Validation of a Tool for the Dimensional Assessment of Apathy in a Population Suffering From Schizophrenia.

NCT ID: NCT03801551

Last Updated: 2020-10-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 105 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-03
• Study Completion Date: 2020-10-22

Brief Summary

Schizophrenia affects about 1% of the world's population. According to the WHO, it was one of the ten most worrying pathologies of the twenty-first century. The situation of psychic disability that results impacted the entire life course. This disease is characterized by positive symptoms (delirium, hallucination, psychotic agitation) and negative symptoms and disorganization (destructuring of thought, language and behavior). Cognitive disorders are easily measurable in the spectrum of schizophrenia and are quantifiable with some tools to measure the level of performance of the individual in different areas.

In these patients apathy is found in one out of two cases (prevalence of 51%), so it is a widespread negative symptom. Apathy corresponds to a pathology of voluntary action that can exist in different forms, resulting from the alteration of one or more mechanisms. It is a predictor of functional outcomes, regardless of positive symptoms or depression.

Studies of people with head injuries have found a link between frontal cognitive impairment and apathy. The recognition, the identification of the dimensional mechanisms of apathy and the understanding of the links with cognitive disorders are therefore a major issue in the improvement of the functional prognosis. Moreover, these mechanisms are currently little studied in the spectrum of schizophrenia.

There are currently questionnaires to show the presence or absence of apathy, such as the Apathy Evaluation Scale or the Lille Apathy Rating Scale. However most scales offer a global apathy score and the proposed treatments are limited due to the difficulty in identifying the dimensions and understanding of the underlying mechanisms of their own.

The potentiality of apathy to become a source of disability is now widely recognized. It is therefore important to consider the expression of this handicap in terms of the repercussions that this disorder may have on the daily lives of patients. There are questionnaires to measure the functional autonomy of patients with a psychic disorder. Apathy is also an obstacle to supporting patients in psychiatry.

The lack of knowledge and underestimation of apathy and its mechanisms in schizophrenia, in addition to overworking the psychiatric health sector, favor a drift towards the institutionalization of the person, with its medico-economic consequences on the system.

Conditions

Schizophrenia

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Patient

Group Type: EXPERIMENTAL

Validate according to psychometric criteria, a dimensional measure of apathy in a population suffering from schizophrenia spectrum disorder and other psychotic disorders (according to DSM-5 criteria).

Intervention Type: DIAGNOSTIC_TEST

Validate according to psychometric criteria, a dimensional measure of apathy in a population suffering from schizophrenia spectrum disorder and other psychotic disorders (according to DSM-5 criteria).

Interventions

Validate according to psychometric criteria, a dimensional measure of apathy in a population suffering from schizophrenia spectrum disorder and other psychotic disorders (according to DSM-5 criteria).

Validate according to psychometric criteria, a dimensional measure of apathy in a population suffering from schizophrenia spectrum disorder and other psychotic disorders (according to DSM-5 criteria).

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Men or women between 18 and 55 years old
• According to the DSM-5 criteria: spectrum of schizophrenia and other psychotic disorders (excluding psychotic disorder induced by a substance, drug or other medical condition as well as schizotypal personality disorder) in relation to the medical file and confirmed by the MINI test.
• Stable symptomatology (clinical assessment) during the month prior to inclusion
• Substantive psychotropic treatment unchanged during the month prior to inclusion (25% change).
• Reading and writing in French acquired.
• Persons who received informed information about the study and who co-signed, with the investigator, a consent to participate in the study
• After signing the consent by persons under guardianship, signed consent for participation by the tutor.
• For persons under guardianship, signature of the consent under the curator's assistance.
• Affiliate or Social Security Entitlement

Exclusion Criteria

• IQ score < 70 (intellectual disability measured by f-NA)
• Neurological disorders of vascular, infectious or neurodegenerative origin, dyschromatopsia.
• Taking somatic drugs with a cerebral or mental impact (eg corticosteroids).
• Resistance to neuroleptics.

Addiction to cannabis, alcohol or other substances (> 2 / week) according to DSM-5 criteria, except tobacco.

• Simultaneous participation in a remediation program targeting neurocognitive deficits.
• Refusal of consent of the person.
• For persons under guardianship: refusal of consent of the legal representative for participation in this study.
• For persons under curatorship: no information of the legal representative for participation in this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Centre Hospitalier de Niort

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

LISE M'BAREK

Role: STUDY_DIRECTOR

Centre Hospitalier de Niort - France

Locations

Centre Hospitalier Esquirol

Limoges, , France

Centre Hospitalier de Niort

Niort, , France

Countries

France

Other Identifiers

CH-NIORT-CREHPSY-01-2017

Identifier Type: -

Identifier Source: org_study_id