Comparing two e-Health programs for the GP-setting to target LSES and HSES smokers.

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON21954

Enrollment

1500

Registered

2011-10-12

Start date

2010-12-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

smoking cessation, web-based tailored intervention

Interventions

Intervention: Respondents in the multiple tailoring group (two experimental groups) will receive multiple computer tailoring feedback on different moments: Depending on a person's intention to quit s

Eligibility

Inclusion criteria

Inclusion criteria: 1. Smoke; 2. Are 18 years or older; 3 Are able to understand Dutch sufficiently.

Exclusion criteria

Exclusion criteria: 1. Do not smoke; 2. Are younger than 18 years; 3. Are not able to understand Dutch sufficiently; 4. Respondents that refuse to sign the informed consent form are also excluded from participation.

Design outcomes

Primary

Measure	Time frame
1. 7-day point prevalence abstinence from smoking (PPA); 2. Continued abstinence.	—

Secondary

Measure	Time frame
1. 24-hour point prevalence; 2. Smoking during the last month; 3. Number of quit attempts; 4. Overall tobacco consumption; 5. Self-efficacy; 6. Attitudes; 7. Intention to quit smoking.	—

Contacts

Public ContactN.E. Stanczyk

Postbus 616 6200 MD

nicola.stanczyk@maastrichtuniversity.nl+31 (0)43 3882379

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)