- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06385184
Social & QoL Behaviors in Parkinson's Disease
February 11, 2026 updated by: Gregory Wallace
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.
Study Overview
Study Type
Observational
Enrollment (Estimated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Gregory Wallace, PhD
- Phone Number: 202-994-8285
- Email: ladn@gwu.edu
Study Locations
-
-
District of Columbia
-
Washington D.C., District of Columbia, United States, 20052
- Recruiting
- The George Washington University
-
Contact:
- Gregory Wallace, PhD
- Phone Number: 202-994-8285
- Email: ladn@gwu.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The study includes both 40+ year old adults with Parkinson's disease and 40+ year old neurotypical adults
Description
Parkinson's disease group
Inclusion Criteria:
- Have been diagnosed with Parkinsons Disease by a healthcare professional
- Are at least 40 years old
Exclusion Criteria:
- Possess a diagnosis of autism or any other developmental disability (e.g., Down syndrome)
Neurotypical group
Inclusion Criteria:
- Are at least 40 years old
Exclusion Criteria:
- 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)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Parkinson's disease
This group includes adults who:
|
Observational study with no intervention
|
|
Neurotypical adults
This group includes adults who:
|
Observational study with no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subjective Quality of Life
Time Frame: through study completion, an average of 1 year
|
satisfaction with different aspects of life, such as health and social relationships
|
through study completion, an average of 1 year
|
|
Social Behavior
Time Frame: through study completion, an average of 1 year
|
ability to interact with others
|
through study completion, an average of 1 year
|
|
Activities of Daily Living
Time Frame: through study completion, an average of 1 year
|
ability to complete tasks to be independent
|
through study completion, an average of 1 year
|
|
Mental Health
Time Frame: through study completion, an average of 1 year
|
depression and anxiety symptoms
|
through study completion, an average of 1 year
|
|
Cognition
Time Frame: through study completion, an average of 1 year
|
memory and executive function challenges and strengths
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Gregory Wallace, PhD, George Washington University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 8, 2024
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2027
Study Registration Dates
First Submitted
April 18, 2024
First Submitted That Met QC Criteria
April 23, 2024
First Posted (Actual)
April 25, 2024
Study Record Updates
Last Update Posted (Actual)
February 13, 2026
Last Update Submitted That Met QC Criteria
February 11, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NCR234859
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Currently, there is no plan to share participant data with other researchers.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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