Comparison of Antipsychotics for Metabolic Problems in Schizophrenia or Schizoaffective Disorder
This study is completed. It focuses on schizophrenia and currently lists study information in the United States.
SchizophreniaDrugFrom 18 Years to 65 Years
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
Then choose your country and confirm availability with each study site.
In plain English
Key information made simple
What is this study testing?
This study is testing whether Risperidone may be useful for adults experiencing schizophrenia.
What would participation involve?
Participants may receive Risperidone, attend study visits with the research team. The registry lists locations in the United States.
Who is it mainly for?
This study appears to be mainly for adults with schizophrenia.
What should you check before joining?
Ask about the dose, safety monitoring, and possible side effects, whether there is a comparison group, how many visits or travel steps are needed, the exact eligibility criteria.
Your next step
Check the study details
Check the official source, then confirm these points with the research team.
The overall study status can differ from each site's status. Open a country to see its locations and their registry status.
United States · 28 sites
SHANTI Clinical Trials
Colton, California
Site status: Not listed — confirm with the team
Stanford University
Palo Alto, California
Site status: Not listed — confirm with the team
Yale University
New Haven, Connecticut
Site status: Not listed — confirm with the team
Mental Health Advocates
Boca Raton, Florida
Site status: Not listed — confirm with the team
University of Miami School of Medicine
Miami, Florida
Site status: Not listed — confirm with the team
Emory University
Atlanta, Georgia
Site status: Not listed — confirm with the team
Medical College of Georgia
Augusta, Georgia
Site status: Not listed — confirm with the team
University of Iowa
Iowa City, Iowa
Site status: Not listed — confirm with the team
Clinical Research Institute
Wichita, Kansas
Site status: Not listed — confirm with the team
Lousiana State University Health Sciences Center
Shreveport, Louisiana
Site status: Not listed — confirm with the team
Clinical Insights
Glen Burnie, Maryland
Site status: Not listed — confirm with the team
Freedom Trail Clinic
Boston, Massachusetts
Site status: Not listed — confirm with the team
John C Corrigan Community Mental Health Center
Fall River, Massachusetts
Site status: Not listed — confirm with the team
University of Massachusetts
Worcester, Massachusetts
Site status: Not listed — confirm with the team
Wayne State University
Detroit, Michigan
Site status: Not listed — confirm with the team
University of Minnesota
Minneapolis, Minnesota
Site status: Not listed — confirm with the team
Washington University School of Medicine
St Louis, Missouri
Site status: Not listed — confirm with the team
New Mexico VA Healthcare System
Albuquerque, New Mexico
Site status: Not listed — confirm with the team
Research Foundation for Mental Hygiene
New York, New York
Site status: Not listed — confirm with the team
University of Rochester
Rochester, New York
Site status: Not listed — confirm with the team
John Umstead Hospital/Duke University
Butner, North Carolina
Site status: Not listed — confirm with the team
The University of North Carolina
Chapel Hill, North Carolina
Site status: Not listed — confirm with the team
Carolinas HealthCare System
Charlotte, North Carolina
Site status: Not listed — confirm with the team
University of Cincinnati
Cincinnati, Ohio
Site status: Not listed — confirm with the team
Philadelphia VA Medical Center-116A
Philadelphia, Pennsylvania
Site status: Not listed — confirm with the team
University of Texas Southwestern Medical Center
Dallas, Texas
Site status: Not listed — confirm with the team
Baylor College of Medicine
Houston, Texas
Site status: Not listed — confirm with the team
University of Texas Health Science Center at San Antonio
San Antonio, Texas
Site status: Not listed — confirm with the team
In practice
For you
Participation may contribute to research. Personal benefit is not guaranteed.
Ask the research team to explain the activities, time commitment, and follow-up involved.
Study sites are listed. Confirm the relevant site and any travel before making plans.
Important
Not medical advice
Information from public sources.
Are you the study sponsor? Contact us to update this page: hi@hopestage.com
FAQ
Questions about this study
What is this study trying to understand?
This study is exploring medication or study treatment for people with schizophrenia. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed. The detailed objective is not always clearly listed in the public registry; the study team can confirm.
Does this study involve a medication?
This appears to be a medication / drug study involving Risperidone, Olanzapine, Quetiapine, Aripiprazole. Phase 4 studies usually happen after treatment approval, to monitor real-world use.
Who might this study be for?
This study may concern people with schizophrenia; age range: From 18 Years to 65 Years. The criteria appear fairly broad, but you should not assume you are eligible. The study team must confirm diagnosis, age, exclusions, available locations, and next steps.
What would I likely need to do?
You may need to take a study treatment and have regular medical follow-up. The listed study locations suggest that at least part of participation may involve a physical site. Ask whether some steps can be done remotely.
What side effects, interactions, or treatment changes should I check?
If the study involves a medication, ask whether it is already approved, experimental, or being tested for a new use. Check possible side effects, interactions with current treatment, dose changes, monitoring, and what happens if you feel worse. For any mental health study, also ask who to contact if you feel worse, whether participation may affect current treatment, whether you can stop, and who confirms eligibility.
Will I need to travel or attend in-person visits?
The listed study locations suggest that at least part of participation may involve a physical site. Ask which sites are open, how many visits are expected, whether any steps can be done remotely, and whether travel costs or compensation are listed.
Who is behind this study?
This study is sponsored by National Institute of Mental Health (NIMH), which appears to be a government agency. Sponsor website: https://www.nimh.nih.gov. If available, it can be useful to check the sponsor website, collaborators, investigator affiliation, and the official registry before deciding. HopeStage does not judge the quality of a sponsor or researcher, but helps you identify what to verify.
Can I still join this study?
The public registry lists this study as not currently recruiting. This page remains available for information. Check the official record for the latest status and explore other recruiting studies.
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This EU register entry describes an interventional medicine trial, designed to assign participants a study treatment. The protocol sets out the treatment, eligibility criteria and assessments. Check the source details below for country statuses and any transfer to CTIS.
