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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02114749
Other study ID # University Hospital, Grenoble
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 24, 2014
Est. completion date December 13, 2017

Study information

Verified date May 2018
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is aimed to develop analysis methods and measurements tools for physiological variables : respiration, circulation and their mutual interactions and with the functions involved in the daily life in healthy volunteers (drinking, eating, sleeping, coughing...). The devices that are used are non invasive. The development of these tools needs to be validated on physiological signals obtained in healthy volunteers.


Description:

The analysis and interpretation of a record consist, for example, to measure the amplitude of the respiratory modulation of the cardiac period, a witness of the level of the subject's sympathetic activity.

To do this, a mathematical model of this oscillation is adjusted on the experimental data, and its characteristics (amplitude, phase, non-linearity...) are considered indexes of the interaction to be compared with the same characteristics in other conditions.

The transition to clinical applications requires validation of the developed tools on physiological signals recorded on healthy volunteers in a non-clinical environment, avoiding extra psychological stress in the Protocol followed.

Whether it is for the development of tools or their validation, it is essential that the sensors used are non-invasive.

Recorded situations are those of everyday life, such as working (only sedentary work are envisaged), eat, talk, rest and move from one place of life to another one.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date December 13, 2017
Est. primary completion date December 13, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- healthy, major and socially insured human subjects

Exclusion Criteria:

- deprived of liberty, hospitalized and protected human subjects

Study Design


Related Conditions & MeSH terms


Intervention

Device:
a set of wearable respiration and cardiac monitoring devices
feasibility of methods for detecting physiological state changes from a set of wearable respiration and cardiac monitoring devices

Locations

Country Name City State
France University Hospital Grenoble
France TIMC - pavillon Taillefer - CHU GRENOBLE cedex 9

Sponsors (3)

Lead Sponsor Collaborator
University Hospital, Grenoble Centre National de la Recherche Scientifique, France, Université Joseph Fourier

Country where clinical trial is conducted

France, 

References & Publications (5)

Ben Lamine S, Calabrese P, Perrault H, Dinh TP, Eberhard A, Benchetrit G. Individual differences in respiratory sinus arrhythmia. Am J Physiol Heart Circ Physiol. 2004 Jun;286(6):H2305-12. Epub 2004 Jan 29. — View Citation

Eberhard A, Calabrese P, Baconnier P, Benchetrit G. Comparison between the respiratory inductance plethysmography signal derivative and the airflow signal. Adv Exp Med Biol. 2001;499:489-94. — View Citation

Emeriaud G, Eberhard A, Benchetrit G, Debillon T, Baconnier P. Calibration of respiratory inductance plethysmograph in preterm infants with different respiratory conditions. Pediatr Pulmonol. 2008 Nov;43(11):1135-1141. doi: 10.1002/ppul.20923. — View Citation

Fiamma MN, Straus C, Thibault S, Wysocki M, Baconnier P, Similowski T. Effects of hypercapnia and hypocapnia on ventilatory variability and the chaotic dynamics of ventilatory flow in humans. Am J Physiol Regul Integr Comp Physiol. 2007 May;292(5):R1985-93. Epub 2007 Jan 11. — View Citation

Fontecave-Jallon, Gumery P-Y, Calabrese P, Briot R, Baconnier P. A wearable technology revisited for cardio-respiratory functional exploration : Stroke volume estimation form respiratory inductive plethysmography. International journal of eHealth and Medical Communications, 4, 2013

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility and use of developed methods and tools in clinical or fundamental research protocols or in systems for physiological monitoring in humans The new tools for identification and monitoring of the physiological state of a subject will be developed from a set of non-invasive measures at rest. Resulting physiological state identification will then be validated on registrations on the same subjects in different daily life circumstances. up to 24 months
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