Actively Recruiting
Efficiency of the Medidux Smartphone App for Post-Discharge Management in Patients Treated in Acute Admission Unit: A Randomized Controlled Trial
Led by Mobile Health AG · Updated on 2025-10-03
417
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
M
Mobile Health AG
Lead Sponsor
P
Palleos Healthcare GmbH
Collaborating Sponsor
AI-Summary
What this Trial Is About
This trial focuses on adults aged 18 and older admitted to Acute Admission Units (AAU) with non-urgent health complaints such as coughing, back pain, or abdominal discomfort. It aims to evaluate whether using the medidux132 smartphone app after discharge can reduce the rates of readmissions, emergency hospitalizations, and consultations with other medical providers within 7 days. The study compares this app-based monitoring approach with standard post-discharge care to understand its impact on patient outcomes. Participants are randomly assigned to either the intervention arm, where they use the medidux132 app to record symptoms and vital signs daily for 7 days after discharge, or the control arm, which receives usual care without the app. The app provides prompts and guidance to help users manage their symptoms and decide if further medical attention is needed. Follow-up assessments occur at 7 and 28 days post-discharge for all participants to evaluate symptom changes and healthcare use. During the study, participants will complete symptom tracking and vital sign monitoring through the app if in the intervention group, and both groups will attend follow-up consultations at day 7 and day 28. Researchers will measure outcomes including readmission rates, emergency hospitalizations, consultations with medical providers, symptom severity, and app usability. The primary outcome is the incidence of these events within 7 days after initial admission, with additional monitoring up to 28 days to assess longer-term effects.
CONDITIONS
Brief Title
Efficiency of the "Medidux" Smartphone App for Demission Management in Patients Medicated in Acute Admission Unit (AAU)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed informed consent form
- Age 18 years or older
- Admission to the involved Acute Admission Unit (AAU)
- Main symptom is coughing, back pain, or abdominal discomfort
- Classified in Emergency Severity Index (ESI) triage groups 4 or 5
- German-speaking
- Owns a smartphone or mobile device with iOS or Android operating system
You will not qualify if you...
- Under 18 years old
- Compliance to study protocol is doubtful due to mental, physical, or personal reasons
- Insufficient knowledge of smartphone or mobile device use
- Currently using or planning to use another electronic symptom monitoring system during the trial
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 7 days post-discharge
Participants use the medidux smartphone application to log daily health data, including symptoms and vital signs, for 7 days following discharge from the Acute Admission Unit. The app provides automated prompts and guidance for self-management and remote symptom monitoring to reduce readmissions and emergency hospitalizations.
Daily logging of health data via the smartphone app
Duration - Up to 28 days post-discharge
Participants attend follow-up assessments to evaluate symptom progression and healthcare utilization after discharge.
2 visits (day 7 and day 28 post-discharge)
Trial Site Locations
Total: 1 location
1
Notfallzentrum See-Spital Horgen
Horgen, Canton of Zurich, Switzerland, 8810
Actively Recruiting
Research Team
A
Andreas Trojan, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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