The Box: using smart technology to improve one-year outcome of myocardial infarction patients

The Box: using smart technology to improve one-year outcome of myocardial infarction patients - The Box

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON43527

Enrollment

200

Registered

2016-05-10

Start date

2016-05-11

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

heart attack Myocardial infarction

Interventions

Patients will be randomized to either *The Box* or regular follow-up. Patients who have been randomized to The Box will receive a box containing a smartphone compatible ECG monitor, a weight scale,

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Myocardial infarction (either ST or NST elevation) 2. Patient is able to communicate in English or Dutch language 3. Patient is familiar with smartphone technology

Exclusion criteria

Exclusion criteria: 1. Body Mass Index > 35 kg•m-2 2. Patient is included in another randomized controlled trial 3. Patient is

Design outcomes

Primary

Measure	Time frame
The primary endpoint of the study will be the percentage of patients with controlled blood pressure in both groups.	—

Secondary

Measure	Time frame
• Scores of SFQ-questionnaires • Hospital-patient contact • Amount of hospital visits • Scores of Rand-36 questionnaires • Major Adverse Cardiac Events • Time between discharge from hospital and completion of device installation • Cost-effectiveness of interventions in both groups • Scores of medication-adherence questionnaires	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)