HeartHab, Can a Patient-tailored Application Support Coronary Artery Disease Patients During Rehabilitation?
NCT ID: NCT02668757
Last Updated: 2018-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2016-03-31
2017-12-31
Brief Summary
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Motivational aspects and usability data will be collected during study period by means of app logs and/or questionnaires/interviews.
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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HeartHab application arm
Patients in the HeartHab application arm will receive the mobile application during study period.
HeartHab application intervention
The intervention patients will use the HeartHab application on a smartphone. During the study, the patients will use the HeartHab application for 4-6 weeks.
Interventions
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HeartHab application intervention
The intervention patients will use the HeartHab application on a smartphone. During the study, the patients will use the HeartHab application for 4-6 weeks.
Eligibility Criteria
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Inclusion Criteria
* Patients that have completed the standard cardiac rehabilitation program
* Patients who have access to a computer and a WiFi internet connection
* Patients that are able to go to the rehabilitation centre ReGo of Jessa Hospital
* Patients who signed the informed consent document
Exclusion Criteria
* Patients who due to cognitive, neurological and/or musculoskeletal constraints are unable to ride a bicycle.
* Patients with a pacemaker or defibrillator.
* Non-Dutch speaking patients
* Patients who simultaneously participate in another study
18 Years
70 Years
ALL
No
Sponsors
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Hasselt University
OTHER
Responsible Party
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prof. dr. Paul Dendale
prof. dr.
Principal Investigators
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Locations
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Jessa Ziekenhuis
Hasselt, , Belgium
Countries
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Other Identifiers
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HeartHab-001
Identifier Type: -
Identifier Source: org_study_id
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