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Clinical Trials/NCT02348554
NCT02348554
Completed
Not Applicable

A Smartphone Application to Evaluate Energy Expenditure and Duration of Activities in Free-living Conditions for Overweight and Obese People (eMouve3)

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
Enrollment
43
Locations
1
Primary Endpoint
Accelerometry
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The aim of this study was to validate functions for estimating energy expenditure in controlled and free-living conditions. This method was based on accelerometry data acquired from smartphones worn in a trouser pocket. The developed functions have been compared to the estimations provided by three research devices named Fitmate, Armband and Actiheart.

Detailed Description

There is a growing interest in evaluating physical activity and energy expenditure (EE) to provide feedback to the user. The use of mass-market sensors such as accelerometers offers a promising solution for the general public due to the growing smartphone market over the last decade. Two previous studies allowed to propose a function named PredEE, which has been tested on normal-weighted volunteers. This EE estimation function has been tested and improved with data collected from 43 overweight volunteers equipped with smartphones and two or three research sensors (Fitmate, Armband and Actiheart in controlled conditions, and Armband and Actiheart in free-living conditions). Research sensors' data serves as reference during the evaluation and improvement of the proposed function. This EE estimation function using the smartphone technology is dedicated to light- and moderate-intensity activities, and the investigators believe it can be a new way to help people controlling their daily physical activity level.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
August 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Martine DUCLOS

Physician

Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement

Eligibility Criteria

Inclusion Criteria

  • men and women
  • age: 18-60 years
  • BMI between 28 and 42 kg/m²
  • subject considered as healthy after clinical examination and medical questionnaire
  • no pregnant women
  • subject with normal rest electrocardiogram (validated by a cardiologist)
  • certificate of non-indication against the practice of exercise stress testing delivered by a physician
  • subject with normal blood pressure (\<140/90 mm Hg) with or without medical treatment
  • subject with no foot pad problem
  • subject giving his/her written informed consent

Exclusion Criteria

  • respiratory failure or cardiovascular problem
  • non-indication against the practice of exercise stress testing
  • known cardiac decompensation or myocardial infarction
  • surgery made less than 6 months before the study beginning
  • pregnant women and nursing mother
  • current infectious pathology
  • abnormal electrocardiogram
  • not affiliated to national health insurance people
  • under legal guardianship
  • refusal to sign informed consent

Outcomes

Primary Outcomes

Accelerometry

Time Frame: 1 day

Measures acquired by smartphones including a tri-axial accelerometer

Secondary Outcomes

  • Energy expenditure(1 day)

Study Sites (1)

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