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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05771142
Other study ID # Smart_t-shirt_2021
Secondary ID 156/2022/Disp/AO
Status Recruiting
Phase
First received
Last updated
Start date March 27, 2023
Est. completion date May 31, 2023

Study information

Verified date February 2023
Source University of Bologna
Contact Luca Neri
Phone +14432538858
Email luca.neri9@unibo.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Evaluation of an innovative smart t-shirt capable to monitor ECG signal and related parameters through the comparison with a Holter ECG and a smartwatch


Description:

The primary purpose of this study is to evaluate the biosignal (ECG) acquisition features of the smart t-shirt, developed by University of Bologna in collaboration with AccYouRate S.p.A., comparing it with a standard Holter ECG. Secondly, the study wants to compare the parameters related to ECG signal calculated by the smart t-shirt with those calculated by commercial smartwatches.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date May 31, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: 1. Subjects agree to participate in the study and having dated and signed the informed consent form, 2. Subjects who have the capability to communicate, to make themselves understood, and to comply with the study's requirements, 3. Male or female aged = 18 years and = 90 years old, 4. Subjects with Cardiac electrophysiological (heart rhythm) pathologies or under screening for the assessment of possible cardiac electrophysiological pathologies. Exclusion Criteria: 1. Subjects that for different reasons have difficulties to wear the sensorized t-shirt or the alternative sensorized chest band: Movement's impairments; Dermatological reaction to t-shirt fabric or materials, 2. Any medical or surgical condition that would limit the patient adhesion to the study protocol, 3. Severe obesity and sever underweight, 4. Subject that are not able to understand the scope of the study.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Smart t-shirt
24h ECG Monitoring with the smart t-shirt under study
ECG Holter
24h ECG Monitoring with ECG Holter
Smartwatch
24h ECG Monitoring with a smartwatch

Locations

Country Name City State
Italy Policlinico Sant'Orsola Malpighi - University of Bologna Bologna

Sponsors (2)

Lead Sponsor Collaborator
University of Bologna AccYouRate S.p.A.

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Electrocardiogram (ECG): Heart rate (beats per minute) Smart t-shirt and ECG Holter comparison 24 hours
Primary Electrocardiogram (ECG): RR interval (seconds) Smart t-shirt and ECG Holter comparison 24 hours
Primary Electrocardiogram (ECG): Qualitative distinction of P-waves, QRS-complexes, T-waves, and noise levels Smart t-shirt and ECG Holter comparison 24 hours
Secondary Electrocardiogram (ECG): Heart rate (beats per minute) Smart t-shirt and smartwatch comparison 24 hours
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