- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05791006
Neuropsychology of Financial Capacity (NEUROFIN)
The present project aims to investigate the financial capacity in patients diagnosed with Parkinson's Disease or parkinsonism, brain tumor (glioma or meningioma) and cerebrovascular lesion (stroke), in order to evaluate the presence and degree of impairment, and the role of some factors as potential predictors of financial incapacity.
The term 'financial capacity' means both operations relating, for example, to asset management or investing money, and activities of daily life such as shopping or using small sums of money; these activities are mediated by different cognitive functions, from numerical and arithmetic skills to decision making. Financial capacity is, in fact, an instrumental activity of daily life (i.e. Instrumental Activity Of Daily Living, I-ADL) whose impairment negatively affects the functional autonomy of the individual, so as to be subject to legal protection.
To assess financial capacity, the Numerical Activities of Daily Living - Financial (NADL-F; Arcara et al., 2017) will be administered, a battery of tests aimed at investigating both financial performance and financial competence according to the most recent neuropsychological models proposed in the literature.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Nadia Bolognini, PhD
- Phone Number: 8132 +39025821
- Email: n.bolognini@auxologico.it
Study Locations
-
-
Lombardia
-
Milan, Lombardia, Italy, 20122
- Recruiting
- Istituto Auxologico Italiano IRCCS
-
Contact:
- Nadia Bolognini, PhD
- Phone Number: 8132 +39025821
- Email: n.bolognini@auxologico.it
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
- Patients with Parkinson's Disease/parkinsonisms
- Patients with brain tumor
- Patients with stroke
- Healthy controls
Description
Inclusion Criteria:
- age > 18 years
- Clinical diagnosis of interest for clinical groups
- For stroke patients: disease duration > 1 month
Exclusion Criteria:
- Other brain disorders different from those of interest
- Sensory-motor deficits that could prevent neuropsychological assessment
- Language disorders that could prevent neuropsychological assessment
- Global cognitive impairment as indexed by MoCA < 26 or MMP < 22.85
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy Controls
|
Neuropsychological assessment with:
|
|
Patients with brain tumors
|
Neuropsychological assessment with:
|
|
Patients with Parkinson's Disease/Parkinsonisms
|
Neuropsychological assessment with:
|
|
Patients with ischemic or haemorrhagic stroke
|
Neuropsychological assessment with:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numerical Activity of Daily Living Financial (NADL-F) in Patients with Parkinson's Disease/Parkinsonisms
Time Frame: At baseline
|
Assessment of financial capacity; score range=0-62; higher scores indicate higher financial capacities
|
At baseline
|
|
Numerical Activity of Daily Living Financial (NADL-F) in Patients with ischemic or haemorrhagic stroke
Time Frame: At baseline
|
Assessment of financial capacity; score range=0-62; higher scores indicate higher financial capacities
|
At baseline
|
|
Change from baseline in Numerical Activity of Daily Living - Financial (NADL-F)Patients with brain tumors
Time Frame: At 3 and 12 months follow up
|
Assessment of financial capacity; score range=0-62; higher scores indicate higher financial capacities
|
At 3 and 12 months follow up
|
|
Montreal Cognitive Assessment (MoCA)
Time Frame: At baseline
|
Assessment of global cognitive functioning
|
At baseline
|
|
Frontal Assessment Battery (FAB)
Time Frame: At baseline
|
Assessment of global cognitive functioning
|
At baseline
|
|
Activities of daily living questionnaire (ADL)
Time Frame: At baseline
|
Assessment of function independence in everyday life
|
At baseline
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 25C121
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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