An Integrated Program for the Treatment of First Episode of Psychosis

Completed · Not applicable

Conditions studied: Schizophrenia, Schizoaffective Disorder, Schizophreniform Disorder, Brief Psychotic Disorder, Psychotic Disorder NOS

In brief

The purpose of this study is to determine how services should be provided to reduce symptoms and improve life functioning for adolescents and adults who have been recently diagnosed with schizophrenia.

Key facts

Study ID

NCT01321177

Run by

Northwell Health

People needed

404

Starts

2010-07-01

Expected to finish

2017-07-01

Last updated by the study team

2021-10-26

Who can join

Age: 15 and older, up to 40. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Confirmed SCID DSM-IV clinical diagnosis by trained remote clinical assessor of:
• schizophrenia, schizoaffective disorder, schizophreniform disorder, brief psychotic disorder, psychotic disorder NOS
• Any duration of untreated psychosis
• Any ethnicity
• Ability to participate in research assessments in English
• Ability to provide fully informed consent (assent for those under age 18)

You may not qualify if…

• Inability to understand what research participation entails or correctly answer the questions about research participation that are part of the Study Information Review and provide fully informed consent
• More than 4 months of prior cumulative treatment with antipsychotic medications
• Diagnosis of bipolar disorder, psychotic depression or substance-induced psychotic disorder
• Current psychotic disorder due to a general medical condition
• Current neurological disorders that would affect diagnosis or prognosis. These would include, but are not limited to seizure disorders, dementing or degenerative disorders, lesions or substantial congenital abnormalities. In most cases, disorders such as headache disorders would not require protocol exclusion
• Clinically significant head trauma
• Any other serious medical condition that in the opinion of the investigator would seriously impair functioning making the patient unsuitable for the trial

Where it is running

• San Fernando Mental Health Center — San Fernando, California, United States
• Santa ClaritaMental Health Center — Santa Clarita, California, United States
• Mental Health Center of Denver — Denver, Colorado, United States
• United Services Inc. — Willimantic, Connecticut, United States
• Henderson Mental Health Center — Fort Lauderdale, Florida, United States
• Life management Center of Northwest Florida — Panama City, Florida, United States
• Central Fulton Community Mental Health Center — Atlanta, Georgia, United States
• Cobb County Community Services Board — Austell, Georgia, United States
• Park Center — Fort Wayne, Indiana, United States
• Community Mental Health Center, Inc. — Lawrenceburg, Indiana, United States
• Eyerly Ball — Des Moines, Iowa, United States
• Terrebonne Mental Health Center — Houma, Louisiana, United States
• River Parish Mental Health Center — Laplace, Louisiana, United States
• Catholic Social Services of Washtenaw County (CSSW) — Ann Arbor, Michigan, United States
• Touchstone Innovare — Grand Rapids, Michigan, United States
• Clinton-Eaton-Ingham Community Mental Health Authority — Lansing, Michigan, United States
• Human Development Center — Duluth, Minnesota, United States
• North Point Health and Wellness — Minneapolis, Minnesota, United States
• Pine Belt Mental Health Clinic — Hattiesburg, Mississippi, United States
• Burrell Behavioral Health — Columbia, Missouri, United States
• UMKC School of Pharmacy — Kansas City, Missouri, United States
• Burrell Behavioral Health — Springfield, Missouri, United States
• Community Alternatives — St Louis, Missouri, United States
• Community Mental Health Center of Lancaster County — Lincoln, Nebraska, United States
• The Mental Health Center of Greater Manchester — Manchester, New Hampshire, United States

Full record on ClinicalTrials.gov

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