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Parkinson DiseaseNCT06385184

Social & QoL Behaviors in Parkinson's Disease

An observational study of Parkinson Disease, run by Gregory Wallace at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Adults with Parkinson's Disease experience an array of challenges and changes in daily living, behaviors, and functioning throughout the progression of their condition. The investigators want to learn more about the effects of Parkinson's Disease on individuals' social behavior and quality of life (QoL) compared to… Read more about this study

Who is it for?
Ages 40 years and olderHealthy volunteers can take part
Conditions the study is for
Parkinson Disease
How many people
500 participants
Where
1 siteUnited States
Study dates
8 Mar 2024to 31 Dec 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: The study includes both 40+ year old adults with Parkinson's disease and 40+ year old neurotypical adults

Who may be able to join

  • Have been diagnosed with Parkinsons Disease by a healthcare professional
  • Are at least 40 years old
  • Are at least 40 years old

Who cannot join

  • Possess a diagnosis of autism or any other developmental disability (e.g., Down syndrome)
  • Neurotypical group
  • Have been diagnosed with Parkinson's disease by a healthcare professional
  • Possess a diagnosis of autism or any other developmental disability (e.g., Down syndrome)

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Gregory Wallace, PhD contact

202-994-8285

ladn@gwu.edu

United States1 site, 1 recruiting
  • The George Washington University

    Washington D.C., District of Columbia, 20052

    Gregory Wallace, PhD, 202-994-8285, ladn@gwu.edu

    Recruiting

Other trials in United States

About this study

Official title: Social Behaviors and Quality of Life in Individuals With Parkinson's Disease

Adults with Parkinson's Disease experience an array of challenges and changes in daily living, behaviors, and functioning throughout the progression of their condition. The investigators want to learn more about the effects of Parkinson's Disease on individuals' social behavior and quality of life (QoL) compared to people of the same age without Parkinson's Disease.

Being tested
No Intervention
Medical subject headings
Parkinson Disease

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • No InterventionOther

    Observational study with no intervention

Study groups in NCT06385184
Study groupRoleWhat they receive
Parkinson's diseaseThis group includes adults who: * Have been diagnosed with Parkinsons Disease by a healthcare professional * Are at least 40 years old and * Do not possess a diagnosis of autism or any other developmental disability (e.g., Down syndrome)
Receives: Other: No Intervention
Neurotypical adultsThis group includes adults who: * Are at least 40 years old * Do not have a diagnosis of Parkinsons Disease or any form of dementia and * Do not have a diagnosis of autism or any other developmental disability (e.g., Down syndrome)
Receives: Other: No Intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Subjective Quality of Life

    satisfaction with different aspects of life, such as health and social relationships

    Measured: through study completion, an average of 1 year

  2. Social Behavior

    ability to interact with others

    Measured: through study completion, an average of 1 year

  3. Activities of Daily Living

    ability to complete tasks to be independent

    Measured: through study completion, an average of 1 year

  4. Mental Health

    depression and anxiety symptoms

    Measured: through study completion, an average of 1 year

  5. Cognition

    memory and executive function challenges and strengths

    Measured: through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Apr 2024
  2. Study start8 Mar 2024
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06385184
Sponsor's protocol ID
NCR234859
Status last verified
Feb 2026
First submitted
18 Apr 2024
Last updated
13 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Currently, there is no plan to share participant data with other researchers.

Questions about this trial

What is this clinical trial studying?

An observational study of Parkinson Disease, run by Gregory Wallace at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 13 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Gregory Wallace, PhD (202-994-8285, ladn@gwu.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Subjective Quality of Life (time frame: through study completion, an average of 1 year). The study lists 5 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Feb 2026; AzTrials last refreshed its copy on 8 Nov 2026.

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