Skip to main content
Clinical Trials/NCT05164289
NCT05164289
Terminated
Not Applicable

Interest of EMDR (Eye Movement Desensitization and Reprocessing) Psychotherapy in the Management of Schizophrenic Disorders

Hôpital NOVO2 sites in 1 country6 target enrollmentDecember 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Schizophrenic Disorders
Sponsor
Hôpital NOVO
Enrollment
6
Locations
2
Primary Endpoint
Assessment of the decrease in the severity of positive or negative symptoms of schizophrenia
Status
Terminated
Last Updated
3 years ago

Overview

Brief Summary

The purpose of this study is to determine the interest of the use of EMDR (Eye Movement Desensitization and Reprocessing) psychotherapy in the management of psychotic disorders, in particular schizophrenic disorders.

Detailed Description

Since 2015 more and more studies conducted by researchers, especially Dutch and English, are interested in the use of EMDR (Eye Movement Desensitization and Reprocessing) for other pathologies such as bipolar disorder, unipolar depression, anxiety disorders, psychotic disorders, substance use disorders and chronic pain. These studies show that EMDR appears to be a technique that is both effective, capable of significantly improving symptoms, and without risk for patients, while respecting the protocol and the clinical stabilization provided during the procedure. To date, the use of EMDR for the management of psychotic patients has not been the subject of any prospective study in France and the authors' conclusions converge on the fact that it is essential to carry out more research on the subject. For this, the investigators wish to evaluate the effect of EMDR on the management of patients with schizophrenic disorders, on the basis that this psychotherapy would improve their quality of life (improvement of all the specific scores used in psychiatry). : PANSS, DES, HAD and WEMWBS scales). Finally, the investigators believe that it is relevant to assess the benefit of EMDR six months after hospitalization of patients, in order to measure the maintenance of this efficacy in the medium term

Registry
clinicaltrials.gov
Start Date
December 10, 2021
End Date
April 27, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Hôpital NOVO
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • ≥ 18 years and over,
  • Hospitalized for decompensated psychotic disorder, Positive diagnosis of schizophrenia or schizoaffective disorder (according to the DSM-V psychiatry manual),
  • With positive or negative symptoms according to the Positive and Negative Syndrome Scale (PANSS),
  • Stabilized clinical condition (considered compatible with hospital discharge),
  • With ambulatory follow-up planned after hospitalization

Exclusion Criteria

  • \< 18 years,
  • Patients who do not meet the diagnostic criteria (according to the DSM-V psychiatry manual) for schizophrenic or schizoaffective disorder),
  • Non-French speaking or illiterate patients,
  • Cognitive disorders making it impossible the understanding and the none- opposition to the study,
  • Non-stabilized clinical condition (incompatible with hospital discharge),

Outcomes

Primary Outcomes

Assessment of the decrease in the severity of positive or negative symptoms of schizophrenia

Time Frame: At 6 month after Hospital discharge (M0)

The decrease in the severity of positive or negative symptoms of schizophrenia is assessed using the "Positive and Negative Syndrome Scale" (PANSS) between M0 and M6.This decrease will be considered effective if it's greater than or equal to 20%.

Secondary Outcomes

  • Assessment of the decrease in the intensity of anxiety and depressive symptoms.(At 6 month after Hospital discharge (M0))
  • Assessment of the decrease in the intensity of dissociative symptoms.(At 6 month after Hospital discharge (M0))
  • Quality of life assessment(At 6 month after Hospital discharge (M0))

Study Sites (2)

Loading locations...

Similar Trials