Study of Sensorimotor Compatibility Effects in Bipolar Affective Disorder.
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT03249857|
Recruitment Status : Recruiting
First Posted : August 15, 2017
Last Update Posted : September 30, 2019
|Condition or disease||Intervention/treatment||Phase|
|Bipolar Affective Disorder||Behavioral: cognitive tasks + IQ + MINI Behavioral: cognitive tasks||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||40 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Primary Purpose:||Basic Science|
|Official Title:||Study of Sensorimotor Compatibility Effects in Bipolar Affective Disorder.|
|Actual Study Start Date :||October 26, 2017|
|Estimated Primary Completion Date :||August 2020|
|Estimated Study Completion Date :||August 2020|
Patients suffering bipolar affective disorders and who will perform cognitive tasks + IQ + MINI + experimental task
Behavioral: cognitive tasks + IQ + MINI
Patients will perform different tasks:
Active Comparator: control group
Healthy volunteers (Control group) who will perform cognitive tasks + experimental task
Behavioral: cognitive tasks
Healthy volunteers will perform only the cognitive tasks = reaction time alert TEA, Zimmermann and Fimm, 2005 + Edinburgh laterality questionnaire (Oldfield, 1971) + experimental task (approach/ avoidance and affordance task).
- response time for avoidance and affordance task [ Time Frame: Months 24 ]Comparison of response time for avoidance and affordance task between patients and healthy volunteers.
- response time for affordance task [ Time Frame: Months 24 ]Comparison of response time for affordance task between patients and healthy volunteers.
- correlations with age at onset of the disease, the number of thymic decompensations and the existence of psychotic symptoms [ Time Frame: Months 24 ]These informations were collected of the medical file.
- response time and cognitive tests [ Time Frame: Months 24 ]Correlation between response time and cognitive tests of patients and healthy volunteers.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03249857
|Contact: Anne GROSSELIN, neuropychologue||(33)firstname.lastname@example.org|
|Contact: Anne GROSSELIN, email@example.com|
|St Etienne, France, 42055|
|Contact: Catherine MASSOUBRE, MD (0)477127962 ext +33 firstname.lastname@example.org|
|Principal Investigator: Catherine MASSOUBRE, MD PhD|
|Sub-Investigator: Marie-Christine OUVRY, MD|
|Sub-Investigator: Nathalie VIALLON, MD|
|Sub-Investigator: Stephane BOYER, MD|
|Sub-Investigator: Aurélia GAY, MD|
|Principal Investigator:||Catherine MASSOUBRE, MD PhD||CHU SAINT-ETIENNE|