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Validation of Hyfe CoughMonitor in infants with bronchiolitis

Validation of Hyfe CoughMonitor in infants with bronchiolitis - HYF_01

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00032480
Enrollment
10
Registered
2023-10-17
Start date
2024-02-01
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infant bronchiolitis

Interventions

Group 1: Inpatient infants diagnosed with bronchiolitis whose cough frequency is recorded with the Hyfe CoughMonitor and an MP3 recorder over the course of one night.

Sponsors

ARCIM Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0 Months to 12 Months

Inclusion criteria

Inclusion criteria: 1. Hospital admission at the pediatric department of the Filderklinik. 2. Diagnosis of bronchiolitis. Diagnosis is clinical, based on the combination of respiratory distress (such as tachypnea, grunting, nasal flaring, retractions) and fine crackles sometimes accompanied by wheezing on auscultation. 3. Written parental consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Critically ill infants who have an immediate need for intensive care admission. 2. Insufficient German language skills of the parents to understand the written patient information.

Design outcomes

Primary

MeasureTime frame
Correlation between the hourly cough frequency recorded with the Hyfe CoughMonitor and the values calculated from the annotated continuous recordings.

Countries

Germany

Contacts

Public ContactJan Vagedes

ARCIM Institute

j.vagedes@arcim-institute.de+49 711 77031688

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026