Clinical Trials in Norway / NCT06738381
Recruiting Not applicable

Digital Secondary Prevention After Atherosclerotic Cardiovascular Disease

NCT06738381 · tracked via the Priya Life Science Norway tracker
Phase
Not applicable
Started
2025-02-03
Last updated
2025-02-21

Condition(s) studied

Atheroscleroses, CoronaryAtheroscleroses, CerebralAtherosclerotic Ischemic Disease

Investigational drug(s) / intervention(s)

Digital intervention and motivational counselling

Digital intervention and motivational counselling: A single sesstion of motivational interviewing and access to a digital plattform for a six months period

Study summary

Atherosclerotic cardiovascular disease (ASCVD) remains a leading cause of morbidity and mortality worldwide and in Norway. Approximately 50% of the patients admitted to hospitals with an acute ASCVD event has had a previous event. The high number of patients being readmitted to hospitals with new ASCVD events is to a large degree explained by poor control of established risk factors such as high LDL-cholesterol, high blood pressure (BP), diabetes, obesity, smoking, and lack of physical activity, as well as poor adherence to evidence-based medication. This pragmatic, open-label proof-of-concept study conducted at three secondary care hospitals will randomly assign patients hospitalized with an ASCVD event to either: (i) brief advice, tailored discharge information to general practitioners, and a nurse-led outpatient visit (control), or (ii) the same interventions as (i) plus a single in-hospital motivational counselling session and access to a digital platform for a 6 months period with patient information/videos and an individualized treatment plan and follow-up plan. The primary end point will be between-group differences in the proportion who report having attended follow-up visits in primary (primary care physicians and community-based healthy life centres) and specialist (cardiac rehabilitation programs, hospital outpatient visits) healthcare after 8 weeks and 6 months follow-up. Secondary end points will be change in the SMART2 risk score and cardiovascular risk factors between baseline and 6 and 12 months follow-up. Exploratory end points will be changes in adherence to cardiovascular drugs, self-care behaviour, health literacy, patient activation, and quality of life.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion criteria (all the following): * Aged \>=18 years and signed informed consent and expected cooperation according to ICH/GCP and national/local regulations * Hospitalised with an planned or unplanned ASCVD event and/or established atherosclerosis * Access to a smartphone or tablet Exclusion criteria (any of the following): -Any condition or situation, that in the investigator's opinion could put the subject at significant risk, confound the study results, interfere significantly with the subject participation in the study, or rendering informed consent unfeasible not limited to: cognitive impairment, seizure disorders, active suicidal intent or plans, substance or alcohol dependence, psychotic disease, major depressive disorders or bipolar disorders, receiving concurrent psychological treatments, and ongoing night shift work. * Short life expectancy (\<12 months) due to end-organ (i.e COPD 4, CKD 4/5) or malignant diseases * Clinically significant symptoms of anxiety and depression (HADS A and/or HADS-D score ≥8) * Not being able to understand Norwegian.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Vestre Viken Trust Drammen hospital Drammen Buskerud Recruiting

More Vestre Viken Hospital Trust trials in Norway

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06738381 on ClinicalTrials.gov ↗ ← All trials in Norway