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Clinical Trials/NCT02038465
NCT02038465
Unknown
Not Applicable

REMEDIATION COGNITIVE DE LA MÉMOIRE AUTOBIOGRAPHIQUE DANS LA SCHIZOPHRENIE AU MOYEN DE SENSECAM

University Hospital, Strasbourg, France1 site in 1 country80 target enrollmentMay 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia Cognition Autobiographical Memory Cognitive Remediation
Sponsor
University Hospital, Strasbourg, France
Enrollment
80
Locations
1
Primary Endpoint
Specificity of memories recovered by using the SenseCam camera during the trial
Last Updated
7 years ago

Overview

Brief Summary

The aim of the study is to assess the efficiency of SenseCam® in patients with schizophrenia by comparing two cognitive remediation methods of autobiographical memory.Patients and control participants will be invited to carry SenseCam® during 7 hours per day minimum and for 4 successive days. Each ending day when carry SenseCam®, they will be asked to go to the laboratory where 4 types of interventions will be successively done according to the randomization: 1) a simple visual retrospective procedure (SVR), 2) a visual retrospective procedure coupled with a specific cueing intervention (VR-SC), 3) a verbal retrospective (VbR) and 4) no intervention (control condition).The testing phase will take place 14 days after the last day of data collection and will consist in a cued recall task and a recognition task using the pictures obtained by the SenseCam® of the participants.According to our hypotheses, the vividness of memories will be higher in events subjected to the VR-SC procedure than in events subjected to the SVR and VbR procedures. This effect is expected for both patients with schizophrenia and controls participants. Since strategies to enrich memory details will be explicitly given to the patients when using the VR-SC procedure, we assume that patients will be able to normalize their scores.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
December 2019
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Strasbourg, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • for both patients and controls
  • male or female willing to participate and who have signed up the legal document
  • under the protection of health insurancefor patients only
  • schizophrenia or schizo-affective disorder according to the DSM-IV
  • TR criteria
  • clinically stable for at least 2 monthsfor controls only
  • no psychiatric history

Exclusion Criteria

  • for both patients and controls
  • current severe or unstable somatic illness
  • neurological history (epilepsia, brain injury, brain surgery...)
  • current substance use disorder (DSM-IV-TR)
  • current major depressive disorder (DSM-IV-TR)
  • mental retardation (IQ \< 70)
  • pregnancy, breast feeding
  • current legal controlfor patients only
  • treatment comprising benzodiazepines
  • benzodiazepines intake during the last 3 weeksfor controls only

Outcomes

Primary Outcomes

Specificity of memories recovered by using the SenseCam camera during the trial

Time Frame: 1 month

Test the effectiveness of two techniques of cognitive remediation of autobiographical memory using an innovative tool called SenseCam.This specificity will be evaluated by the experimenter by scoring wealth in detail memories reported during the cued recall task

Study Sites (1)

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