Effect of Monitoring Continuous Glucose Levels and Physical Activity Via Wearables on Cardiovascular Risk Factors

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Basel, Switzerland

About this trial

The study aims to assess the effect of smart watches and continuous glucose measuring devices on cardiovascular risk factors.

Eligibility criteria

Qualifiers

Informed Consent signed by the subject

Completed outpatient cardiac rehabilitation

Diagnosis of coronary heart disease

Access to a smartphone for the duration of the study

Disqualifiers

Diseases which limit physical activity including angina with incomplete revascularisation, arrhythmogenic cardiomyopathy, stroke with residual disease, and major orthopaedic disorders

Known or suspected non-compliance

Inability to follow the procedures of the investigation, e.g., due to language problems, psychological disorders, dementia, etc. of the subject

Diabetic patients receiving insulin therapy

Trial design

Treatments tested in this trial

  • Fitbit Inspire 2
  • Abbott Freestyle Libre 3

Treatment groups

100 Participants
are divided into 2 treatment groups