Skip to main content
Clinical Trials/NCT01821469
NCT01821469
Completed
Not Applicable

Functional Correlates of Bipolar Disorders and Effects of the Psychoeducation. Assessment by Functional and Anatomic Neuroimaging.

University Hospital, Grenoble1 site in 1 country45 target enrollmentMay 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Conditions Influencing Health Status
Sponsor
University Hospital, Grenoble
Enrollment
45
Locations
1
Primary Endpoint
fMRI measurement (neurophysiological [fMRI - activation and functional connectivity])
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

This research project follows two main objectives: 1) Assess anatomical and functional cerebral abnormalities in bipolar disorder. 2) Evaluate anatomical and functional changes after the application of a psychoeducational program in these patients. Specifically, this project aims to assess neurophysiological (fMRI - activation and functional connectivity) and neuroanatomical (morphometry and diffusion tensor imaging) specificities related to bipolar disorders and the therapeutic response to the psychoeducation. The results of this thesis project would also contribute to the validation of a pathophysiological model of the bipolar disorder.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
December 2013
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University Hospital, Grenoble
Responsible Party
Principal Investigator
Principal Investigator

AdministrateurDRC

Professor

University Hospital, Grenoble

Eligibility Criteria

Inclusion Criteria

  • clinical diagnosis of bipolar disorders
  • euthymic (Montgomery and Asberg depression rating scale \< 10, Young Mania rating scale \< 10)

Exclusion Criteria

  • other concomitant psychiatric disorders

Outcomes

Primary Outcomes

fMRI measurement (neurophysiological [fMRI - activation and functional connectivity])

Time Frame: measurements were performed at T1 and T2 (up to 3 months)

measurements were performed before (T1) and after (T2) educational program of 12 sessions .One session last one hour and half once a week (they come at the hospital for all sessions : i.e. during 12 weeks). Thus, T1 to T2 is 3 months (average).

Study Sites (1)

Loading locations...

Similar Trials