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Clinical Trials/NCT03209778
NCT03209778
Terminated
Not Applicable

Involuntary Memories Investigation in Schizophrenia

University Hospital, Strasbourg, France1 site in 1 country65 target enrollmentSeptember 29, 2017
ConditionsSchizophrenia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenia
Sponsor
University Hospital, Strasbourg, France
Enrollment
65
Locations
1
Primary Endpoint
Autobiographical subjective score taking into account memories vividness and specifity
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

Patients with schizophrenia suffer from autobiographical memory disorders. Patients have difficulty to remember vividly personal past events when they are specifically asked for. Indeed, this task requires a good executive functioning to retrieve precise information stored in long term memory. Interestingly, executive functioning has been showed impaired in schizophrenia and studies showed that their autobiographical memory impairments were directed related to their executive dysfunction.

Yet, in daily life people remember more often autobiographical memories spontaneously, without trying voluntarily to recall them.

In that case, the involuntary recall of personal past events is much less sustained by executive functioning.

In this protocol the investigators would like to investigate and compare subjective characteristics of involuntary and voluntary autobiographical memories in order to highlight the role of executive dysfunction in patients' autobiographical memory impairments.

Registry
clinicaltrials.gov
Start Date
September 29, 2017
End Date
December 15, 2019
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Strasbourg, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • - for patients only
  • male or female
  • age limits : 18-55 years old
  • under the protection of health insurance
  • who have signed up the consent form
  • schizophrenia or schizo-affective disorder according to the DSM-5 criteria (APA, 2013).
  • clinically stable for at least 2 months
  • patients under guardianship or curatorship need agreement of their legal representative
  • informed of the results of prior medical examination for controls only
  • male or female

Exclusion Criteria

  • for both patients and controls
  • current severe or unstable somatic illness
  • neurological history (brain injury \> 15 minutes loss of consciousness , epilepsia, brain surgery...)
  • current substance use disorder (DSM-5)
  • current major depressive disorder (CDSS,BDI, HDRS)
  • mental retardation (IQ \< 70, WAIS-4, f-NART)
  • history of general anesthesia 3 months prior to the experiment
  • pregnancy declared by the subject
  • breast feeding
  • current legal control

Outcomes

Primary Outcomes

Autobiographical subjective score taking into account memories vividness and specifity

Time Frame: 8 months

Study Sites (1)

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