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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04354974
Other study ID # 10477M-ECO-DBP-2019
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date October 18, 2019
Est. completion date February 18, 2023

Study information

Verified date July 2020
Source Centre hospitalier de Ville-Evrard, France
Contact Youcef BENCHERIF
Phone 0782723674
Email youcef.bencherif@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Psychotherapeutic management of cognitive disorders in patients suffering from a mood disorder


Recruitment information / eligibility

Status Recruiting
Enrollment 36
Est. completion date February 18, 2023
Est. primary completion date February 18, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

1. Age between 18 and 65 years old

2. The patient's previous diagnosis of Bipolar-Related Disorder or Depressive Disorder according to the DSM-5 criteria.

3. Mood stabilized with respect to depressive symptomatology (absence or presence of residual mild depressive symptoms (HDRS-17 = 18))

4. Mood stabilized with respect to manic symptomatology (absence or presence of residual mild manic symptoms (YMRS = 8))

5. Stable and effective treatment at minimum dose for at least 2 months

6. Cognitive complaint expressed by the patient, and detected by the patient's referring psychiatrist

7. Free and Informed Consent Form read, initialled and signed

8. Patient affiliated to a social protection scheme or beneficiary of State Medical Aid

9. Patient knowing how to speak French -

Exclusion Criteria:

1. Presence of a DSM-5 disorder, other than a mood, anxiety or personality disorder

2. Substance addiction or abuse (Alcohol, psychoactive substances) in the past 12 months

3. Manic, hypomanic or major depressive episode in the last 2 months

4. Somatic or neurological disorder which may lead to cognitive impairment

5. Current or less than one month's commitment to another research protocol

6. A neuropsychological assessment prior to 6 months.

7. Patient under protective custody, guardianship or reinforced guardianship

Study Design


Related Conditions & MeSH terms

  • Mood Disorders
  • Taking Charge of Cognitive Impairment in Patients With Mood Disorders

Intervention

Behavioral:
Evaluation
Evaluation of a cognitive remediation program for mood disorders

Locations

Country Name City State
France Youcef Bencherif Neuilly sur Marne

Sponsors (1)

Lead Sponsor Collaborator
Centre hospitalier de Ville-Evrard, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary the Perceptual Reasoning Index (PRI) the Wechsler Intelligence Scale. Increase in the Perceptual Reasoning Index (PRI) of the Wechsler Adult Intelligence Scale - Fourth Edition [WAIS-IV] significantly different between the two study groups. at 1 year