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Not yet recruiting NCT07677735

Non-contact Patient Monitoring With Millimeter Wave Radar Technology.

No phase Interventional Radar Monitoring Physiologic Monitoring

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: monitoring physiological and movement-based data.
Who it may be relevant to
Registry conditions: Radar, Monitoring, Physiologic Monitoring. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Development of a Contactless Patient Monitoring System Using Millimeter Wave Radar Technology

Overview

This study aims to develop a millimeter wave radar technology-based patient monitoring system that allows for the monitoring of physiological and movement-based data in healthcare settings without requiring physical contact with individuals. The study will involve the creation of hardware and software components for processing, analyzing, and converting signals obtained through radar sensors into clinically meaningful data.

Interventions

  • Device monitoring physiological and movement-based data
    monitoring physiological and movement-based data

Primary outcome measures

  • Data collection with the prototype device. [Time frame: 3 months]

Eligibility criteria

Inclusion criteria

  • Participating in the research as a researcher

Exclusion criteria

  • Wanting to withdraw from the research

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07677735 · 55754-1 TUSEB

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗