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Characterizing the Neural Bases of Motivational Disorders After Stroke (MOTI-stroke)

Primary Purpose

Stroke

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Motivation tests
Sponsored by
Institut National de la Santé Et de la Recherche Médicale, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Stroke

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria (healthy volunteers):

  • Right-handed
  • Age > 18 years old
  • Able to squeeze a hand-grip
  • Signature of consent form
  • Affiliation to an Health Insurance Scheme or beneficiary of such a scheme

Inclusion Criteria (patients):

  • Age > 18 years old
  • Able to squeeze a hand-grip
  • Signature of consent form
  • Affiliation to an Health Insurance Scheme or beneficiary of such a scheme
  • Stroke of the medial frontal lobe and not affecting the lateral frontal lobe OR stroke of the lateral frontal lobe and not affecting the medial frontal lobe

Exclusion Criteria (healthy volunteers):

  • Under justice protection
  • History of neurological or psychiatric diseases
  • Evolving disease that could impede volunteer participation during the whole study
  • Ongoing psychotropic drug or stopped for less than 3 weeks
  • Treatment that could interfer with subject performance
  • Chronical use of illicit psychoactive drugs or the day of the exam
  • Pregnant, parturient or breastfeeding woman
  • Exclusion period of another research
  • Contra-indication to MRI scan
  • Comprehension difficulties or difficulties to perform the study cognitive tests

Exclusion Criteria (patients):

  • Under justice protection
  • Evolving disease that could impede volunteer participation during the whole study
  • Chronical use of illicit psychoactive drugs or the day of the exam
  • Pregnant, parturient or breastfeeding woman
  • Exclusion period of another research
  • Contra-indication to MRI scan
  • Comprehension difficulties or difficulties to perform the study cognitive tests
  • Brain sequela with important cognitive deficiencies preventing cognitive test interpretation according to the investigator

Sites / Locations

  • Urgences cérébro-vasculaires hopital Pitié-SalpêtrièreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Other

Other

Other

Arm Label

medial frontal stroke

lateral frontal stroke

Healthy participants

Arm Description

20 patients (up to 10 patients can be replaced) with a stroke in the medial frontal lobe will be included in this arm, and will undergo motivation phenotyping.

20 patients (up to 10 patients can be replaced) with a stroke in the lateral frontal lobe will be included in this arm, and will undergo motivation phenotyping.

20 healthy participants (up to 10 healthy participants can be replaced) will be included in this arm, and will undergo motivation phenotyping.

Outcomes

Primary Outcome Measures

Reward sensitivity
The reward sensitivity measures the impact of reward values on behavior
Effort sensitivity
The effort sensitivity measures the impact of effort costs on behavior

Secondary Outcome Measures

Full Information

First Posted
November 8, 2018
Last Updated
June 28, 2021
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT03741140
Brief Title
Characterizing the Neural Bases of Motivational Disorders After Stroke
Acronym
MOTI-stroke
Official Title
Characterizing the Neural Bases of Motivational Disorders After Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
October 22, 2020 (Actual)
Primary Completion Date
January 2023 (Anticipated)
Study Completion Date
January 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to quantify elementary mechanisms of motivation, with innovative tools adapted to clinical settings, in healthy subjects, and in stroke patients, and to investigate their predictive value related to morbimortality, disability, and dependence. The secondary aim of the study is to investigate the neural substrates of motivational mechanisms, and to study the impact of lesions in the grey and the white matter, the influence of lesion site, and the consequences of disconnection in functional networks.
Detailed Description
Disorders of motivation, such as apathy, are among the most prevalent symptoms in neuropsychiatric disorders and during chronic diseases. They have a major impact on patients' physical activity and lifestyle, and on their involvement in their own care. They affect a wide range of morbidity outcomes, alter functional recovery in rehabilitation, impair long-term disability, and prevent patients from returning to an active and independent life. Yet, the neural bases of motivational deficits remain largely unknown. Current diagnostic tools are sparse and cannot distinguish between distinct mechanisms responsible for apathetic syndromes. Besides, current treatments remain extremely limited. However, recent advances in the field of neuroeconomics - the science of decision-making - have provided concept and tools to study the neurobiological bases of elementary cognitive processes underlying motivated behaviors. These theories suggest that the brain implements optimization processes that determine our behaviors by minimizing the cost of our actions while maximizing their expected benefits. The adaptation of tools developed for basic research now enables the assessment of these cognitive mechanisms. Elementary deficits of motivation will be assessed with a phenotyping battery of motivation tests in 20 healthy subjects (up to 10 healthy subjects can be replaced), 20 patients (up to 10 patients can be replaced) with a stroke in the medial prefrontal cortex, and 20 patients (up to 10 patients can be replaced) with a stroke in the insula. This battery will allow us to characterize, at the patient's level, elementary processes such as the encoding and the learning rate of goal values or effort costs, the modulation of value with delay or episodic context, the modulation of cost with fatigue, and the resolution of cost-benefit trade-offs. We will record morbimortality outcomes, such as functional recovery, disability, quality of life and burden for caregivers. Symptom-Lesion mapping studies and voxel-based morphometry studies will be performed using whole brain MRI measures of structural and functional integrity.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
medial frontal stroke
Arm Type
Other
Arm Description
20 patients (up to 10 patients can be replaced) with a stroke in the medial frontal lobe will be included in this arm, and will undergo motivation phenotyping.
Arm Title
lateral frontal stroke
Arm Type
Other
Arm Description
20 patients (up to 10 patients can be replaced) with a stroke in the lateral frontal lobe will be included in this arm, and will undergo motivation phenotyping.
Arm Title
Healthy participants
Arm Type
Other
Arm Description
20 healthy participants (up to 10 healthy participants can be replaced) will be included in this arm, and will undergo motivation phenotyping.
Intervention Type
Diagnostic Test
Intervention Name(s)
Motivation tests
Intervention Description
Motivation tests will characterize elementary deficits of motivation
Primary Outcome Measure Information:
Title
Reward sensitivity
Description
The reward sensitivity measures the impact of reward values on behavior
Time Frame
1 day
Title
Effort sensitivity
Description
The effort sensitivity measures the impact of effort costs on behavior
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria (healthy volunteers): Right-handed Age > 18 years old Able to squeeze a hand-grip Signature of consent form Affiliation to an Health Insurance Scheme or beneficiary of such a scheme Inclusion Criteria (patients): Age > 18 years old Able to squeeze a hand-grip Signature of consent form Affiliation to an Health Insurance Scheme or beneficiary of such a scheme Stroke of the medial frontal lobe and not affecting the lateral frontal lobe OR stroke of the lateral frontal lobe and not affecting the medial frontal lobe Exclusion Criteria (healthy volunteers): Under justice protection History of neurological or psychiatric diseases Evolving disease that could impede volunteer participation during the whole study Ongoing psychotropic drug or stopped for less than 3 weeks Treatment that could interfer with subject performance Chronical use of illicit psychoactive drugs or the day of the exam Pregnant, parturient or breastfeeding woman Exclusion period of another research Contra-indication to MRI scan Comprehension difficulties or difficulties to perform the study cognitive tests Exclusion Criteria (patients): Under justice protection Evolving disease that could impede volunteer participation during the whole study Chronical use of illicit psychoactive drugs or the day of the exam Pregnant, parturient or breastfeeding woman Exclusion period of another research Contra-indication to MRI scan Comprehension difficulties or difficulties to perform the study cognitive tests Brain sequela with important cognitive deficiencies preventing cognitive test interpretation according to the investigator
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raphael Le Bouc, PD, PhD
Phone
+33 (0) 1 42 16 18 54
Ext
+33
Email
raphael.lebouc@icm-institute.org
Facility Information:
Facility Name
Urgences cérébro-vasculaires hopital Pitié-Salpêtrière
City
Paris
ZIP/Postal Code
75013
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raphael Le Bouc
Phone
+33 (0)1 42 16 18 54
Email
raphael.lebouc@icm-institute.org

12. IPD Sharing Statement

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Characterizing the Neural Bases of Motivational Disorders After Stroke

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