ClinicalTrials.Veeva

Menu

Comparison of Four Different Smoking Cessation Programmes (Fristart)

University of Southern Denmark (SDU) logo

University of Southern Denmark (SDU)

Status

Unknown

Conditions

Self-efficacy
Smoking
Smoking Cessation

Treatments

Device: Interactive web-based smoking cessation programme
Device: Proactive telephone counselling
Device: Standard 15-minute telephone counselling
Device: Self-help material

Study type

Interventional

Funder types

Other

Identifiers

NCT01487642
NIPH-2066

Details and patient eligibility

About

The primary objective of the study is to compare the efficacy of four different smoking cessation programmes, including a proactive telephone counseling intervention, a reactive telephone counseling a and an interactive web-based intervention and (as control) written self-help material.

Full description

Smoking remains the most important threat to public health. The majority of smokers wish to quit smoking and every year a substantial part of smokers makes a quit attempt. However, the majority of smokers tries to quit unassisted and existing smoking cessation interventions are underused. In this study we test the effectiveness of four different smoking cessation interventions in a randomized controlled trial. The study provides knowledge on factors important for recruitment and gives indication on potential reach of interventions among the general population. This knowledge can help us in designing interventions that is both effective but also have a high reach in the general population.

Enrollment

1,600 estimated patients

Sex

All

Ages

16+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged 16 and older
  • Current smoker: Willing to quit smoking within the next 12 weeks
  • Having a regular access to Internet
  • Having a personal e-mail address
  • Having a personal mobile cell phone with a Danish number
  • Given informed consent
  • Can read and understand Danish

Exclusion criteria

  • Less than 16 years of age
  • No personal e-mail address
  • No personal mobile cell phone
  • Not able to give informed consent

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

1,600 participants in 4 patient groups

Telephone counselling
Experimental group
Treatment:
Device: Standard 15-minute telephone counselling
Device: Proactive telephone counselling
Proactive telephone counselling
Experimental group
Treatment:
Device: Proactive telephone counselling
web-based smoking cessation programme
Experimental group
Treatment:
Device: Interactive web-based smoking cessation programme
Self-help material
Active Comparator group
Treatment:
Device: Self-help material

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems