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Clinical Trials/NCT01317732
NCT01317732
Completed
Not Applicable

Calibration and Validation of MOTIONPOD(TM) for Physical Activity Evaluation in Free-living Adults

Hospices Civils de Lyon1 site in 1 country60 target enrollmentOctober 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Energy Expenditure
Sponsor
Hospices Civils de Lyon
Enrollment
60
Locations
1
Primary Endpoint
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
Status
Completed
Last Updated
6 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
October 2013
Last Updated
6 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

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

Time Frame: 30 minutes

Secondary Outcomes

  • 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)
  • Identification and classification of the tasks performed during a 30-min free activity period(30 minutes)

Study Sites (1)

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