Completed

ActiGPSAssessment of Human Locomotion and Energy Expenditure Using Global Positioning Satellite and Accelerometry

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What is being collected

Data Collection

Collected from today forward - Prospective
Other
Who is being recruted

Over 18 Years
+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: February 2013
See protocol details

Summary

Principal SponsorUniversity Hospital, Angers
Last updated: November 6, 2019
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 2013

Actual date on which the first participant was enrolled.

The assessment of the physical activity (PA) and the energy expenditure (EE) is very important to estimate the morbi-mortality. However, each of these tools has its advantages and disadvantages but none of them provides a measure of all components dimensions that characterize the associated PA and EE. The current scientific prospects for measurement of PA tend to associate several measuring devices. To date, these perspectives are facilitated by technological developments and miniaturization of various devices. Thus, the purpose of the study is to evaluate wether GPS associated with accelerometer are able to assess the humain locomotion and energy expenditure during exercises.

NCT01805219
Principal SponsorUniversity Hospital, Angers
Last updated: November 6, 2019
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

67 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

5 inclusion criteria required to participate
Able to understand the protocol of the study
Informed consent of the participant
No exercise limitation
Older than 18
Show More Criteria
2 exclusion criteria prevent from participating
No informed consent of the participant
pregnant woman

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

University Hospital

Angers, FranceOpen University Hospital in Google Maps
CompletedOne Study Center