SMARTHEART Validation Study

University of Leicester

Status: Unknown

Conditions: Cardiovascular Diseases

Study type: Observational

Funder types: Other

Identifiers

NCT04755582

0693

Details and patient eligibility

About

To compare the accuracy of novel smartphone or wearable ECG devices to a gold standard ECG in patients with normal and abnormal ECGs.

Full description

Assess the effect of the following on the accuracy of the recorded ECG compared to a gold standard ECG:

• Posture or position of the patient
• Movement
• Amount of hair on the ECG site
• Skin condition (tone/dryness) Ability to detect a paced rhythm accurately A qualitative assessment of ECG devices, including the amount of artefact in the signal and ease of use of the device

Enrollment: 128 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Participant is willing and able to give informed consent for participation in the study.
• Must have an adequate understanding of written and spoken English
• Able (in the Investigators opinion) and willing to comply with study requirements.
• Must be over 18 years of age
• Must be deemed clinically stable by their direct care team.

Exclusion criteria

• Subjects who do not have an adequate understanding of written and spoken English
• Patients who are medically unstable, as defined by the patient's direct care team.
• Patients who are unable to give informed consent
• Patients who are deemed clinically unstable by their direct care team