Actively Recruiting

Age: 15Years - 40Years
All Genders
ID04004364

Early-Phase Schizophrenia: Practice-based Research to Improve Outcomes

Led by Northwell Health · Updated on 2024-09-19

700

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

N

Northwell Health

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are working to create a learning health network focused on treating individuals experiencing their first episode of psychosis. This project builds on the success of the RAISE ETP study, which showed that a Coordinated Specialty Care (CSC) model could be effectively delivered in community mental health clinics across several states. The goal is to improve outcomes for people with early-phase schizophrenia by advancing CSC treatment and research. The treatment model being studied is Coordinated Specialty Care, a team-based approach that combines psychotherapy, support for employment and education, family education and support, and medication management. The project involves sites in five states—Connecticut, Florida, Michigan, Oklahoma, and South Carolina—that differ in the populations they serve and their research experience. These sites aim to implement practical assessments to enhance outcome tracking and conduct meaningful research. Participants are enrolled in CSC programs and contribute data over a five-year period. Researchers monitor the number of enrolled participants and collect information to improve care and outcomes related to first episode psychosis. The project focuses on practical, community-based treatment and assessment in real-world clinical settings, with ongoing engagement from multiple stakeholders.

CONDITIONS

Brief Title

Early-Phase Schizophrenia: Practice-based Research to Improve Outcomes

Who Can Participate

Age: 15Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Being enrolled in a Coordinated Specialty Care (CSC) program
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 5 years

Participants who are enrolled in a Coordinated Specialty Care (CSC) program are observed to assess outcomes related to first-episode psychosis treatment.

Trial Site Locations

Total: 1 location

1

Henderson Behavioral Health

Lauderdale Lakes, Florida, United States, 33319

Actively Recruiting

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Research Team

P

Patricia Marcy, BSN

C

Cristina Gonzalez, MS

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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