Behavioral and Cognitive Therapies for Auditory Hallucination Management

NCT ID: NCT03348787

Last Updated: 2020-07-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

55 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-12-13

Study Completion Date

2020-06-30

Brief Summary

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The present study wants to evaluate the efficacy of a short psychoeducational type group intervention and Cognitive behavioral therapy (CBT) 3rd wave on the severity of hallucinatory Acoustico-Verbal (HAV) symptomatology in patients with schizophrenia.

Detailed Description

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Conditions

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Chronic Psychosis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Behavioral and Cognitive Therapies

Chronic psychotic patients will have Behavioral and Cognitive Therapies

Group Type EXPERIMENTAL

Behavioral and Cognitive Therapies

Intervention Type BEHAVIORAL

Group intervention of 6 weekly sessions of one hour and 30 minutes based on the psychoeducational therapeutic principles and CBT type 3 wave "Accept Voices" applied to HAV

Interventions

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Behavioral and Cognitive Therapies

Group intervention of 6 weekly sessions of one hour and 30 minutes based on the psychoeducational therapeutic principles and CBT type 3 wave "Accept Voices" applied to HAV

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Schizophrenic disorders, schizo-affective disorders
* Suffering from persistent HAV
* No change in symptomatology for 3 months.
* No anticipated change in antipsychotic treatment (anti-hallucinatory): olanzapine, risperidone, amisulpride, quetiapine, aripiprazole, loxapine, haloperidol, clopixol, modecate, nozinan, cyamemazine, piportil, clozapine
* Major patient, or major incompetent.

Exclusion Criteria

* Mental retardation
* Subject participating in another search including an exclusion period still in progress at pre-inclusion
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Toulouse

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Axel Bourcier, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Toulouse

Locations

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Lannemezan Hospital

Lannemezan, , France

Site Status

Lavaur Hospital

Lavaur, , France

Site Status

Sainte-Marie de Rodez Hospital

Rodez, , France

Site Status

Ariège-Couserans Hospital

Saint-Lizier, , France

Site Status

Gérard Marchand Hospital

Toulouse, , France

Site Status

Countries

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France

Other Identifiers

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2017-A01929-44

Identifier Type: REGISTRY

Identifier Source: secondary_id

RC31/17/0159

Identifier Type: -

Identifier Source: org_study_id

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