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The ZWOlle Transmural Integrated Care for CArdiovaScular Risk Management Study

The ZWOlle Transmural Integrated Care for CArdiovaScular Risk Management Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03428061
Acronym
ZWOT-CASE
Enrollment
740
Registered
2018-02-09
Start date
2017-09-01
Completion date
2018-03-31
Last updated
2018-02-09

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

Conditions

Cardiovascular Diseases, Hypercholesterolemia, Hypertension

Keywords

Prevention, Disease Management, Integrated care, Primary Health Care

Brief summary

Cardiovascular disease (CVD) contributes importantly to mortality and morbidity. Prevention of CVD by lifestyle change and medication is important and needs full attention. In the Netherlands an integrated program for cardiovascular risk management (CVRM), based on the Chronic Care Model (CCM), has been introduced in many regions in recent years, but evidence from studies that this approach is beneficial is very limited. In the ZWOT-CASE study the investigators will assess the effect of integrated care for CVRM in the region of Zwolle on two major cardiovascular risk factors: systolic blood pressure (SBP) and low-density lipoprotein cholesterol (LDL-cholesterol) in patients with or at high risk of CVD. This study is a pragmatic clinical trial comparing integrated care for CVRM with usual care among patients aged 40-80 years with CVD (n= 370) or with a high CVD risk (n= 370) within 26 general practices. After one year follow-up, primary outcomes (SBP and LDL-cholesterol level) are measured. Secondary outcomes include lifestyle habits (smoking, dietary habits, alcohol use, physical activity), risk factor awareness, 10-year risk of cardiovascular morbidity or mortality, health care consumption, patient satisfaction and quality of life.

Interventions

OTHERIntegrated care for cardiovascular risk management

Disease management program for the prevention of cardiovascular diseases

Sponsors

Isala
CollaboratorOTHER
Medrie Health Care Group, Zwolle
CollaboratorUNKNOWN
Hein Hogerzeil Stichting
CollaboratorUNKNOWN
UMC Utrecht
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years

Inclusion criteria

for patients with CVD: * Patients with a history of atherosclerotic CVD defined as documented angina pectoris, myocardial infarction, chronic ischemic heart disease, coronary sclerosis, transient ischaemic attack (TIA), cerebral infarction, intermittent claudication or aneurysm of the abdominal aorta * The CV risk of the patient is managed in primary care, not in the hospital or outpatient clinic by a medical specialist * Age between 40 and 80 years Inclusion criteria for high risk patients: * Use of blood pressure lowering or lipid lowering drugs * A 10 -years CV risk \> 10%, based on the Dutch guideline for CVRM and i) either 1 strongly cardiovascular risk enhancing factor or 2 mildly cardiovascular risk enhancing factors (see table 6) or ii) \> 1 CV risk factor (current smoking, SBP\>140 mmHg, LDL\>2.5 mmol/L, TC/HDL-ratio \> 8, chronic renal impairment (age \< 65 years: eGFR \< 60 ml/min/1,73 m2; age ≥ 65 years: eGFR \< 45 ml/min/1,73 m2, and/or (micro)albuminuria). * A 10-year CV risk of \>20% and \> 1 CV risk factor (current smoking, SBP\>140 mmHg, LDL\>2.5 mmol/L, TC/HDL-ratio \> 8, chronic renal impairment (age \< 65 years: eGFR \< 60 ml/min/1,73 m2; age ≥ 65 years: eGFR \< 45 ml/min/1,73 m2, and/or (micro)albuminuria). * The CV risk of the patient is managed in primary care, not in the hospital or outpatient clinic by a medical specialist * Age between 40 and 80 years

Exclusion criteria

for all patients: * Diabetes mellitus, as these patients are already included in a disease management program for diabetes mellitus * Limited life expectancy, as assessed by the GP * Cognitive impairment, as assessed by the GP * No Dutch language proficiency * Staying abroad for longer than three months during the duration of the study. * The CV risk of the patient is managed in the hospital or outpatient clinic by a medical specialist

Design outcomes

Primary

MeasureTime frameDescription
Systolic blood pressureAfter 1 year of follow-upSystolic blood pressure, manual or electronic oscillometric measurement, at least 2 measurements with an interval of 1-2 minutes
LDL-cholesterolAfter 1 year of follow-upBlood sample

Secondary

MeasureTime frameDescription
Body mass index (BMI)After 1 year of follow-upThe BMI is defined as the body mass divided by the square of the body height, and is expressed in units of kg/m2, resulting from mass in kilograms and height in metres. BMI will be measured by the general practitioner or practice nurse during the endpoint visit
Healthy dietAfter 1 year of follow-upHealthy diet yes or no according to the Dutch guideline for cardiovascular risk management and national guideline for healthy diet ((daily 150 - 200 grams vegetables and 200 grams fruit; daily 30 - 40 grams dietary fibers; twice a week 100 - 150 gram fish, at least once fatty fish; maximum of 6 grams salt per day; maximum of 2 (men) or 1 (women) alcohol consumptions per day). Food habits will be measured by a questionairre.
Physical activityAfter 1 year of follow-upSquash questionnaire
Motivation to quit smokingAfter 1 year of follow-upMotivation to quit smoking: motivated to quit/not motivated to quit/ considers to quit smoking
Awareness of received lifestyle advicesAfter 1 year of follow-upAware/ not aware of received lifestyle advices, measured by questionairre
Awareness of food habitsAfter 1 year of follow-upPatient will be asked whether he/she thinks if he/she has healthy food habits yes or no. Measured by a questionairre
Awareness of physical activityAfter 1 year of follow-upPatient will be asked whether he/she thinks if he/she has a healthy level of physical activity yes or no. Measured by a questionairre
Awareness of weightAfter 1 year of follow-upPatient will be asked whether he/she thinks if he/she has a healthy weight yes or no. Measured by a questionairre
Awareness of hyperlipidaemiaAfter 1 year of follow-upPatient will be asked whether he/she thinks if he/she has hyperlipidaemia yes or no. Measured by a questionairre
Awareness of cardiovascular disease riskAfter 1 year of follow-upEstimation by patient of his/her own cardiovascular disease risk by a questionairre
Awareness of hypertensionAfter 1 year of follow-upPatient will be asked whether he/she thinks if he/she has hypertension yes or no. Measured by a questionairre
Use of adequate antihypertensivesAfter 1 year of follow-upUse of adequate antihypertensives according to Dutch guideline for cardiovascular risk management. Measured by medication registered in electronic medical records in general practice
Use of adequate lipid lowering drugsAfter 1 year of follow-upUse of adequate lipid lowering drugs according to Dutch guideline for cardiovascular risk management. Measured by medication registered in electronic medical records in general practice
Use of adequate anticoagulantsAfter 1 year of follow-upUse of adequate anticoagulants according to Dutch guideline for cardiovascular risk management. Measured by medication registered in electronic medical records in general practice
10-years cardiovascular morbidity or mortality riskAfter 1 year of follow-up10-years cardiovascular morbidity or mortality risk (percentage) (Risk chart Dutch guideline or SMART risk score)
Newly developed diabetes mellitusAfter 1 year of follow-upNewly developed diabetes mellitus, based on coded diagnosis in electronic medical record in general practice
Newly developed COPDAfter 1 year of follow-upNewly developed COPD, based on coded diagnosis in electronic medical record in general practice
Newly developed heart failureAfter 1 year of follow-upNewly developed heart failure, based on coded diagnosis in electronic medical record in general practice
Newly developed atrial fibrillationAfter 1 year of follow-upNewly developed atrial fibrillation, based on coded diagnosis in electronic medical record in general practice
MortalityAfter 1 year of follow-upDied due to cardiovascular disease or other cause
Primary treating practitioner in the context of cardiovascular risk managementAfter 1 year of follow-upGeneral practitioner or medical specialist.
Health care consumption in the past yearAfter 1 year of follow-upConsultations in the contect ox cardiovascular risk management in general practice
Self-management in the past yearAfter 1 year of follow-upPatient Activity Measure (PAM)
Self-measurements of blood pressure in the past yearAfter 1 year of follow-upSelf-measurements of blood pressure in the past year yes or no
Patient satisfaction regarding the provided care in the past yearAfter 1 year of follow-upPatient Reported Experience Measure (PREM)
Quality of lifeAfter 1 year of follow-upEQ-5D
Anxiety and depressionAfter 1 year of follow-upHospital Anxiety and Depression Scale (HADS), 0-7: no depression or anxiety, 8-10: depression or anxiety is possible,11-21: depression or anxiety is likely
Cost-efficiencyAfter 1 year of follow-upiPCQ
MorbidityAfter 1 year of follow-upNewly developed cardiovascular diseases
Smoking statusAfter 1 year of follow-upSmoking yes or no

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026