BEHAVIORALStandard treatment

Telephone-based smoking cessation counselling based on a combination of coaching and cognitive behavioural therapy (CBT) techniques. Counsellors are also trained in giving tailored advice regarding the use of smoking cessation aids. Clients are offered a choice between reactive treatment (clients initiate all contact) and proactive treatment (counsellors call back at appointed dates). Printed information material tailored to clients' needs is offered free of charge.

BEHAVIORALMotivational Interviewing

Telephone-based smoking cessation counselling with Motivational Interviewing added to the standard treatment protocol. Clients are offered a choice between reactive treatment (clients initiate all contact) and proactive treatment (counsellors call back at appointed dates). Printed information material tailored to clients' needs is offered free of charge.

Sponsors

Region Stockholm
CollaboratorOTHER_GOV
Karolinska Institutet
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Clients have to express a desire for support regarding smoking cessation * Clients have to be willing to confirm their identity by answering a baseline registration questionnaire

Exclusion criteria

* Clients with obvious difficulties understanding Swedish * Clients with obvious mental impairments * Clients using tobacco products other than cigarettes (mainly smokeless tobacco, or snus)

Design outcomes

Primary

MeasureTime frameDescription
Point prevalence abstinence12 months after initial contact with SNTQNot one puff of smoke during the previous 7 days

Secondary

MeasureTime frameDescription
Continuous abstinence12 months after initial contact with SNTQNot a single puff of smoke within the past six months or more

Countries

Sweden

Outcome results

None listed

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