SPRING-study: Efficacy of paramedical use of software-guided cardiovascular prevention programs in a first-line general practitioner setting, comparison of care provided via telemonitoring or within general practice setting.

SPRING-study: Efficacy of paramedical use of software-guided cardiovascular prevention programs in a first-line general practitioner setting, comparison of care provided via telemonitoring or within general practice setting. - SPRING study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON30952

Enrollment

400

Registered

2008-01-22

Start date

2007-11-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

moderate cardiovascular risk

Interventions

Participants receive medication and lifestyle advice from a nurse practitioner over the year. With the intervention group this is accompanied by intensive feedback based on and home monitoring devic

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - men 50-75 yr, females 55-75 yr - BMI >= 25 or smokers or low physical activity - SCORE-score >= 5% - able to use simple home monitoring devicesr

Exclusion criteria

Exclusion criteria: - not motivated fo lifestyle intervention - known cardiovascular disease - known diabetes - thyroid function abnormality - life expectancy

Design outcomes

Primary

Measure	Time frame
Change in SCORE-score after one year of treatment.	—

Secondary

Measure	Time frame
- Change in specific risk facors (blood pressure, cholesterol, physical activity, weight, waist circumference, smoking habits) - Psychological wellness - Patient satisfaction - Cost effectivity - AGE	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)