search
Back to results

Mobile App and Digital System for Patients After Myocardial Infarction (afterAMI)

Primary Purpose

mHealth, Telemedicine

Status
Unknown status
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Mobile application (afterAMI)
Sponsored by
Medical University of Warsaw
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for mHealth focused on measuring Myocardial infarction, Telemedicine, Mobile health

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • 1st Department of Cariology of Medcial University of WarsawRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard care

Mobile app care

Arm Description

Patients randomized to standard care arm will take part in the rehabilitation program according to regular schedule. Additionally every patient will have 2 cardiological visits: 1 and 6 months after the hospitalization due to MI.

Patients randomized to standard care arm will take part in the rehabilitation program according to regular schedule. Additionally every patient will have 2 cardiological visits: 1 and 6 months after the hospitalization due to MI. On top of that every patient will be given an access to mobile application, which will support rehab process. The application stands as a educational and coordination tool.

Outcomes

Primary Outcome Measures

Rehospitalization or urgent outpatient visit
The number and reasons of rehospitalizations and urgent outpatient visits.
Rehospitalization or urgent outpatient visit
The number and reasons of rehospitalizations and urgent outpatient visits.
Cardiovascular risk factors control - hypertension
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 - hypertension
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 mass
Body mass will be measured. Change [kg] from baseline body mass will be analyzed.
Cardiovascular risk factors control - body mass
Body mass will be measured. Change [kg] from baseline body mass will be analyzed.
Cardiovascular risk factors control - nicotinism
The number of patients who are active smokers will be assessed. The change from baseline will be analyzed.
Cardiovascular risk factors control - nicotinism
The number of patients who are active smokers will be assessed. The change from baseline will be analyzed.
Cardiovascular risk factors control - dyslipidemia
LDL cholesterol level will be measured and the change from baseline will be analyzed.
Cardiovascular risk factors control - dyslipidemia
LDL cholesterol level will be measured and the change from baseline will be analyzed.

Secondary Outcome Measures

Quality of life - MacNew
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 - MacNew
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 state
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
Quality of life - descriptive profile of a respondent's health state
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 assessment
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 Applied to me to some degree, or some of the time - SOMETIMES Applied to me to a considerable degree, or a good part of time - OFTEN 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.
DASS 21 - Depression, anxiety and stress assessment
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 Applied to me to some degree, or some of the time - SOMETIMES Applied to me to a considerable degree, or a good part of time - OFTEN 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. Higher result in every section contributes to higher severity in depression, anxiety and stress.
Cardiovascular risk factor knowledge
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.
Cardiovascular risk factor knowledge
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 work
In case of patients who were previously working the amount of patients who came back to work will be assessed.
Return to work
In case of patients who were previously working the amount of patients who came back to work will be assessed.

Full Information

First Posted
February 4, 2021
Last Updated
March 8, 2021
Sponsor
Medical University of Warsaw
search

1. Study Identification

Unique Protocol Identification Number
NCT04793425
Brief Title
Mobile App and Digital System for Patients After Myocardial Infarction
Acronym
afterAMI
Official Title
The Impact of Mobile Application and a Digital Support System on the Prevention of Cardiovascular Events in Patients After a Myocardial Infarction.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Unknown status
Study Start Date
December 1, 2020 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Warsaw

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
mHealth, Telemedicine
Keywords
Myocardial infarction, Telemedicine, Mobile health

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard care
Arm Type
No Intervention
Arm Description
Patients randomized to standard care arm will take part in the rehabilitation program according to regular schedule. Additionally every patient will have 2 cardiological visits: 1 and 6 months after the hospitalization due to MI.
Arm Title
Mobile app care
Arm Type
Experimental
Arm Description
Patients randomized to standard care arm will take part in the rehabilitation program according to regular schedule. Additionally every patient will have 2 cardiological visits: 1 and 6 months after the hospitalization due to MI. On top of that every patient will be given an access to mobile application, which will support rehab process. The application stands as a educational and coordination tool.
Intervention Type
Behavioral
Intervention Name(s)
Mobile application (afterAMI)
Intervention Description
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.
Primary Outcome Measure Information:
Title
Rehospitalization or urgent outpatient visit
Description
The number and reasons of rehospitalizations and urgent outpatient visits.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Rehospitalization or urgent outpatient visit
Description
The number and reasons of rehospitalizations and urgent outpatient visits.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Cardiovascular risk factors control - hypertension
Description
Systolic and diastolic blood pressure values will be analyzed with special focus on meeting the values recommended by European Society of Cardiology guidelines.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Cardiovascular risk factors control - hypertension
Description
Systolic and diastolic blood pressure values will be analyzed with special focus on meeting the values recommended by European Society of Cardiology guidelines.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Cardiovascular risk factors control - body mass
Description
Body mass will be measured. Change [kg] from baseline body mass will be analyzed.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Cardiovascular risk factors control - body mass
Description
Body mass will be measured. Change [kg] from baseline body mass will be analyzed.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Cardiovascular risk factors control - nicotinism
Description
The number of patients who are active smokers will be assessed. The change from baseline will be analyzed.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Cardiovascular risk factors control - nicotinism
Description
The number of patients who are active smokers will be assessed. The change from baseline will be analyzed.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Cardiovascular risk factors control - dyslipidemia
Description
LDL cholesterol level will be measured and the change from baseline will be analyzed.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Cardiovascular risk factors control - dyslipidemia
Description
LDL cholesterol level will be measured and the change from baseline will be analyzed.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Secondary Outcome Measure Information:
Title
Quality of life - MacNew
Description
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.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Quality of life - MacNew
Description
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.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Quality of life - descriptive profile of a respondent's health state
Description
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
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Quality of life - descriptive profile of a respondent's health state
Description
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
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
DASS 21 - Depression, anxiety and stress assessment
Description
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 Applied to me to some degree, or some of the time - SOMETIMES Applied to me to a considerable degree, or a good part of time - OFTEN 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.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
DASS 21 - Depression, anxiety and stress assessment
Description
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 Applied to me to some degree, or some of the time - SOMETIMES Applied to me to a considerable degree, or a good part of time - OFTEN 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. Higher result in every section contributes to higher severity in depression, anxiety and stress.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Cardiovascular risk factor knowledge
Description
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.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Cardiovascular risk factor knowledge
Description
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.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.
Title
Return to work
Description
In case of patients who were previously working the amount of patients who came back to work will be assessed.
Time Frame
This outcome will be assessed 1 month after discharge from the hospital.
Title
Return to work
Description
In case of patients who were previously working the amount of patients who came back to work will be assessed.
Time Frame
This outcome will be assessed 6 months after discharge from the hospital.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bartosz Krzowski, MD
Phone
+48 791347820
Email
bartosz.krzowski@wum.edu.pl
Facility Information:
Facility Name
1st Department of Cariology of Medcial University of Warsaw
City
Warsaw
State/Province
Mazowieckie
ZIP/Postal Code
02-097
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bartosz Krzowski, MD
Phone
791347280
Ext
0048
Email
bartosz.krzowski@wum.edu.pl
First Name & Middle Initial & Last Name & Degree
Michał Peller, PhD
First Name & Middle Initial & Last Name & Degree
Łukasz Kołtowski, PhD
First Name & Middle Initial & Last Name & Degree
Paweł Balsam, PhD
First Name & Middle Initial & Last Name & Degree
Marcin D Grabowski, PhD
First Name & Middle Initial & Last Name & Degree
Bartosz Krzowski, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35729626
Citation
Krzowski B, Peller M, Boszko M, Hoffman P, Zurawska N, Jaruga K, Skoczylas K, Osak G, Koltowski L, Grabowski M, Opolski G, Balsam P. Mobile app and digital system for patients after myocardial infarction (afterAMI): study protocol for a randomized controlled trial. Trials. 2022 Jun 21;23(1):522. doi: 10.1186/s13063-022-06463-x.
Results Reference
derived

Learn more about this trial

Mobile App and Digital System for Patients After Myocardial Infarction

We'll reach out to this number within 24 hrs