A Smartphone Application to Evaluate Energy Expenditure and Duration of Activities in Free-living Conditions (eMouve2)
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT01995162 |
Recruitment Status :
Completed
First Posted : November 26, 2013
Last Update Posted : November 26, 2013
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
The Focus of the Study Was to Estimate Energy Expenditure Thanks to Accelerometry Data Collected by a Smartphone. | Device: Energy expenditure estimation | Not Applicable |
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.
Thus, the proposed EE estimation function has been created using accelerometry data collected from 10 volunteers equipped with a smartphone and two research sensors (Armband and Actiheart) used to estimate EE during several controlled activities. The research sensors' data serves as reference during the creation and evaluation of the proposed function.
It has been evaluated with data of 6 other volunteers in free-living conditions in the previous eMouve project.
eMouve2 consists in acquiring more data from 24 new volunteers in order to validate the function in free-living conditions.
This EE estimation function using the smartphone technology is dedicated to light- and moderate-intensity activities, and we believe it can be a new way to help people controlling their daily physical activity level.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 24 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Prevention |
Official Title: | A Smartphone Application to Evaluate Energy Expenditure and Duration of Moderate-intensity Activities in Free-living Conditions (eMouve 2) |
Study Start Date : | April 2013 |
Actual Primary Completion Date : | June 2013 |
Actual Study Completion Date : | October 2013 |
Arm | Intervention/treatment |
---|---|
Experimental: Free-living conditions |
Device: Energy expenditure estimation
Volunteers were asked to wear sensors during about 12 hours, one day. They wore 2 research sensors that estimate energy expenditure: Armband and Actiheart. They also wore a smartphone (in a front pant pocket) that collected accelerometry data. |
- Accelerometry [ Time Frame: about 17Hz (duration: about 12 hours) ]Measures acquired by a smartphone (it contains several sensors, including a tri-axial accelerometer)
- Energy expenditure [ Time Frame: one point recorded each minute for about 12 hours ]Sensor: Armband
- Energy expenditure [ Time Frame: one point recorded each minute for about 12 hours ]Sensor: Actiheart

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years to 60 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- men and women
- age: 18-60 years
- BMI between 18.5 and 25 kg/m²
- subject considered as healthy after clinical examination and medical questionnaire
- women of childbearing age: use of a contraceptive method
- subject with normal rest electrocardiogram (validated by a cardiologist)
- 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
- 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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01995162
France | |
Centre de Recherche en Nutrition Humaine Auvergne | |
Clermont Ferrand, France, 63000 |
Responsible Party: | Martine DUCLOS, PUPH, University Hospital, Clermont-Ferrand |
ClinicalTrials.gov Identifier: | NCT01995162 |
Other Study ID Numbers: |
AU1028 2013-A00188-37 ( Other Identifier: ANSM ) |
First Posted: | November 26, 2013 Key Record Dates |
Last Update Posted: | November 26, 2013 |
Last Verified: | November 2013 |