Skip to content

SUCCESS STUDY; Smoking reduction by a smoking cessation strategy in the national cervical cancer screening program

SUCCESS STUDY; Smoking reduction by a smoking cessation strategy in the national cervical cancer screening program - SUCCESS STUDY

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON44561
Enrollment
660
Registered
2017-12-21
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

tabaksverslaving cervical cancer screening smoking cessation

Interventions

1. Providing information about the role of smoking in the development of cervical cancer 2. Offering an appointment with the practice nurse or general practitioner for smoking cessation support

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all of the following criteria: - Participating in the national cervical cancer screening program, i.e. undergoing a cervical smear at a general practice included in the study, upon invitation from the national cervical screening program organization. This includes those women undergoing a smear after they are found to be HPV-positive after a self-test provided by the national cervical cancer screening organization. - Able to communicate in Dutch. - Given informed consent for participation in a study about lifestyle. ;In order to be identified as a smoker, a subject must meet one of the following criteria: - Daily or non-daily smokers who participate in cervical cancer screening, identified at baseline via the baseline questionnaire T1 or upon inquiry from the practice assistant about the screening participants* smoking status

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: - Undergoing a cervical smear at the general practice NOT upon an invitation from the national cervical screening program organization. - Not able to communicate in Dutch.

Design outcomes

Primary

MeasureTime frame
The primary outcome includes performing a serious quit attempt (any attempt lasting >24 hours). The percentage of smoking participants (at baseline) who performed a serious quit attempts during the follow-up period will be measured.

Secondary

MeasureTime frame
Secondary outcomes include the total number of quit attempts per participants. The point prevalence abstinence will be measured (defined as not smoking during the last 7 prior to filling in the questionnaire at 6 months follow-up). The total number of smoked cigarettes per day (reduction in number of cigarettes) and the transition in stage of change, e.g. change of motivation to quit smoking, will be measured.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)