Development of a Torso Patch Sensor (C-TraQ) as a Companion Device to a Fingertip Sensor (TipTraQ) for Direct Monitoring of Respiratory Effort
Development and Validation of Chest Patch Sensor for Physiological Signal Measurement and Sleep Apnea Evaluation
1 other identifier
observational
180
1 country
1
Brief Summary
The existing PranaQ system utilizes a fingertip sensor that captures PPG(Photoplethysmography) and accelerometer data, and its clinical validation is well-established. While PPG alone has shown effectiveness in diagnosing obstructive sleep apnea, its limited data channels restrict comprehensive evaluation. For instance, it struggles to link apnea events with body position or differentiate between central and obstructive sleep apnea. To address these limitations, the PranaQ system incorporates new sensors, specifically the chest patch sensor, to monitor respiratory movements via accelerometer signals. The additional respiration signal has the potential to improve diagnostic accuracy for apnea through additional information from respiratory effort.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 5, 2026
CompletedFirst Submitted
Initial submission to the registry
July 29, 2026
CompletedFirst Posted
Study publicly available on registry
August 4, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 23, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 23, 2027
August 4, 2026
July 1, 2026
10 months
July 29, 2026
July 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Respiratory Rate
PSG recording estimated respiratory rate as ground truth to compare with the C-TraQ-generated respiratory rate.
one night
Sleep Position
Sleep Position measured by PSG as ground truth to compare with C-TraQ generated sleep position
One night
AHI
Technician labeled AHI based on PSG signal to compare with PranaQ system's prediction.
One night
Eligibility Criteria
Patient who is scheduled for a sleep study.
You may qualify if:
- Subjects must be 18 years of age or older.
You may not qualify if:
- Opioids use
- Chronic Obstructive Lung Disease, Global Initiative for Chronic Obstructive
- Lung Disease (GOLD) categorization 3 or 4
- Devastating strokes, with a modified Rankin score (mRS) ≥ 4
- Interstitial lung disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- PranaQ Pte. Ltd.lead
Study Sites (1)
Taipei Veterans General Hospital
Taipei, Taiwan, 201, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 29, 2026
First Posted
August 4, 2026
Study Start
June 5, 2026
Primary Completion (Estimated)
March 23, 2027
Study Completion (Estimated)
March 23, 2027
Last Updated
August 4, 2026
Record last verified: 2026-07