Skip to main content
OpenTrials
Completed

NCT Number: NCT02348554

A Smartphone Application to Evaluate Energy Expenditure and Duration of Activities for Overweight and Obese People

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre de Recherche en Nutrition Humaine d'Auvergne

Clermont-Ferrand, 63000, France

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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
  • subject willing to comply with study procedures
  • affiliated to National Health Insurance

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
  • refusal to be registered on the national volunteers data file
  • currently participating or who having got 4500€ in this year before to have participated in another clinical trial

Treatment and study plan

Controlled conditions

Behavioral

The 13 volunteers in controlled conditions performed each of the nine activities several times according to the activity scenario: sitting, slow, normal and brisk walking, climbing and descending stairs (eight floors), standing, slow running and taking public transportation (tramway). The duration of each activity varied from 2 to 20 minutes.

Free-living conditions

Behavioral

The spontaneous activities of 30 volunteers were recorded in the free-living conditions for a full day selected either during the week or the weekend.

Primary outcomes

  1. Accelerometry

    Time frame: 1 day

    Measures acquired by smartphones including a tri-axial accelerometer

Secondary outcomes

  1. Energy expenditure

    Time frame: 1 day

    Sensor: Fitmate

  2. Energy expenditure

    Time frame: 1 day

    Sensor: Armband

  3. Energy expenditure

    Time frame: 1 day

    Sensor: Actiheart

Other outcomes

  1. Rest energy expenditure

    Time frame: 1 day

    Measurement of rest energy expenditure under canopy by Fitmate

  2. Rest energy expenditure

    Time frame: 1 day

    Measurement of rest energy expenditure by using Armband

  3. Rest energy expenditure

    Time frame: 1 day

    Measurement of rest energy expenditure by using Actiheart

Sponsors and collaborators

Lead sponsor

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

Other

Collaborators

  • Almerys

Registry information

Official study title

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

Acronym: eMouve3

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Jan 28, 2015
Registry last updated
Jan 28, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.