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Digital Measures of Neuropsychological Tests in AD patients

Completed
Conditions
Alzheimer's disease
dementia
10012272
Registration Number
NL-OMON47745
Lead Sponsor
Philips Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
160
Inclusion Criteria

For AD patient:
1. Aged 18 and older
2. Fluent/correct speaker in Dutch
3. AD patient is able to give consent
4. AD diagnosis by a clinical specialist, such as a geriatrician or neurologist
5. Being able to perform the neuropsychological tests with an Ipad
6. AD patient living at home (not at a nursing home)
7. Date of AD diagnosis < 2yr;For healthy participant:
1. Partner of relative of a patient with AD
2. Fluent/correct speaker in Dutch
3. Able to provide informed consent
4. Aged 18 and older

Exclusion Criteria

For AD patient;
1. Unable or incompetent to give written informed consent
2. Severe communication deficits
3. Unable and/or unwilling to use a tablet to perform the tests
4. Medical history of neurological and/or psychiatric disorders (except for AD)
5. Mild Cognitive Impairment (MCI), vascular dementia, frontotemporal or mixed dementia diagnosis
6. Traditional neuropsychological assessment in the last 6 months
7. Bad eyesight or hearing, even with correction
8. Unable to properly use hands
9. An average alcohol consumption of 4 or more units per day
10. Use of one or more of the following types of medicine: antipsychotics, benzodiazepines, antidepressants, opioids, lithium, anti-epileptics, anti- Parkinson medication
11. Use of drugs;For healthy participant:
1. Unable or incompetent to give written informed consent
2. Medical history of neurological and/or psychiatric disorders
3. Traditional neuropsychological assessment in the last 6 months
4. Bad eyesight or hearing, even with correction
5. Unable to properly use hands
6. An average alcohol consumption of 4 or more units per day
7. Use of one or more of the following types of medicine: antipsychotics, benzodiazepines, antidepressants, opioids, lithium, anti-epileptics, anti- Parkinson medication
8. Use of drugs

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Algorithmic outcome of the automated scoring of the tests mentioned and manual<br /><br>scoring of the tests </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>A list of measures that are significantly different for the two groups and a<br /><br>profile of combined measures that is significantly different for the two groups.<br /><br>Results of the questionnaire and interview of how the system was experienced by<br /><br>the two different groups and a list of recommendations on how the system can be<br /><br>improved for assessing people with Alzheimer*s Disease</p><br>
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