Stroke Clinical Trial
— MOTI-strokeOfficial title:
Characterizing the Neural Bases of Motivational Disorders After Stroke
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.
| Status | Recruiting |
| Enrollment | 90 |
| Est. completion date | January 2023 |
| Est. primary completion date | January 2023 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | 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 |
| Country | Name | City | State |
|---|---|---|---|
| France | Urgences cérébro-vasculaires hopital Pitié-Salpêtrière | Paris |
| Lead Sponsor | Collaborator |
|---|---|
| Institut National de la Santé Et de la Recherche Médicale, France |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Reward sensitivity | The reward sensitivity measures the impact of reward values on behavior | 1 day | |
| Primary | Effort sensitivity | The effort sensitivity measures the impact of effort costs on behavior | 1 day |
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