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Completed

NCT Number: NCT02496312

Quantitative Evaluation of Apathy Close to Real Life Situation by Means of a Multimodal Sensor System Integrated.

The purpose of this study is to provide relevant quantitative evaluation of apathy close to real life situation by means of a multimodal sensor system integrated.

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Key information

About this study

The investigators try to measure the amount of goal-directed behaviour and to detect the pattern of apathy. The main objective of this pilot phase is to select the variables of goal-directed behaviour from the list of metrics providing by the multimodal acquisition system in healthy subjects and patients with frontotemporal dementia.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Diagnosis of Frontotemporal Dementia (FTD) according to diagnostic criteria reported by Rascovsky et al. (2011).
  • Understanding of the instructions and capacity to realize the cognitive tasks.
  • Capacity to read, to understand and to sign legal document of information
  • Capacity for informed consent for research, capacity to sign consent
  • MMSE score > 20
  • Absence of other cerebral pathology.
  • Absence of psychiatric disease interfering with the assessment of the tests
  • Absence of excessive psychotropic use
  • Access to National Healthcare Insurance
  • Accompanied with a caregiver

Exclusion criteria

  • Excessive psychotropic use
  • Incapacity or refusal to realize the experimental tasks
  • Subject deprived of freedom by an administrative or court order
  • Subject under legal protective measure.
  • Incapacity for informed consent for research
  • Participation in another biomedical research
  • Airway obstruction risk
  • Reduction of activity not attributable to another chronic pathological condition

Treatment and study plan

Evaluation of Apathy Close to Real Life Situation

Behavioral

Quantitative Evaluation of Apathy Close to Real Life Situation by Means of a Multimodal Sensor System Integrated.

Primary outcomes

  1. Occurrence of each behavior from the ethogram

    Time frame: 45 min

    [Provided by the video recording and The Observer NOLDUS software]

  2. Frequency of each behavior from the ethogram

    Time frame: 45 min

    [Provided by the video recording and The Observer NOLDUS software]

  3. Duration of each behavior from the ethogram

    Time frame: 45 mn

    [Provided by the video recording and The Observer NOLDUS software]

  4. Number of different behaviors

    Time frame: 45 mn

    [Provided by the video recording and The Observer NOLDUS software]

  5. Activity classes

    Time frame: 45 mn

    [Provided by the MOVE MOVISENS sensor] lying, sitting, ...

  6. Body positions

    Time frame: 45 mn

    [Provided by the MOVE MOVISENS sensor] lying left, ...

  7. Energy expenditure

    Time frame: 45 mn

    [Provided by the MOVE MOVISENS sensor] kcal.

  8. MET

    Time frame: 45 mn

    [Provided by the MOVE MOVISENS sensor] The Metabolic Equivalent of Task. MET level.

  9. Steps

    Time frame: 45 mn

    [Provided by the MOVE MOVISENS sensor] Counting steps.

  10. Activity intensity

    Time frame: 45 mn

    [Provided by the MOVE MOVISENS sensor] g.

Sponsors and collaborators

Lead sponsor

Institut National de la Santé Et de la Recherche Médicale, France

Other Gov

Registry information

Official study title

Quantitative Evaluation of Apathy Close to Real Life Situation by Means of a Multimodal Sensor System Integrated in Healthy Subjects and Patients With Frontotemporal Dementia. Pilot Phase.

Acronym: ECOCAPTURE

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Jul 14, 2015
Registry last updated
Jun 5, 2026

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.

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