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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02470143
Other study ID # PDEN-IFRE 02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2015
Est. completion date December 31, 2018

Study information

Verified date February 2019
Source Hasselt University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The pilot study will investigate the usability of a mobile cycling application in a cardiac patient population during a one month study period.

The application's effectiveness regarding ability to reduce fear and increase motivation to exercise will be assessed.


Description:

This pilot study investigates the use of a mobile cycling application for patients with a cardiac disease that was developed by the Expertise Centre for Digital Media of Hasselt University in collaboration with the Faculty of Medicine & Life Sciences of Hasselt University. During the pilot study, the use of the cycling application and its impact on fear and motivation of patients with a cardiac disease during the rehabilitation is studied. The cycling application will be used on a smartphone, in combination with a wrist-worn heart rate monitor.

During the study, the patients will use the cycling application for one month, in which they can make use of the cycling application each time they are cycling outdoor in their home environment. Through questionnaires and interviews, the patients' experiences with respect to fear and motivation will be collected. Furthermore, the usability of the cycling application is evaluated through these questionnaires and interviews.


Recruitment information / eligibility

Status Completed
Enrollment 75
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients with coronary artery disease for which they received a percutaneous coronary intervention, coronary artery bypass grafting or drugs only.

- 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 with a history of VF, sustained VT and/or supraventricular tachycardia during the last 6 months before enrollment.

- Patients who due to cognitive, neurological and/or musculoskeletal constraints are unable to ride a bicycle.

- Patients with a pacemaker.

- Non-Dutch speaking patients

- Patients who simultaneously participate in another study

Study Design


Intervention

Behavioral:
Bike application arm
The intervention patients will use the cycling application on a smartphone, in combination with a wrist-worn heart rate monitor. During the study, the patients will use the cycling application for one month, in which they can make use of the cycling application each time they are cycling outdoor in their home environment.

Locations

Country Name City State
Belgium Jessa Ziekenhuis Hasselt

Sponsors (2)

Lead Sponsor Collaborator
Hasselt University Jessa Hospital

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Impact on motivation up to week 4
Secondary Usability of the cycling application By means of a questionnaire and an interview, the participants are asked about the usability of the application. This information will give insights in parts of the application that could be improved considering the usability. Up to week 4
Secondary Impact on fear By means of a questionnaire and an interview, questions are asked about participants' motivation for a tour up to week 4
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