MOTIONPOD (TM) Validation and Calibration Study

Not Applicable

Completed

• Conditions: Energy Expenditure
• Interventions: Device: MOTIONPOD (TM) measures

• Registration Number: NCT01317732
• Lead Sponsor: Hospices Civils de Lyon

Brief Summary

In this study we propose 1) to develop a new multisensor monitoring system associating a tri-axial accelerometer and a magnetometer to measure physical activity in free-living adults, 2) to perform its calibration and assess its validity in a series of activity tasks in comparison with the measure of energy expenditure by indirect calorimetry as the criterion measure, and with existing physical activity monitors (cardiofrequencemetry and accelerometers used either alone or in combination). Briefly the subjects will perform a series of standardized activity tasks of different intensities and a 30-min free physical activity period while wearing 6 MOTIONPOD(TM) and different commercial activity monitors. Physical activity energy expenditure will be measured using a metabolic gas analyser.

Data of the 30 first subjects will be used to develop new algorithms to identify the different activity tasks and to estimate the related energy expenditures. Data of the following 30 subjects will be used to validate the MotionPOD(TM) against indirect calorimetry and existing physical activity monitors

Detailed Description

Not available

Study Timeline

• Study Start: 2010-10
• Study First Submitted: 2011-03-16
• Study First Submitted QC: 2011-03-16
• Study First Posted: 2011-03-17
• Primary Completion: 2013-10
• Study Completion: 2013-10
• Status Verified: 2014-03
• Last Update Submitted: 2019-05-23
• Last Update Posted: 2019-05-28

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Normal-weight, overweight or obesity according to body mass index
• Low,moderate or high level of physical activity as estimated by questionnaire
• No angina and/or peripheral arterial disease symptoms or medical history

Exclusion Criteria

• Subjects with cardiac implants
• Claustrophobic subjects
• Drug use that could affect energy expenditure
• Medical history or evolving disease which are a contra-indication for moderate physical exercise

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
MOTIONPOD (TM)	MOTIONPOD (TM) measures	-

Primary Outcome Measures

Name	Time	Method
Estimation by the MOTIONPODTM of the physical activity energy expenditure (PAEE) during a 30-min free activity period in comparison with the measure of PAEE by indirect calorimetry	30 minutes

Secondary Outcome Measures

Name	Time	Method
Estimation by the MOTIONPODTM of the physical activity energy expenditure during each of the tasks performed during the experiment in comparison with 1) indirect calorimetry, 2) existing commercially activity monitors	During three hours
Intensity classification by the MOTIONPODTM of the physical activity energy expenditure during each of the tasks performed during the experiment and during the 30-min free activity period.	During three hours	Intensity classification by the MOTIONPODTM of the physical activity energy expenditure during each of the tasks performed during the experiment and during the 30-min free activity period in comparison with 1) indirect calorimetry, 2) existing commercially activity monitors
Identification and classification of the tasks performed during a 30-min free activity period	30 minutes

Trial Locations

Locations (1)

Hospices Civils de Lyon Centre de Recherche en Nutrition Humaine Rhône-Alpes (CRNH-RA); 🇫🇷 Pierre Bénite, France