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OpenTrials
Completed

NCT Number: NCT01206842

Social Cognition Training in Schizophrenia

People with schizophrenia show deficits in social cognition, the ability to process information about other people such as identifying their emotional expressions. Social cognition is associated with everyday life functioning and could therefore be an important treatment target. Several social cognitive training programs have been developed during the last years. Results indicate that social cognitive performance can be ameliorated through commonly used intervention techniques. However, it is less clear whether this improvement generalizes to everyday life. The purpose of this study is to investigate if a social cognitive training program (Training in Affect Recognition) improves performance on social cognitive and neuropsychological tests and leads to improved everyday life functioning in persons with schizophrenia. The study also aims at examining if an improvement is present three months after completion of the training intervention.

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Key information

Age range

18 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Oslo University Hospital

Oslo, 0424, Norway

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age 18-55
  • diagnosis of schizophrenia or schizoaffective disorder
  • IQ > 69
  • sufficient mastery of Norwegian to undergo assessments

Exclusion criteria

  • history of head trauma
  • neurological/medical condition known to interfere with central nervous system
  • receiving outpatient care at time of recruitment

Treatment and study plan

Training in Affect Recognition

Other

A 12-session social cognitive training programming covering emotion perception and social perception administered in a group setting to up to four participants with schizophrenia at the time

Primary outcomes

  1. Social cognitive tests

    Time frame: Within one week and within three months of completed training

    PFA and MASC

Secondary outcomes

  1. Functional capacity tests

    Time frame: Within one week and within three months of completed training

    AIPSS and UPSA-brief

  2. Neuropsychological tests

    Time frame: Within one week and within three months of completed training

    MATRICS

Sponsors and collaborators

Lead sponsor

Oslo University Hospital

Other

Registry information

Important dates

Study start
2011
Primary completion
2018
Study completion
2018
First posted
Sep 22, 2010
Registry last updated
May 22, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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