Actively Recruiting
Surrogating Physician-recorded SCORE2 Risk Calculator Inputs by Using Auxiliary Data
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-02-18
250
Participants Needed
1
Research Sites
79 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of the clinical trial is to assess whether the data collected from wearable devices can reduce the uncertainty in predicting the cardiovascular disease (CVD) risk in women aged 40-69 years in a situation where information about the blood pressure and blood lipids are unavailable. Participants will: * Complete a screening and baseline assessment, including blood sample collection and vital parameter measurement. * Wear a wearable device for one week. * Fill in a work and sleep journal. * Complete a last visit assessment.
CONDITIONS
Official Title
Surrogating Physician-recorded SCORE2 Risk Calculator Inputs by Using Auxiliary Data
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Fluency in German (written and oral).
- Ownership of a smartphone.
- Signing the informed consent form.
You will not qualify if you...
- Diagnosis of cardiovascular disease.
- Diagnosis of diabetes mellitus.
- Diagnosis of chronic kidney disease.
- Diagnosis of familial hypercholesterolemia.
- Incapable of providing informed consent.
- Current employment at the Section Gynecological Endocrinology and Reproductive Medicine of the Department for Obstetrics and Gynecology at the Inselspital Bern or any other professional relation to one of the study project leaders / investigators.
- Concurrent participation in a clinical intervention study.
- Inability to comply with the study procedures for any reason, including language comprehension, psychiatric illness, general inability to get to the study site.
- Participant's smartphone not compatible with Fitrockr.
- Technical inability of participant's smartphone to connect to the smartwatch.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Hospital of Bern, Department of Gynecological Endocrinology & Reproductive Medicine
Bern, Switzerland, 3010
Actively Recruiting
Research Team
P
Petra Stute, Prof.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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