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Self-Reports of Executive Functions in Persons With Parkinson's Disease and Their Significant Others

Self-Reports of Executive Functions in Persons With Parkinson's Disease and Their Significant Others

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04928027
Enrollment
100
Registered
2021-06-16
Start date
2021-06-08
Completion date
2022-06-08
Last updated
2021-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinsonism or Parkinson's Disease Nos

Brief summary

The investigators are conducting a study to compare the self-reports of executive functions (that is to say, what role cognitive processes such as working memory and attention) in persons with Parkinson's Disease to the reports of executive functions completed by their significant others. To conduct this study, the investigators need the participation of persons who are diagnosed with Parkinson's Disease and their significant others.

Detailed description

The purpose of this study is to explore the relationship between the self-reported executive functions (EFs) in persons with Parkinsons disease (PD) and their significant others. Executive functions include basic cognitive processes such as attention, inhibition, working memory, and cognitive flexibility. As this proposed study will test not only cognitive functioning, but specific aspects of it (i.e., EFs) without excluding persons with PD who have identified cognitive impairments, outcomes gathered could provide valuable information to better assist all types of persons with PD. Comparing their self-reported EFs to the EF ratings completedy by their signifiant others can help determine if a disparity exists between self-perceptions and actual observed EF abilties. This study would assess EFs through inhibition responses of participants via computerized versions the Comprehensive Executive Function Inventory-Adult Self-Report and Observer forms.

Interventions

None listed

Sponsors

Old Dominion University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
30 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

* For persons with PD,confirmed diagnosis of PD) For significant others - relationship with person with PD

Exclusion criteria

All participants will be screened to ensure they do not have: * any known cognitive disorders other than those associated with PD * impairments in vision that would affect their ability to safely participate in the study * recent history of neuromuscular injury/ damage that could affect their ability to complete the CEFI * the participant will be excluded if he or she is unable to follow commands well enough to complete the CEFI

Design outcomes

Primary

MeasureTime frameDescription
Comparison of EF outcomes1 yearResults of the self-reports of persons with PD and their Significant Others will be compared.

Countries

United States

Contacts

Primary ContactJane Roitsch, PhD
jroitsch@odu.edu2163347628

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026