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NCT06483438Completed

Handwriting as an Objective Tool to Support the Identification of People With Alzheimer's Disease

Handwriting as an Objective Tool to Support the Identification of People With Alzheimer's Disease: Suitability of an Assessment Protocol

Source: ClinicalTrials.gov · Last updated 9 Aug 2024

Brief summary (registry, in English)

Alzheimer's disease (AD) is the most common of dementia, and has associated cognitive and motor disorders, with consequences on daily activities, including handwriting. Handwriting has been used to study fine motor control or executive functioning in healthy and unhealthy populations. Changes in this skill are present at different stages of the clinical course of Alzheimer's Disease. The sensorimotor deterioration is observed in handwriting tasks (motion kinematics, such as movement time, speed, and profiles) and brain activity rhythms. Handwriting has been used to study fine motor control or executive functioning in healthy and unhealthy populations, and changes in this skill are present at different stages of the clinical course of dementia. From a theoretical perspective, because sensorimotor deterioration observed in handwriting tasks (motion kinematics, such as movement time, speed, and profiles). Due to the large number of brain areas related to handwriting performance, brain electrical activity analysis can be an early indicator of brain dysfunction. Although there is a lack of validation across healthy and non-healthy populations Electroencephalogram (EEG) measures have the potential for evaluating cognitive performance. This research aims to analyze the suitability of the handwriting assessment protocol, which can contribute to a more in-depth knowledge of this subject and potentially support early identification and treatment.

Status (registry)
Completed
Study type
Observational
Enrollment
20 (actual)
First submitted
7 Jun 2024
Start date
2 Dec 2023
Primary completion date
30 Jul 2024
Lead sponsor
University of Évora
NCT number
NCT06483438

What you commit to

  • Study type: Observational
  • Participants enrolled: 20
  • From 2 Dec 2023 to the primary completion date, 30 Jul 2024
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • \- Previous neurological history (e.g. stroke, traumatic brain injury, multiple sclerosis, among others), psychiatric history or other incapacitating illnesses that could interfere with the collection of writing data. (NOTE that neurological disease is accepted in the dementia group, but co-morbidity of previous and actual neurological diseases will be excluded) Cognitively normal group

Other illness

  • \- Presence of neurological history (e.g., stroke, traumatic brain injury, multiple sclerosis, among others), psychiatric history, or other incapacitating illnesses that could interfere with the collection of writing data.

Who the study is looking for

  • Over 50 years of age
  • The inclusion criteria for the dementia group are as follows: patients diagnosed with dementia according to the DSM-5 criteria and cognitive impairment proven in the neuropsychological assessment
  • Portuguese native language
  • Over 50 years of age
  • At least three years of schooling

Criteria the registry did not label

  • Dementia group

Age in the registry: 50 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Espírito Santo Hospital of Évora
Coordinator of this site? Confirm its status
EvoraPortugalUnknown status
Casa dos Avós Residence
Coordinator of this site? Confirm its status
Ponte de SôrPortugalUnknown status
Costa Azul Residence
Coordinator of this site? Confirm its status
SesimbraPortugalUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.