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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03260582
Enrollment
150
Registered
2017-08-24
Start date
2016-04-30
Completion date
2019-06-30
Last updated
2019-10-25

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

Conditions

Myocardial Infarction

Keywords

cardiac rehabilitation, eHealth, smartphone application

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.

Interventions

OTHERLifePod®

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.

Sponsors

Lund University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 74 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in submaximal exercise capacity in watts (W)Change between first (2-4 weeks post-MI) and second (4-6 months post-MI) submaximal exercise test conducted at physiotherapist visitsSubmaximal 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

MeasureTime frameDescription
Change in healthy diet indexChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIThe 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 habitsFirst (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIWhether the patient is a non-smoker, prior smoker or current smoker (self-report)
Change in weightChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIWeight measured in kg
Change in BMIChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIWeight in kilograms (kg) divided by height in meters (m) square
Change in waist circumferenceChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIWaist circumference measured in cm
Change in systolic blood pressureChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MISystolic blood pressure measured after 5 minutes of rest in supine position (mmHg)
Change in diastolic blood pressureChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIDiastolic blood pressure measured after 5 minutes of rest in supine position (mmHg)
Change in total cholesterolChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIFasting plasma total cholesterol
Change in LDL cholesterolChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIFasting plasma LDL cholesterol (mmol/L)
Change in self-reported healthChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MISelf-reported Health is measured using the Visual Analogue Scale (0-100)
Change in triglyceridesChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIFasting plasma triglycerides (mmol/L)
Change in fasting plasma glucoseChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIFasting plasma glucose (mg/dL)
Change in hemoglobin A1cChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIWhole-blood hemoglobin A1c (mmol/mol) by International Federation of Clinical Chemistry (IFCC) standards
Changes in self-reported physical activityChange between baseline, first (2-4 weeks post-MI) and second (4-6 months post-MI) physiotherapist visits post-MISelf-reported physical activity, as measured by Haskell and Frändin & Grimby
UptakeSix monthsThe proportion of patients who log on to the patient interface at least once
AdherenceSix monthsThe proportion of patients registering data at least twice per week on a weekly basis throughout the intervention period
Number of contacts with the CR staff12-14 monthsNumber of telephone and physical contacts with the CR staff during the follow-up period
Incident cardiovascular events at one yearOne yearIncidence 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 yearsThree yearsIncidence of cardiovascular events at three years after the index event: hospitalization for a new MI, heart failure or stroke and cardiovascular death
Change in HDL cholesterolChange between baseline, first (6-8 weeks post-MI) and second (12-14 months post-MI) nurse visits post-MIFasting plasma HDL cholesterol (mmol/L)

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026