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Healthy VolunteersActiGPSNCT01805219

Global Positioning Satellite and Accelerometry to Assess Human Locomotion (ACTI GPS)

An observational study of Healthy Volunteers, run by University Hospital, Angers at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of the study is to validate the association of the GPS and accelerometer tools in order to assess the humain locomotion during exercises. The hypotheses are: 1. GPS and accelerometer together can assess the human locomotion 2. GPS and accelerometer together can assess the energy expenditure during exercises Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Healthy Volunteers
What is being tested?
GPS and accelerometer recording (s) during exercises
How many people
67 participants
Where
1 siteFrance
Study dates
1 Feb 2013to 8 Jun 2016
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Healthy subjects

Who may be able to join

  • Older than 18
  • Informed consent of the participant
  • Able to understand the protocol of the study
  • Register to the social health insurance
  • No exercise limitation

Who cannot join

  • No informed consent of the participant
  • pregnant woman

Trial locations and contacts

1 site in 1 country.

France1 site
  • University Hospital

    Angers, 49933

Other trials in France

About this study

Official title: Assessment of Human Locomotion and Energy Expenditure Using Global Positioning Satellite and Accelerometry

The aim of the study is to validate the association of the GPS and accelerometer tools in order to assess the humain locomotion during exercises.

The hypotheses are:

  1. GPS and accelerometer together can assess the human locomotion
  2. GPS and accelerometer together can assess the energy expenditure during exercises
Read the detailed description

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.

Being tested
GPS and accelerometer recording (s) during exercises

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GPS and accelerometer recording (s) during exercisesOther

Study groups in NCT01805219
Study groupRoleWhat they receive
healthy subjectsNot described
Receives: Other: GPS and accelerometer recording (s) during exercises

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Defining optimal analysis parameter to accurately detect walking from stopping periods

    Predefined walking protocols will be recorded and the subjects asked to follow recorded procedures.

    Detection performance of walking and resting bouts (expressed by the percentage accuracy in the detection of walking and resting bouts actually performed) for: i) GPS alone; ii) Accelerometer alone; iii) both GPS and accelerometer

    Measured: up to 1 week

Secondary outcomes (1)
  1. Defining optimal analysis parameter to accurately detect speed and distance of periods of walking

    Predefined walking protocols will be recorded and the subjects asked to follow recorded procedures at a defined walking pace.

    Accuracy of speed and distance estimations (expressed by the typical error of estimate and the coefficient of variation) from: i) GPS alone; ii) Accelerometer alone; iii) both GPS and accelerometer.

    Measured: up to 1 week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Mar 2013 (estimated)
  2. Study start1 Feb 2013
  3. Primary completion8 Jun 2016
  4. Study completion8 Jun 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
67 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01805219
Sponsor's protocol ID
2012-A01411-42
Acronym
ActiGPS
Status last verified
Nov 2019
First submitted
18 Feb 2013
Last updated
6 Nov 2019
Results posted
No
Data monitoring committee
Yes

Publications

  • de Mullenheim PY, Dumond R, Gernigon M, Mahe G, Lavenu A, Bickert S, Prioux J, Noury-Desvaux B, Le Faucheur A. Predicting metabolic rate during level and uphill outdoor walking using a low-cost GPS receiver. J Appl Physiol (1985). 2016 Aug 1;121(2):577-88. doi: 10.1152/japplphysiol.00224.2016. Epub 2016 Jul 8.

    PubMed 27402559

Questions about this trial

What is this clinical trial studying?

An observational study of Healthy Volunteers, run by University Hospital, Angers at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Nov 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Defining optimal analysis parameter to accurately detect walking from stopping periods (time frame: up to 1 week). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01805219, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2019.

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