Continuous data for better studies
Clinical research needs data from real life - not just from controlled study environments. Use the SaniQ OS telemedicine platform to continuously collect high-quality real-world data from the everyday lives of your test subjects.

3 Challenges in clinical studies:
3 Challenges in clinical studies:
Continuously generate high-quality data
Reduce the dropout rate
Communicate efficiently
How SaniQ supports you:
What used to be recorded as isolated data points in sterile practice rooms becomes a vivid picture of the course of symptoms in everyday life with SaniQ.
This is how SaniQ accompanies your test subjects through everyday life:
1. In the morning, they measure their vital signs at home using sensors connected to SaniQ.
2. At lunchtime, they answer digital questionnaires about their symptoms via the SaniQ patient app.
3. In the evening, they document how the new therapy affects their quality of life.
SaniQ transforms every day of study participation into valuable real-world data that you can track in real time via the SaniQ Dashboard.
SaniQ makes study participation much more convenient for test subjects:
They measure their vital signs from the comfort of their own home, answer digital questionnaires (PREMs & PROMs) when it suits them and receive gentle reminders via the patient app if they forget something. Should any questions arise, they can communicate immediately via the platform via chat or video consultation instead of waiting for the next appointment.
This flexibility means that significantly fewer participants terminate the study prematurely and the data quality increases noticeably due to more consistent participation.
Make treatment decisions when they are needed:
SaniQ notifies you directly when a test subject sends abnormal values. With just a few clicks, you can then view the current vital signs, evaluate questionnaire data and discuss the next steps via chat or video consultation without the patient first having to make an appointment or travel to the centre.
This ability to react quickly makes it possible to adapt the therapy efficiently and precisely to the course of symptoms, while at the same time ensuring complete documentation for the study data.
1. continuous data
This is how you accompany test subjects through their everyday life with SaniQ:
- In the morning, they measure their vital signs at home using sensors connected to SaniQ.
- At lunchtime, they answer digital questionnaires about their symptoms via the SaniQ patient app.
- In the evening, they document how the new therapy affects their quality of life.
SaniQ transforms every day of study participation into valuable real-world data that you can track in real time via the SaniQ Dashboard.
What used to be recorded as isolated data points in sterile practice rooms becomes a vivid picture of the course of symptoms in everyday life.

2. better compliance
SaniQ makes study participation much more convenient for test subjects:
They measure their vital signs from the comfort of their own home, answer digital questionnaires (PREMs & PROMs) when it suits them and receive gentle reminders via the patient app if they forget something. Should any questions arise, they can communicate immediately via the platform via chat or video consultation instead of waiting for the next appointment.
This flexibility means that significantly fewer participants terminate the study prematurely and the data quality increases noticeably due to more consistent participation.

3. more efficient therapy control
Make treatment decisions when they are needed:
SaniQ notifies you directly when a test subject sends abnormal values. With just a few clicks, you can then view the current vital signs, evaluate questionnaire data and discuss the next steps via chat or video consultation without the patient first having to make an appointment or travel to the centre.
This ability to react quickly makes it possible to adapt the therapy efficiently and precisely to the course of symptoms and at the same time ensure complete documentation for the study data.

- CE-approved Class I medical device
- GDPR-compliant data protection and ISO 27001-certified
- Standardised interfaces to your HIS (HL7, FHIR)
-
CE-approved
Class I medical device -
GDPR-compliant data protection
and certified according to ISO 27001 -
Standardised interfaces
to your HIS (HL7, FHIR)
Use Case: Telementor-COPD-Studie
Die durch den G-BA-Innovationsfonds geförderte Telementor-COPD-Studie untersucht den Nutzen von Telemedizin bei Patienten mit COPD.
Period: 2022-2025
Partner: Lungenclinic Großhansdorf, Astra Zeneca, Universitätsklinikum Schleswig-Holstein, Universitätsklinikum Hamburg-Eppendorg, u.v.m.
Number of participants in the study: 640
Content: Die Telementor-COPD-Studie ist eine durch den G-BA-Innovationsfonds geförderte, multizentrische, randomisierte und kontrollierte klinische Studie unter Konsortialführung der LungenClinic Großhansdorf. Gegenstand der Studie ist die Vermeidung von Exazerbationen bei COPD-Patient:innen durch digitale Prävention und häusliches Monitoring.
Link zur Studien-Website: https://www.telementor-copd.de/
Im Rahmen der Studie werden verschiedene Vitalwerte der Patienten mithilfe von SaniQ OS und angebundener Sensorik (Telespirometer, Smartwatch) monitoriert und durch das Studienpersonal ausgewertet:
- Telemonitoring der Lungenfunktion (FEV1), der Herz- und Atemfrequenz, der Blut-Sauerstoff-Sättigung sowie der täglichen Schrittzahl zur kontinuierlichen Patientenüberwachung
- API connection to the hospital information system for automated and bidirectional transmission of patient-related data
- Patient app zur aktiven Einbindung der Patienten in das Versorgungsprogramm und zum Generieren von Patient-Reported-Outcomes
- das Studienpersonal führt regelmäßige Televisits mit den angebundenen Patienten durch
Remote Patient Monitoring for COPD
When will telemonitoring for COPD become an integral part of standard care? Initial studies were promising - now a study project funded by the G-BA is set to provide clarity. In this article, we shed light on the current state of research and show what a sensible implementation could look like. ... Read more
Studies with SaniQ OS
SaniQ has already been used profitably in numerous clinical studies and research projects:

Telemonitoring for COPD in standard care?
Telementor-COPD is a multicentre, randomised and controlled clinical study funded by the Federal Joint Committee and led by LungenClinic Großhansdorf. With the help of SaniQ, it is investigating the benefits of telemonitoring for patients with COPD.

Telemedicine closes care gap
A team of doctors at Berlin's Charité hospital is breaking new ground to provide much-needed support to those affected by a neurological disease.
What researchers say about SaniQ



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