NCT07677735

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
6

participants targeted

Target at below P25 for not_applicable

Timeline
2mo left

Started Aug 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 18, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

July 1, 2026

Completed
1 month until next milestone

Study Start

First participant enrolled

August 1, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

July 1, 2026

Status Verified

June 1, 2026

Enrollment Period

1 month

First QC Date

June 18, 2026

Last Update Submit

June 25, 2026

Conditions

RadarMonitoringPhysiologic Monitoring

Outcome Measures

Primary Outcomes (1)

  • Data collection with the prototype device.

    The developed prototype device will collect respiratory rate, heart rate, blood pressure, and cardiac output data from six healthy individuals acting as researchers.

    3 months

Study Arms (1)

Data collection with the prototype device.

OTHER

The developed prototype device will collect respiratory rate, heart rate, blood pressure, and cardiac output data from six healthy individuals acting as researchers.

Device: monitoring physiological and movement-based data

Interventions

monitoring physiological and movement-based dataDEVICE

monitoring physiological and movement-based data

Data collection with the prototype device.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Participating in the research as a researcher

You may not qualify if:

  • Wanting to withdraw from the research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Monitoring, Physiologic

Intervention Hierarchy (Ancestors)

Diagnostic Techniques and ProceduresDiagnosis

Central Study Contacts

RUKİYE KOKKIZ, LECTURER

CONTACT

+90 507 140 68 98rky_kokkiz@hotmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

June 18, 2026

First Posted

July 1, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

October 1, 2026

Last Updated

July 1, 2026

Record last verified: 2026-06