Effectiveness of Meta-Cognitive Training (EMC) in People With Psychosis of Brief Evolution.

NCT02340559 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 122

Last updated 2015-01-21

No results posted yet for this study

Summary

The purpose of this study is to assess the effectiveness of Meta-Cognitive Training (EMC) in people with a brief psychotic disorder, especially positive symptoms.

The secondary objectives would be to assess the effect of EMC on metacognition (cognitive distortions and deficits in theory of mind), psychosocial functioning and quality of life, neuropsychological functioning and gender, as well as determine the changes produced by EMC in the insight of each session and the maintenance of the effects of EMC program at six months of treatment.

Conditions

Interventions

BEHAVIORAL

Meta-cognitive Training

BEHAVIORAL

Psychoeducational group

Sponsors & Collaborators

  • Parc Sanitari Sant Joan de Déu

    collaborator OTHER
  • Corporacion Parc Tauli

    collaborator OTHER
  • Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

    collaborator OTHER
  • Fundación para la Investigación del Hospital Clínico de Valencia

    collaborator OTHER
  • Centre d'Higiene Mental Les Corts

    collaborator OTHER
  • Institut d´Assistència Sanitària Girona

    collaborator UNKNOWN
  • Servicio Andaluz de Salud de Granada, Málaga y Jaén

    collaborator UNKNOWN
  • Fundació Sant Joan de Déu

    lead OTHER

Principal Investigators

  • Susana Ochoa, PhD · Parc Sanitari Sant Joan de Déu

  • Marisa Barrigón, PhD · Servicio Andaluz de Salud. Granada

  • Fermín González · Servicio Andaluz de Salud. Jaen

  • Isabel Ruiz · Servicio Andaluz de Salud. Málaga

  • Eva Grasa · Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

  • Esther Pousa, PhD · Corporacion Parc Tauli

  • Esther Lorente, PhD · Hospital Clínic de València

  • Ana Barajas · Centre d'Higiene Mental de les Corts

  • Jordi Cid · Institut d'Assistència Sanitària de Girona

  • Raquel López, MS · Parc Sanitari Sant Joan de Déu

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2013-09-30
Completion
2014-12-31

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02340559 on ClinicalTrials.gov