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Nurse-led Smoking Cessation With Further Follow-up in Lifestyle Centres - a Randomized Pilot Study

V

Vestre Viken Hospital Trust

Status

Completed

Conditions

Cardiovascular Diseases
Smoking Behaviors
Nurse's Role
Smoking Cessation

Treatments

Behavioral: behavioural and cessation aids

Study type

Interventional

Funder types

Other

Identifiers

NCT04772144
REK 202686

Details and patient eligibility

About

The purpose of this randomized controlled pilot study is to test whether an in-hospital nurse-led smoking cessation intervention increases the refferal rate to healty life-centers in the municipalities. We will also describe the proportion who succeed in quitting smoking between the intervention group and the control group and obtain new knowledge about the patient and system factors of importance for participation to healty life-centers and for successful and unsuccessful smoking cessation.

Enrollment

58 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (all):

  • Age> 18 years and smokes at least 1 cigarette daily
  • Hospitalized with a cardiovascular event (i.e. myocardial infarction, heart failure, unstable or stable angina, achyarrhythmias, bradyarrhythmias, carotid stenosis or claudication with need for peripheral revascularization)
  • Sign informed consent and is expected to participate according to ICH / GCP

Exclusion Criteria (none of these):

  • Does not meet the criteria to participate in the pilot project, i.e. patients who do not usually live or work in the Vestre Viken catchment area

  • Chronic renal failure stage 4 or known allergic reaction to varenicline

    . Any condition (e.g. psychosis, alcohol abuse, dementia) or situation that may pose a significant risk to the participant, confuse the results or make participation unethical

  • Lack of Norwegian and English knowledge

  • Short life expectancy (<12 months)

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

58 participants in 2 patient groups

Intervention group
Experimental group
Treatment:
Behavioral: behavioural and cessation aids
Control group
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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