Mental Time Travel and Identity in Bipolar Disorder Patients
NCT ID: NCT02793518
Last Updated: 2016-06-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
60 participants
INTERVENTIONAL
2013-05-31
2016-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Social Cognition, Memory, and Executive Functions in Bipolar Disorder and Major Depressive Disorder
NCT06740331
A Trial of Functional Remediation in Patients With Bipolar Disorder
NCT04577508
Attentional Biases, Reward Sensitivity, and Cognitive Control in Adults With Bipolar Disorder
NCT03829787
Bipolarity - Depression in Children and Adolescent Suicide Attempters: Better Diagnosis to Prevent Recurrence
NCT03116503
Shared Medical Decision Making in the Prophylactic Treatment of Bipolar Disorder
NCT03245593
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* A group of 30 patients aged 18 to 60 years and followed in the psychiatry department of adult CHU Reims for bipolar disorder type I (DSM-IV criteria).
* A group of 30 control subjects with no personal or family history of severe psychiatric disorder (bipolar disorder, schizophrenia or schizoaffective disorder), recruited from the staff of the University Hospital of Reims, the medical faculty of Reims or Marnais center health promotion of Reims, via the intranet and paper display.
The two groups will be matched for age (± 3 years), sex and educational level (± 2 years).
Plan of investigation: the study will be done in two visits:
* The first visit by a psychiatrist for:
* information on the objectives and the methods of research, verification criteria for inclusion and non-inclusion and participation of obtaining consent (written consent)
* comprehensive psychiatric evaluation and procurement different scales (anxiety scale, Hamilton depression scale, evaluation of verbal IQ, ...).
* 2nd visit, a maximum of 15 days after the first visit by a psychologist, neuropsychologist for the award of the memories of love and future projections defining self: the experimenter asks the subjects to relate memories 3 and 3 future projections. It is important personal events that arouse strong emotions and that the subjects often think.
Memories and projections reported by the subjects are then classified according to their emotional valence, their content, significance and degree of integration itself.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PARALLEL
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Bipolar Disorder patients
psychological tests
Healthy Controls
psychological tests
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
psychological tests
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Men or women, right-handed, with a diagnosis of type 1 bipolar disorder, according to the DSM-IV criteria, aged from 18 to 60 years-old
* Native French speaker
* Affiliated to the social security
* Accepting the study after reading the information note and signing the consentment form
Healthy Controls (HC):
* Men or women, right-handed, aged from 18 to 65 years-old
* Native French speaker
* Affiliated to the social security
* Accepting the study after reading the information note and signing the consentment form
Exclusion Criteria
* A recent alcohol and/or drug abuse or dependence
* A significant general medical illness, including neurological disorders or head trauma
* A sensorial impairment (visual and/or hearing)
HC:
* A personal or first-degree-relative history of bipolar disorder, schizophrenia or schizoaffective disorder according to DSM-IV
* A recent alcohol and/or drug abuse or dependence
* A significant general medical illness, including neurological disorders or head trauma
* A sensorial impairment (visual and/or hearing)
18 Years
60 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
CHU de Reims
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chu Reims
Reims, France, France
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Delphine RAUCHER-CHENE
Role: primary
Sarah BARRIERE
Role: backup
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PA12064
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.