The Management of Schizophrenia in Clinical Practice (MOSAIC)

November 1, 2016 updated by: Genentech, Inc.

A Prospective, Non-Interventional Registry of Diverse Patients With Schizophrenia Across the Disease Spectrum in Usual Care Settings: Course of Disease, Treatments, and Burden of Illness

This study is a disease-based registry designed to follow patients with a DSM-IV-TR (Diagnostic and Statistic Manual of Mental Disorders, Text Revision) diagnosis of schizophrenia, schizoaffective disorder, or schizophreniform disorder treated in usual care settings for up to 5 years. The registry seeks to describe the course of disease in schizophrenia, including cognitive function and negative symptoms, its treatment, and its burden of disease for participants, caregivers, clinicians, and society as a whole.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
557

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • California
      • Granada Hills, California, United States, 91344
      • Los Angeles, California, United States, 90095-6968
      • Santa Monica, California, United States, 90403
    • Connecticut
      • Cedar Rapids, Connecticut, United States, 6514
      • New Haven, Connecticut, United States, 06519
    • Florida
      • Chicago, Florida, United States, 60653
      • Gainesville, Florida, United States, 32608
      • Gainesville, Florida, United States, 32601
      • Gainesville, Florida, United States, 32608-1197
      • Jacksonville, Florida, United States, 32209
      • Lake City, Florida, United States, 32025
      • Miami, Florida, United States, 33136
      • Miami, Florida, United States, 33125
    • Illinois
      • Chicago, Illinois, United States, 60611
    • Iowa
      • Iowa City, Iowa, United States, 52242
      • Iowa City, Iowa, United States, 52240
      • Iowa City, Iowa, United States, 52242-1000
    • Massachusetts
      • Belmont, Massachusetts, United States, 02478
    • Minnesota
      • Minneapolis, Minnesota, United States, 55454
      • St. Paul, Minnesota, United States, 55107
      • St. Paul, Minnesota, United States, 55114
    • New York
      • New York, New York, United States, 10032
      • New York, New York, United States, 11004
      • New York, New York, United States, 10029
      • New York, New York, United States, 10035
      • New York, New York, United States, 10018
      • New York, New York, United States, 10040
      • Orangeburg, New York, United States, 10962
    • North Carolina
      • Carrboro, North Carolina, United States, 27510
      • Cary, North Carolina, United States, 27513
      • Chapel Hill, North Carolina, United States, 27514
      • Durham, North Carolina, United States, 27707
      • Durham, North Carolina, United States, 27713
      • Durham, North Carolina, United States, 27704
      • Hillsborough, North Carolina, United States, 27278
      • Pinehurst, North Carolina, United States, 28374
    • Ohio
      • Cincinnati, Ohio, United States, 45219
    • Texas
      • Lytle, Texas, United States, 78052
      • Round Rock, Texas, United States, 78664
      • San Antonio, Texas, United States, 78202
      • San Antonio, Texas, United States, 78284-7792
      • Taylor, Texas, United States
    • Utah
      • Salt Lake City, Utah, United States, 84106
    • Washington
      • Tacoma, Washington, United States, 98493

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients with schizophrenia, schizoaffective disorder, or schizophreniform across the disease spectrum treated in usual care settings

Description

Inclusion Criteria:

  • Adult patients, >/= 18 years of age
  • DSM-IV-TR diagnosis of schizophrenia, schizoaffective disorder, or schizophreniform disorder
  • Participants presenting with the normal course of care in usual treatment settings
  • Able to read and speak English
  • Able and willing to provide informed consent
  • Able and willing to comply with the study protocol

Exclusion Criteria:

  • Participants enrolled as subjects in clinical trials at registry enrollment
  • Participants anticipating they will be unable to participate in regularly scheduled assessments as per protocol

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort

Group / Cohort

A group or subgroup of participants in an observational study that is assessed for biomedical or health outcomes.
Cohort

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Time Frame
Positive and Negative Symptoms of Schizophrenia (PANSS)
Time Frame: up to 5 years
up to 5 years
Clinical Global Impression Schizophrenia Scale (CGI-SCH)
Time Frame: up to 5 years
up to 5 years
Cognitive function (Fluency, Digit Symbol-Coding, Trail Making Test)
Time Frame: up to 5 years
up to 5 years

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Time Frame
Negative Symptom Assessment Scale (NSA4)
Time Frame: up to 5 years
up to 5 years
Pharmacologic/behavioural treatments used in usual care settings: intervention
Time Frame: up to 5 years
up to 5 years
Pharmacologic/behavioural treatments used in usual care settings: dose
Time Frame: up to 5 years
up to 5 years
Pharmacologic/behavioural treatments used in usual care settings: duration
Time Frame: up to 5 years
up to 5 years
Personal and Social Performance (PSP)
Time Frame: up to 5 years
up to 5 years
Schizophrenia Quality of Life Scale (SQLS)
Time Frame: up to 5 years
up to 5 years
Schizophrenia Caregiver Questionnaire
Time Frame: up to 5 years
up to 5 years
Maslach Burnout Inventory (MBI)
Time Frame: up to 5 years
up to 5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Genentech, Inc.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
December 1, 2012

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
May 1, 2014

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
May 1, 2014

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
December 4, 2012

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
December 6, 2012

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
December 10, 2012

Study Record Updates

Last Update Posted (Estimate)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
November 2, 2016

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
November 1, 2016

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
November 1, 2016

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • ML28264

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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