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

Sponsor
Institut National de la Santé Et de la Recherche Médicale, France (Other)
Overall Status
Completed
CT.gov ID
NCT02496312
Collaborator
(none)
14
1
2.8

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Evaluation of Apathy Close to Real Life Situation
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
14 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official 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.
Actual Study Start Date :
Jul 10, 2015
Actual Primary Completion Date :
Oct 2, 2015
Actual Study Completion Date :
Oct 2, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: ECOCAPTURE

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

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

Outcome Measures

Primary Outcome Measures

  1. Occurrence of each behavior from the ethogram [45 min]

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

  2. Frequency of each behavior from the ethogram [45 min]

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

  3. Duration of each behavior from the ethogram [45 mn]

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

  4. Number of different behaviors [45 mn]

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

  5. Activity classes [45 mn]

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

  6. Body positions [45 mn]

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

  7. Energy expenditure [45 mn]

    [Provided by the MOVE MOVISENS sensor] kcal.

  8. MET [45 mn]

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

  9. Steps [45 mn]

    [Provided by the MOVE MOVISENS sensor] Counting steps.

  10. Activity intensity [45 mn]

    [Provided by the MOVE MOVISENS sensor] g.

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

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

Investigators

  • Principal Investigator: Richard LEVY, PhD, MD, INSERM UMR_S 1127, ICM

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Institut National de la Santé Et de la Recherche Médicale, France
ClinicalTrials.gov Identifier:
NCT02496312
Other Study ID Numbers:
  • C15-14
  • 2015-A0087-42
First Posted:
Jul 14, 2015
Last Update Posted:
Nov 6, 2017
Last Verified:
Oct 1, 2017
Keywords provided by Institut National de la Santé Et de la Recherche Médicale, France
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 6, 2017