Cost-utility Study of a Group of Compensatory Cognitive Remediation in Schizophrenia

NCT02879604 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 218

Last updated 2025-09-30

No results posted yet for this study

Summary

Significant cognitive impairment (executive functions, memory, attention) is common in schizophrenia affecting up to 80% of patients. But pharmacological treatments (typical and atypical antipsychotic) do not have impact on cognitive functioning. For over 20 years, alternative non-pharmacological therapeutics have been developed in schizophrenia. These techniques called cognitive remediation specifically target cognitive deficits. The first cognitive remediation available for patients was designed to stimulate new learning, or relearning, of cognitive tasks, and thus to improve certain deficient domains. These procedures were efficient in improving cognition as measured by neurocognitive tests but their impact on functioning and daily life was weak. In a second time, compensatory remediation has been developed. Compensatory approaches seek to make improvements in the patient's functioning by avoiding areas of impairment and recruiting other intact cognitive domains or by creating a supportive external environment. In recent meta-analysis compensatory remediation has larger effect-size than classical cognitive remediation, with an impact on patients psychosocial functioning. Recently, Dr E. Twamley (University of California) developed and tested a group-based, manualized, compensatory cognitive training intervention.

Compensatory cognitive training (CCT) is a low-tech, brief intervention and is easily transposable in community care. Our team translated this method into French. The investigators planned a cost -utility study between CCT and treatment as usual in schizophrenia patients with less than 10 years of evolution.

Conditions

Interventions

OTHER

Compensatory cognitive training

In addition to the usual care, method of compensatory cognitive remediation

OTHER

Usual

Usual care

Sponsors & Collaborators

  • Assistance Publique Hopitaux De Marseille

    collaborator OTHER
  • University Hospital, Clermont-Ferrand

    collaborator OTHER
  • Assistance Publique - Hôpitaux de Paris

    collaborator OTHER
  • Hôpital Louis Mourier

    collaborator OTHER
  • Centre Hospitalier Charles Perrens, Bordeaux

    collaborator OTHER_GOV
  • University Hospital, Strasbourg

    collaborator OTHER
  • Hospital Center Alpes-Isère

    collaborator OTHER
  • Hôpitaux à Bron

    collaborator OTHER
  • Fondation FondaMental

    collaborator OTHER
  • University Hospital, Montpellier

    lead OTHER

Principal Investigators

  • Delphine DC CAPDEVIELLE, MD-PhD · Montpellier University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2018-03-05
Primary Completion
2023-03-28
Completion
2023-03-28

Countries

  • France

Study Locations

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Entities

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 NCT02879604 on ClinicalTrials.gov