Impact of Enhanced Information on Subjective Information Level and PROMs in Patients with Aortic Stenosis

ConditionAortic Stenosis Disease

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18+

SponsorHeart and Diabetes Center North-Rhine Westfalia

About this trial

The aim of this trial is to evaluate if an enhanced information by using a mobile App can increase subjective information level in patients with severe aortic stenosis and may therefore improve patient-reported outcomes.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

severe aortic valve stenosis

planned aortic valve replacement (TAVI)

Patient is willing and able to complete the surveys in German language

Written informed consent by the trial subject

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

Application of App
Device
Full Access to Mobile App

Treatment groups

250 Participants

are divided into 2 treatment groups

Group A: Full access to a mobile AppExperimental treatment 1 intervention

Group B: Restricted access to a mobile AppOther 1 intervention

Trial outcomes

Primary outcomes

Subjective information level (EORTC QOL-INFO 25 questionnaire)

Time frame

From enrollment to the end of FU at 3 months

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Heart and Diabetes Center North-Rhine Westfalia

Lead sponsor

Source ClinicalTrials.gov

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