Feasibility of a Physiological Monitoring for Teleassistance to Isolated Workers in Industrial Cleaning

University Hospital, Angers

Overview

The purpose of the study is to test the feasibility of the monitoring of physiological parameters during operations of industrial cleaning

A letter about TIGER study is sent to employees eligible to participate. For volunteers, a written consent is signed after complete oral and written explanation of the protocol is signed. On the day of the industrial cleaning task, the employee wears the connected t-shirt and performs the cleaning. Data are retrieved on a 5 min interval basis. Physiological parameters above or beyond pre-defined limits are transmitted as potential alarms to an operational teleassistance center. A missing data (Invalid recording) are considered alarms. The number and causes of alarms are determined after the end of the cleaning task.

Study Type

INTERVENTIONAL

Allocation

Purpose

DEVICE_FEASIBILITY

Masking

NONE

Conditions

Work-Related Condition

Interventions

Connected T-shirtDEVICE

Ware of a connected T-shirt

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Employee involved in industrial cleaning task of non-ATEX sites (EXplosive ATmosphere) * Affiliation to the French National healthcare system * French speaking employee Exclusion Criteria: * Contraindication to the measures or procedures provided for in the study (physical characteristics do not allow measurements to be taken, wounds, etc.) * Pregnancy * Inability to understand the study goal * Employee protected by decision of law

Locations (1)

CHU

Angers, France

Outcomes

Primary Outcomes

Feasibility of T-shirt recording

Percentage of valid data from connected T-Shirt. The physiological data is fed back to an integrator and values for respiratory rate (FR), heart rate (HR), temperature (T °) and activity index are calculated over a period of 5 minutes. These values are only calculated if 15% of the raw data can be used over each period of 5 minutes.

Time frame: 12 months

Secondary Outcomes

Percentage of alarms processed in less than 3 minutes

Number of alarms processed in less than 3 minutes

Time frame: 12 months

Data from ClinicalTrials.gov

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