Black and African Americans Connections to Parkinson's Disease (BLAAC PD)

NCT ID: NCT06719583

Last Updated: 2024-12-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

2000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-11-16

Study Completion Date

2026-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

BLAAC PD is a research study to understand what Parkinson's disease looks like for Black and African American communities.

BLAAC PD is happening at research centers around the United States. The study is part of the Global Parkinson's Genetics Program (GP2). GP2 is a research project working to transform understanding of the genetics of Parkinson's disease and make that knowledge globally relevant.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Research studies have found connections between genes and Parkinson's disease (PD). But those results have mostly come from studies with non-Black or African American volunteers. BLAAC PD aims to learn more about gene changes that may cause Parkinson's in Black and African American people. Study volunteers at sites across the United States will attend one visit and will give either a blood or saliva sample, complete a smell test, and may be asked to complete a physical exam. This new data could lead to future Parkinson's tests and treatments for Black and African American people and it may help better understand disease in other groups, too.

This pioneering initiative will fill a gap of knowledge about PD in Black and African American people.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Parkinson Disease

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

genetics racial health disparities

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Participants with Parkinson's Disease

Data collected from these participants include demographic information and family health history. Participants may also complete a physical exam. Participants also complete a smell test and contribute a blood or saliva sample for genetic analyses.

No interventions assigned to this group

Control Participants

Data collected from these participants include demographic information and family health history. Participants also complete a smell test and contribute a blood or saliva sample for genetic analyses.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Ability to provide informed consent
* Age 18 years or older
* Self-identify as Black or African American


* Ability to provide informed consent
* Age 18 years or older
* Self-identify as Black or African American
* Meet the Movement Disorder Society's clinical diagnostic criteria for Parkinson's disease

Exclusion Criteria

* Diagnosis of Parkinson's Disease and/or neurological condition
* Familial history of PD and/or neurodegenerative or psychiatric conditions
* Unknown family history of PD and/or neurodegenerative or psychiatric conditions
* Any conditions that, in the investigator's opinion, preclude the individual's ability to carry out study activities
* If submitting a saliva sample, nothing by mouth (food, drink, gum, tobacco, or smoking) for 30 minutes prior to sample collection


\- If submitting a saliva sample, nothing by mouth (food, drink, gum, tobacco, or smoking) for 30 minutes prior to sample collection
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Institutes of Health (NIH)

NIH

Sponsor Role collaborator

University of Chicago

OTHER

Sponsor Role collaborator

University of Alabama at Birmingham

OTHER

Sponsor Role collaborator

Rush University

OTHER

Sponsor Role collaborator

Washington University School of Medicine

OTHER

Sponsor Role collaborator

Medical University of South Carolina

OTHER

Sponsor Role collaborator

University Hospitals Cleveland Medical Center

OTHER

Sponsor Role collaborator

Louisiana State University Health Sciences Center Shreveport

OTHER

Sponsor Role collaborator

University of Florida

OTHER

Sponsor Role collaborator

University of Maryland

OTHER

Sponsor Role collaborator

The University of Texas Health Science Center, Houston

OTHER

Sponsor Role collaborator

Ochsner Health System

OTHER

Sponsor Role collaborator

Michael J. Fox Foundation for Parkinson's Research

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Andrew Singleton, PhD

Role: PRINCIPAL_INVESTIGATOR

National Institutes of Health (NIH)

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Alabama at Birmingham

Birmingham, Alabama, United States

Site Status RECRUITING

University of Florida

Gainesville, Florida, United States

Site Status RECRUITING

Rush University

Chicago, Illinois, United States

Site Status RECRUITING

University of Chicago

Chicago, Illinois, United States

Site Status RECRUITING

Ochsner Clinic Foundation

New Orleans, Louisiana, United States

Site Status RECRUITING

Louisiana State University Health Sciences Center Shreveport

Shreveport, Louisiana, United States

Site Status RECRUITING

University of Maryland

Baltimore, Maryland, United States

Site Status RECRUITING

Kaiser Permanente Midatlantic States

Rockville, Maryland, United States

Site Status ACTIVE_NOT_RECRUITING

Washington University in St. Louis

St Louis, Missouri, United States

Site Status RECRUITING

University Hospitals Cleveland Medical Center

Cleveland, Ohio, United States

Site Status RECRUITING

Medical University of South Carolina

Charleston, South Carolina, United States

Site Status RECRUITING

University of Texas Health Science Center, Houston

Houston, Texas, United States

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United States

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Naomi Louie, MPH RDN

Role: CONTACT

Phone: 212-509-0995

Email: [email protected]

J Solle, MBA

Role: CONTACT

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Joseph Richardson

Role: primary

Lauren Ruffrage

Role: backup

Marissa Dean, MD

Role: backup

David Standaert, MD, PhD

Role: backup

Randy Foli

Role: primary

Kyle Rizer

Role: backup

Ashley Rawls, MD

Role: backup

Lauren Fanty, MD

Role: backup

Tracy Tholanikunnel, MD

Role: backup

Jacqueline Vanegas

Role: primary

Deborah Hall, MD

Role: backup

Crystal Mercado

Role: primary

Tao Xie, MD, PhD

Role: backup

Mahesh Padmananban, MD

Role: backup

Dominique Thomas

Role: primary

Julia Staisch, MD

Role: backup

Sarah Breaux, MD

Role: backup

Mackenzie Williams

Role: primary

Elizabeth Disbrow, PhD

Role: backup

Christina Griffin

Role: primary

Rebecca Weimer

Role: backup

Lisa Shulman, MD

Role: backup

Rainer von Coelln, MD

Role: backup

Coordinator

Role: primary

Scott Norris, MD

Role: backup

Erin Foster, PhD, OTD-L

Role: backup

Ashley Hawkins

Role: primary

Camilla Kilbane, MD

Role: backup

Mohamed Elkasaby, MD

Role: backup

Lisa Heidelberg

Role: primary

Vanessa Hinson, MD

Role: backup

Andrew Ameri, MD

Role: backup

Natalia Pessoa Rocha

Role: primary

Erin Furr Stimming, MD

Role: backup

Shivika Chandra, MD

Role: backup

Natalia Pessoa Rocha, PhD

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

BLAAC PD

Identifier Type: -

Identifier Source: org_study_id