Intervention group (receiving: see below) and control group, receiving usual care.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Gender: Male; 2. Age: 18-55 years; 3. Availability: Available for the study for the following 12 months; 4. Permission: Signed an informed consent form; 5. Health status: at risk for CVD, according to the screening instrument; 6. At risk for CVD according to the Framingham risk score, AND one or more of the following other risk factors: Insufficiently active; Fulfilling none of the Dutch PA standards (NNGB and Fitnorm); Alcohol use; No alcohol at all or > 35 glasses of alcohol per week; HbA1c > 6.5%; BMI >30 kg/m2; Psychological complaints; Tiredness or stress and/or treated for psychological disorders and/or low motivation to recover; Heart complaints: shortness of breath and/or suffering from chest pain and/or diagnosed with or treated for CVD or its predictors (e.g. high blood pressure).
Exclusion criteria
Exclusion criteria: 1. Unable to be physically active; 2. Not sufficiently capable of using the Dutch language; 3. Not having signed an informed consent form.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Dietary intake: a. Fruits, vegetables and fish; b. Sweet and salty snacks, soda, alcohol and sugar intake; c. Slices of bread, plates for dinner; 2. Physical activity: a. Fulfilling the NNGB and the Fitnorm; b. Frequency, duration and intensity of habitual PA in leisure time; 3. Smoking status: Smoker/ non-smoker. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. BMI (kg/ m²); 2. Systolic and diastolic blood pressure (mmHg); 3. HDL-cholesterol and total cholesterol (mmol/liter); 4. HbA1C (%); 5. Cardio respiratory fitness; 6. Stage of change; 7. Behaviour determinants; 8. Perceived general health; 9. Absenteeism; 10. Cost-effectiveness. | — |
Contacts
VU University Medical Center, EMGO-Institute, Van der Boechorststraat 7