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Implementation and Assessment of a Life-style Focused Patient Support Application in Myocardial Infarction Patients

Primary Purpose

Myocardial Infarction

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
LifePod®
Sponsored by
Lund University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myocardial Infarction focused on measuring cardiac rehabilitation, eHealth, smartphone application

Eligibility Criteria

18 Years - 74 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

  • Age < 75 years. This cut-off is set as only those < 75 years of age are followed in the national Secondary Prevention after Heart Intensive Care Admission (SEPHIA) registry
  • Has suffered an MI within the last 2 weeks
  • Owns a smartphone and/or has access to internet via a computer or surf pad and can handle the software

Exclusion criteria

  • Expected survival < 1 year
  • Dementia, severe psychiatric illness or drug abuse
  • Severe physical handicap limiting the patient´s ability to participate in exercise-based CR
  • Not able to speak or understand the Swedish language
  • Three-vessel disease requiring coronary artery bypass grafting

Sites / Locations

  • Dept of Cardiology, Skane University Hospital
  • Dept of Cardiology, Skane University Hospital
  • Dept of Cardiology

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control arm (n=50)

Intervention arm: LifePod arm (n=100)

Arm Description

Patients randomized to the control arm will receive usual cardiac rehabilitation care post-myocardial infarction.

In addition to usual cardiac rehabilitation care, patients randomized to the LifePod arm will receive access to the LifePod® support software for six months.

Outcomes

Primary Outcome Measures

Change in submaximal exercise capacity in watts (W)
Submaximal exercise capacity reflects the patients´ level of physical fitness.The submaximal exercise test is performed on a bicycle ergometer according to the World Health Organisation (WHO) protocol, with an increased workload of 25W every 4.5 minutes The initial starting load, 25W or 50W, is decided, based on the patient's exertion history. After two and four minutes of each workload; heart rate, rate of perceived exertion according to Borg's rating of perceived exertion scale (RPE) and subjective symptoms, including chest pain and dyspnea according to Borg's Category Ratio Scale, CR-10, scale are rated. After three minutes, the systolic blood pressure is registered. The exercise test is discontinued at Borg RPE 17 and/or dyspnea 7 on Borg's CR-10 scale.

Secondary Outcome Measures

Change in self-reported health
Self-reported Health is measured using the Visual Analogue Scale (0-100)
Change in healthy diet index
The healthy diet index is a four-item questionnaire used to evaluate dietary habits within the Swedish Secondary Prevention after Heart Intensive Care Admission (SEPHIA) registry
Smoking habits
Whether the patient is a non-smoker, prior smoker or current smoker (self-report)
Change in weight
Weight measured in kg
Change in BMI
Weight in kilograms (kg) divided by height in meters (m) square
Change in waist circumference
Waist circumference measured in cm
Change in systolic blood pressure
Systolic blood pressure measured after 5 minutes of rest in supine position (mmHg)
Change in diastolic blood pressure
Diastolic blood pressure measured after 5 minutes of rest in supine position (mmHg)
Change in total cholesterol
Fasting plasma total cholesterol
Change in LDL cholesterol
Fasting plasma LDL cholesterol (mmol/L)
Change in HDL cholesterol
Fasting plasma HDL cholesterol (mmol/L)
Change in triglycerides
Fasting plasma triglycerides (mmol/L)
Change in fasting plasma glucose
Fasting plasma glucose (mg/dL)
Change in hemoglobin A1c
Whole-blood hemoglobin A1c (mmol/mol) by International Federation of Clinical Chemistry (IFCC) standards
Changes in self-reported physical activity
Self-reported physical activity, as measured by Haskell and Frändin & Grimby
Uptake
The proportion of patients who log on to the patient interface at least once
Adherence
The proportion of patients registering data at least twice per week on a weekly basis throughout the intervention period
Number of contacts with the CR staff
Number of telephone and physical contacts with the CR staff during the follow-up period
Incident cardiovascular events at one year
Incidence of cardiovascular events at one year after the index event: hospitalization for a new MI, heart failure or stroke and cardiovascular death
Incident cardiovascular events at three years
Incidence of cardiovascular events at three years after the index event: hospitalization for a new MI, heart failure or stroke and cardiovascular death

Full Information

First Posted
June 14, 2017
Last Updated
October 24, 2019
Sponsor
Lund University
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1. Study Identification

Unique Protocol Identification Number
NCT03260582
Brief Title
Implementation and Assessment of a Life-style Focused Patient Support Application in Myocardial Infarction Patients
Official Title
Implementation and Assessment of a Life-style Focused Patient Support Application (App) and Activity Trackers for Improving Risk Factor Management, Physical Activity, Quality of Life and Prognosis in Post-myocardial Infarction Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
April 2016 (Actual)
Primary Completion Date
June 2019 (Actual)
Study Completion Date
June 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lund University

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 study will assess the efficacy of a web-based application as a complement to traditional exercise-based cardiac rehabilitation for improvement of secondary prevention outcomes in post-myocardial infarction patients, compared with usual care. The hypothesis is that the intervention enhances patient adherence to lifestyle advice (exercise training, daily physical activity, healthy diet and tobacco abstinence) and medication, resulting in better risk factor control and prognosis as well as increased self-rated health.
Detailed Description
It is well documented that participation in cardiac rehabilitation (CR) programs improves risk factor control and therapy adherence, enhances quality of life and reduces recurrent events. However, the current incomplete fulfilment of guideline recommended CR targets is a matter of concern. Also, while international recommendations advocate program flexibility and individual tailoring, most of the current CR programs are rigid, time-limited and demand substantial health care resources. Therefore, all main international heart associations have claimed for the reengineering of CR to enhance access, adherence, and effectiveness. The general call is for the development of innovative and cost-effective CR programs oriented to modify lifestyle and behaviour with sustainable results and that may be easily integrated in the pre-existing health care structures.eHealth i.e. the use of electronic communication and information technologies in health care, offers a whole new array of possibilities to provide clinical care. These include for example distance monitoring via telecommunication and sensors, interactive computer programs and smart phone applications. While there are thousands of available eHealth applications on the market, only a small minority have been tested in a controlled manner with proper guidance from health care personnel. The study will assess the efficacy of a web-based patient support application as a complement to traditional exercise-based CR for improvement of secondary prevention outcomes in post-MI patients, compared with usual care. The hypothesis is that the intervention enhances patient adherence to lifestyle advice (exercise training, daily physical activity, healthy diet and tobacco abstinence) and medication, resulting in better risk factor control and prognosis as well as increased self-rated health. A secondary hypothesis is that complementing the application with an activity tracker (accelerometer in a smart bracelet) will enhance the effect of the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Infarction
Keywords
cardiac rehabilitation, eHealth, smartphone application

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control arm (n=50)
Arm Type
No Intervention
Arm Description
Patients randomized to the control arm will receive usual cardiac rehabilitation care post-myocardial infarction.
Arm Title
Intervention arm: LifePod arm (n=100)
Arm Type
Experimental
Arm Description
In addition to usual cardiac rehabilitation care, patients randomized to the LifePod arm will receive access to the LifePod® support software for six months.
Intervention Type
Other
Intervention Name(s)
LifePod®
Intervention Description
The software is a web-based application designed to support persons adhering to lifestyle advice and medication. The patient can log information about lifestyle (i.e. diet, exercise, and smoking), measurements (i.e. weight, pulse and blood pressure), symptoms and medication and can review data in graphs displaying registered values in relation to recommended targets. The software provides positive feedback on healthy choices and gives general recommendations on exercise training, physical activity and healthy diet. Reminders are generated in the case of decreasing registrations. Finally, short text messages (SMS) will be sent out 2-3 times a week with tips on healthy lifestyle.
Primary Outcome Measure Information:
Title
Change in submaximal exercise capacity in watts (W)
Description
Submaximal exercise capacity reflects the patients´ level of physical fitness.The submaximal exercise test is performed on a bicycle ergometer according to the World Health Organisation (WHO) protocol, with an increased workload of 25W every 4.5 minutes The initial starting load, 25W or 50W, is decided, based on the patient's exertion history. After two and four minutes of each workload; heart rate, rate of perceived exertion according to Borg's rating of perceived exertion scale (RPE) and subjective symptoms, including chest pain and dyspnea according to Borg's Category Ratio Scale, CR-10, scale are rated. After three minutes, the systolic blood pressure is registered. The exercise test is discontinued at Borg RPE 17 and/or dyspnea 7 on Borg's CR-10 scale.
Time Frame
Change between first (2-4 weeks post-MI) and second (4-6 months post-MI) submaximal exercise test conducted at physiotherapist visits
Secondary Outcome Measure Information:
Title
Change in self-reported health
Description
Self-reported Health is measured using the Visual Analogue Scale (0-100)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in healthy diet index
Description
The healthy diet index is a four-item questionnaire used to evaluate dietary habits within the Swedish Secondary Prevention after Heart Intensive Care Admission (SEPHIA) registry
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Smoking habits
Description
Whether the patient is a non-smoker, prior smoker or current smoker (self-report)
Time Frame
First (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in weight
Description
Weight measured in kg
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in BMI
Description
Weight in kilograms (kg) divided by height in meters (m) square
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in waist circumference
Description
Waist circumference measured in cm
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in systolic blood pressure
Description
Systolic blood pressure measured after 5 minutes of rest in supine position (mmHg)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in diastolic blood pressure
Description
Diastolic blood pressure measured after 5 minutes of rest in supine position (mmHg)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in total cholesterol
Description
Fasting plasma total cholesterol
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in LDL cholesterol
Description
Fasting plasma LDL cholesterol (mmol/L)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in HDL cholesterol
Description
Fasting plasma HDL cholesterol (mmol/L)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in triglycerides
Description
Fasting plasma triglycerides (mmol/L)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in fasting plasma glucose
Description
Fasting plasma glucose (mg/dL)
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Change in hemoglobin A1c
Description
Whole-blood hemoglobin A1c (mmol/mol) by International Federation of Clinical Chemistry (IFCC) standards
Time Frame
Change between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MI
Title
Changes in self-reported physical activity
Description
Self-reported physical activity, as measured by Haskell and Frändin & Grimby
Time Frame
Change between baseline, first (2-4 weeks post-MI) and second (4-6 months post-MI) physiotherapist visits post-MI
Title
Uptake
Description
The proportion of patients who log on to the patient interface at least once
Time Frame
Six months
Title
Adherence
Description
The proportion of patients registering data at least twice per week on a weekly basis throughout the intervention period
Time Frame
Six months
Title
Number of contacts with the CR staff
Description
Number of telephone and physical contacts with the CR staff during the follow-up period
Time Frame
12-14 months
Title
Incident cardiovascular events at one year
Description
Incidence of cardiovascular events at one year after the index event: hospitalization for a new MI, heart failure or stroke and cardiovascular death
Time Frame
One year
Title
Incident cardiovascular events at three years
Description
Incidence of cardiovascular events at three years after the index event: hospitalization for a new MI, heart failure or stroke and cardiovascular death
Time Frame
Three years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Age < 75 years. This cut-off is set as only those < 75 years of age are followed in the national Secondary Prevention after Heart Intensive Care Admission (SEPHIA) registry Has suffered an MI within the last 2 weeks Owns a smartphone and/or has access to internet via a computer or surf pad and can handle the software Exclusion criteria Expected survival < 1 year Dementia, severe psychiatric illness or drug abuse Severe physical handicap limiting the patient´s ability to participate in exercise-based CR Not able to speak or understand the Swedish language Three-vessel disease requiring coronary artery bypass grafting
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margret Leosdottir, MD, PhD
Organizational Affiliation
Skane University Hospital and Lund University, Malmo, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dept of Cardiology, Skane University Hospital
City
Lund
ZIP/Postal Code
222 41
Country
Sweden
Facility Name
Dept of Cardiology, Skane University Hospital
City
Malmo
ZIP/Postal Code
20502
Country
Sweden
Facility Name
Dept of Cardiology
City
Umeå
ZIP/Postal Code
907 46
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35357316
Citation
Ogmundsdottir Michelsen H, Sjolin I, Back M, Gonzalez Garcia M, Olsson A, Sandberg C, Schiopu A, Leosdottir M. Effect of a Lifestyle-Focused Web-Based Application on Risk Factor Management in Patients Who Have Had a Myocardial Infarction: Randomized Controlled Trial. J Med Internet Res. 2022 Mar 31;24(3):e25224. doi: 10.2196/25224.
Results Reference
derived
PubMed Identifier
30678709
Citation
Gonzalez M, Sjolin I, Back M, Ogmundsdottir Michelsen H, Tanha T, Sandberg C, Schiopu A, Leosdottir M. Effect of a lifestyle-focused electronic patient support application for improving risk factor management, self-rated health, and prognosis in post-myocardial infarction patients: study protocol for a multi-center randomized controlled trial. Trials. 2019 Jan 24;20(1):76. doi: 10.1186/s13063-018-3118-1.
Results Reference
derived
Links:
URL
http://www.cross-solutions.com/
Description
Cross Technology Solutions home page

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Implementation and Assessment of a Life-style Focused Patient Support Application in Myocardial Infarction Patients

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