UMIC Validation Study

NCT ID: NCT01708577

Last Updated: 2012-11-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2011-07-31

Study Completion Date

2012-05-31

Brief Summary

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The purpose of the study is to evaluate the feasibility of a new wearable computerised system designed for an ongoing monitoring of sportsmen under real-life conditions. This system consists of different sensors and Bluetooth Transmitters interconnected by wires and integrated in the textile of a T-shirt. Several physiologic parameters including bioimpedance should be investigated under conditions relevant for an intensive physical activity, like high body temperature or partial dehydration. This system has to be tested under laboratory and "natural/open air" conditions, the obtained evaluations compared with standardised established diagnostic methods.

Detailed Description

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The new wearable sensor- and monitoring system has to be tested on 20 healthy sportsmen of both genders in the age between 18 and 35 years. The aim of the present study is the characterisation of technical parameters, diagnostic precision and practical applicability of this system, which should be able to measure and translate information of actual physiologic state during the physical activity of sportsmen under real-life conditions.

IPANEMA (Integrated Posture and Activity Network) is a construct consisting of electrodes and several specialized sensors integrated in the textile tissue of a T-Shirt and interconnected with "electronic nods", an equipment supporting the central computerized control system with information via Bluetooth signals.

This body sensor network enables ablations of electrical activity of heart (ECG), Bioimpedance Spectroscopy (BIS), measuring of temperature and humidity on the surface of skin, breathing intensity and acceleration of body movement.

The study is divided in 3 parts, the indoor part, the outdoor part, and the part of measurements under controlled artificial temperature conditions (climate chamber).

The outdoor measurements will be performed at different running tracks, e.g. at the Hochschulsportzentrum, Lousberg, and can be separated in two subtypes, the training and the competition.

The indoor study phase lasts ca. 2 hours, where the volunteers will be analysed during running on a tread mill with both, the IPANEMA system and common medical monitoring procedures. The evaluations of identical physiological parameters obtained by use of stationary diagnostic equipment, the ergospirometric device PowerCube Ergo, BIS measurement system Xitron Hydra 4200, infra-red camera VarioCam®hr-basic and standard medical ECG measurements are used as reference values. Two hours before the start and during the entire training phase, the experimental group is restricted to food and liquid intake in opposite to control group. These experimental conditions purpose to clarify several physiological effects of dehydration during sportive activities. The outdoor- and climate chamber- investigations do not prescribe the liquid deprivation.

The climate chamber measurements will be performed in a temperature controlled room. This measurement session can last up to 3 hours and temperature inside of climate chamber can be increased until 40Cº. Such conditions may simulate body sensor network and elicit physiological effects comparable to effects obtained during sportive activities. No sport is performed by volunteers during the climate chamber phase.

Conditions

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Healthy

Keywords

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heart rate sweating respiration acceleration of body movement heart activity.

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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IPANEMA validation without water intake

The one group is restricted to the water intake during the Indoor phase during testing the IPANEMA measurement system. The other group is not restricted to the water intake.

Group Type EXPERIMENTAL

Validation of the IPANEMA - measurement system

Intervention Type DEVICE

Control of the body conditions under real life conditions during a sportive activity.

IPANEMA validation with water intake

The one group is restricted to the water intake during the Indoor phase, the other group is not restricted to the water intake.

Group Type EXPERIMENTAL

Validation of the IPANEMA - measurement system

Intervention Type DEVICE

Control of the body conditions under real life conditions during a sportive activity.

Interventions

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Validation of the IPANEMA - measurement system

Control of the body conditions under real life conditions during a sportive activity.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* healthy, sporty person
* age 18-35 years
* able to give informed consent

Exclusion Criteria

* electrophobics
* metallic and / or electric implants
* balance difficulties
* cardiac insufficiency
* arterial hypotension
* truncal ataxia
* underage persons
* pregnancy
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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RWTH Aachen University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Stefan Krüger, Univ.-Prof.

Role: PRINCIPAL_INVESTIGATOR

Internal Medicine I, University Hospital Aachen

Locations

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Internal Medicine I, University Hospital

Aachen, North Rhine-Westphalia, Germany

Site Status

Countries

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Germany

Other Identifiers

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EK 180/11

Identifier Type: OTHER

Identifier Source: secondary_id

11-111

Identifier Type: -

Identifier Source: org_study_id