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CompletedNCT04292223

Effects of Treatment With Pimavanserin on Activities of Daily Living for Parkinson Disease Psychosis

This study is completed in the United States. It is testing effects of Treatment With Pimavanserin on Activities of Daily Living for Parkinson Disease Psychosis.

SchizophreniaDrugOver 40 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 the Effects of Treatment With Pimavanserin on Activities of Daily Living may be useful for adults experiencing schizophrenia.

What would participation involve?

Participants may receive the Effects of Treatment With Pimavanserin on Activities of Daily Living, 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.

View official study record (opens in a new tab)
  • Recruitment and eligibility

    Is a site open, and who can take part?

  • Visits and time

    Where are visits, can any be remote, and how much time is needed?

  • Costs and support

    What costs, reimbursement or compensation apply?

Before joining

Questions to ask before joining

Study clarity

Things to check before joining

Study start dateStarted: February 10, 2020
Recruitment status
Completed
Enrollment listed in the registry
29
Sponsor
ACADIA Pharmaceuticals Inc.
Sponsor type
Other organization
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
United States
Age range
Over 40 Years
Official registry ID
NCT04292223
Official title
A 16-Week Open-Label Study of the Effects of Treatment With Pimavanserin on Activities of Daily Living in Subjects With Parkinson's Disease Psychosis

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Study ID: NCT04292223. We help you review the study, but cannot decide medical eligibility.

Check recruitment and locations

Recruitment checked against the registry by HopeStage on . Registry information can change. Always confirm availability with the research team.

View official study record (opens in a new tab)

The overall study status can differ from each site's status. Open a country to see its locations and their registry status.

United States · 18 sites
  • Movement Disorders Center of Arizona
    Scottsdale, Arizona
    Site status: Not listed — confirm with the team
  • Neurology Center of North Orange County
    Fullerton, California
    Site status: Not listed — confirm with the team
  • Premier Clinical Research Institute, Inc.
    Miami, Florida
    Site status: Not listed — confirm with the team
  • Global Health Research Center, Inc.
    Miami Lakes, Florida
    Site status: Not listed — confirm with the team
  • Quantum Laboratories, Inc.
    Pompano Beach, Florida
    Site status: Not listed — confirm with the team
  • Parkinson's Disease Treatment Center of Southwest Florida
    Port Charlotte, Florida
    Site status: Not listed — confirm with the team
  • Accel Research Sites - Brain and Spine Institute
    Port Orange, Florida
    Site status: Not listed — confirm with the team
  • Infinity Clinical Research, LLC
    Sunrise, Florida
    Site status: Not listed — confirm with the team
  • Premiere Research Institute at Palm Beach Neurology
    West Palm Beach, Florida
    Site status: Not listed — confirm with the team
  • AU Movement and Memory Disorders
    Augusta, Georgia
    Site status: Not listed — confirm with the team
  • Maine Medical Partners Neurology
    Scarborough, Maine
    Site status: Not listed — confirm with the team
  • Wentworth Health Partners Coastal Neurology Services
    Dover, New Hampshire
    Site status: Not listed — confirm with the team
  • Bio Behavioral Health
    Toms River, New Jersey
    Site status: Not listed — confirm with the team
  • Neurology Diagnostics, Inc.
    Dayton, Ohio
    Site status: Not listed — confirm with the team
  • The Orthopedic Foundation
    New Albany, Ohio
    Site status: Not listed — confirm with the team
  • Central States Research
    Tulsa, Oklahoma
    Site status: Not listed — confirm with the team
  • KCA Neurology
    Franklin, Tennessee
    Site status: Not listed — confirm with the team
  • Neurological Associates of North Texas
    Dallas, 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 Pimavanserin. 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: Over 40 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 ACADIA Pharmaceuticals Inc., which appears to be another type of organization. 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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