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Mobile App and Digital System for Patients After Myocardial Infarction

The Impact of Mobile Application and a Digital Support System on the Prevention of Cardiovascular Events in Patients After a Myocardial Infarction.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04793425
Acronym
afterAMI
Enrollment
100
Registered
2021-03-11
Start date
2020-12-01
Completion date
2023-07-31
Last updated
2021-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

mHealth, Telemedicine

Keywords

Myocardial infarction, Telemedicine, Mobile health

Brief summary

The treatment of acute myocardial infarction (MI) in Poland is at the level of standardized European care. However, the first months after MI are crucial from the perspective of patient's prognosis. It is extremely important to take care of all cardiovascular risk factors. Mobile application (afterAMI) supported by web system is a novel telemedical tool created to support patient and physician during the process of cardiac rehabilitation. The application has educational model with focus on cardiovascular risk factors and lifestyle after MI. Moreover, there is a module to control vital signs like blood pressure, heart rate, weight and many others. Additionally, application will send reminders for better drug adherence. 100 patients will be recruited to take part in the study. All of which will be hospitalized at the 1st Department and Clinic of Cardiology because of the MI. The aim of the project is to study the impact of application-supported model of care with comparison to standard care. At the end of the study cardiovascular risk factors control will be analysed, as well as rehospitalizations, patient's knowledge regarding risk factors, return to work and quality of life. This will be a prospective, open-label, randomized, single-centre study. All 100 patients will be observed 6 months after discharge from the hospital. End points will be assessed during control visit 1- and 6-months after inclusion into the study. This project is an example of a telemedicine solution application into everyday practice, which is consistent with multiple international cardiac societies.

Interventions

BEHAVIORALMobile application (afterAMI)

The rehabilitation process of the patients in the intervention group will be supported by the mobile application (afterAMI) with synchronized, dedicated web page. Patients in the intervention group will be given an access to educational data regarding their individualized diseases. Additionally every patient will receive regularly messages with notifications regarding lifestyle and adherence to the therapy. All reported vital signs (blood pressure, heart rate, weight and many more) will be analyzed every day and in case of need a short message will be sent to the patient with indication to go to the primary healthcare clinic/hospital. Additionally, application will send notifications with reminders to take drugs.

Sponsors

Medical University of Warsaw
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* signing the informed consent to participate in the study * hospitalization due to myocardial infarction * a mobile device with Internet access and the Android/iOS operating system * age \>17 years old * positive results of the test verifying the basic skills of using mobile applications

Design outcomes

Primary

MeasureTime frameDescription
Cardiovascular risk factors control - dyslipidemiaThis outcome will be assessed 1 month after discharge from the hospital.LDL cholesterol level will be measured and the change from baseline will be analyzed.
Rehospitalization or urgent outpatient visitThis outcome will be assessed 1 month after discharge from the hospital.The number and reasons of rehospitalizations and urgent outpatient visits.
Cardiovascular risk factors control - hypertensionThis outcome will be assessed 1 month after discharge from the hospital.Systolic and diastolic blood pressure values will be analyzed with special focus on meeting the values recommended by European Society of Cardiology guidelines.
Cardiovascular risk factors control - body massThis outcome will be assessed 1 month after discharge from the hospital.Body mass will be measured. Change \[kg\] from baseline body mass will be analyzed.
Cardiovascular risk factors control - nicotinismThis outcome will be assessed 1 month after discharge from the hospital.The number of patients who are active smokers will be assessed. The change from baseline will be analyzed.

Secondary

MeasureTime frameDescription
Quality of life - MacNewThis outcome will be assessed 1 month after discharge from the hospital.Quality of life will be assessed with MacNew questionnaire.Scoring of the MacNew is straight-forward. The maximum possible score in any domain is 7 \[high quality\] and the minimum is 1 \[poor quality\]. The quality of life is assessed with regard to physical, emotional and social aspect, as well as general quality of life. There are 27 questions in total.
Quality of life - descriptive profile of a respondent's health stateThis outcome will be assessed 1 month after discharge from the hospital.Quality of life will be assessed with EQ-5D-5L questionnaire. The 5-level EQ-5D version (EQ-5D-5L) was introduced by the EuroQol Group. There are 5 aspects examined: mobility, self-care, usual activity, pain/discomfort, anxiety/depression. Every part is assessed based on 5 level scale: LEVEL 1: indicating no problem LEVEL 2: indicating slight problems LEVEL 3: indicating moderate problems LEVEL 4: indicating severe problems LEVEL 5: indicating unable to/extreme problems
DASS 21 - Depression, anxiety and stress assessmentThis outcome will be assessed 1 month after discharge from the hospital.Depression, anxiety and stress assessment will be assessed with DASS 21 (Depression Anxiety Stress Scales) scale The DASS is a quantitative measure of distress along the 3 axes of depression, anxiety and stress. There are 21 questions, each has 4 possible answers: 0 Did not apply to me at all - NEVER 1. Applied to me to some degree, or some of the time - SOMETIMES 2. Applied to me to a considerable degree, or a good part of time - OFTEN 3. Applied to me very much, or most of the time - ALMOST ALWAYS There are 7 questions assigned to every aspect: depression, anxiety and stress respectively. Higher result in every section contributes to higher severity in depression, anxiety and stress.
Cardiovascular risk factor knowledgeThis outcome will be assessed 1 month after discharge from the hospital.Cardiovascular risk factor knowledge will be assessed with previously prepared questionnaire (10 questions). There are 9 single choice questions. Every correct answer is rewarded with a point. There is 1 open question, where the patient is asked to list known cardiovascular risk factors. Patient gets 1 point fo 1-2 CV risk factors, 2 points for 3-4 CV risk factors, 3 points for 5-6 CV risk factors and 4 points for \>6 named CV risk factors. The maximum score is 13 points , which indicates good cardiovascular risk factors knowledge. The minimum score is 0 points, which indicates poor cardiovascular risk factors knowledge.
Return to workThis outcome will be assessed 1 month after discharge from the hospital.In case of patients who were previously working the amount of patients who came back to work will be assessed.

Countries

Poland

Contacts

Primary ContactBartosz Krzowski, MD
bartosz.krzowski@wum.edu.pl+48 791347820

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026