Clinical trial

Genetic Studies of Early-onset Dementia

Name
AAAQ9793
Description
The aim of this study is to identify genetic factors that contribute to risk and progression of early-onset dementia (loss of memory function before the age of 70 years) across all ethnic groups, including Alzheimer's Disease, mild cognitive impairment and other dementias.
Trial arms
Trial start
2016-09-14
Estimated PCD
2028-04-30
Trial end
2028-04-30
Status
Recruiting
Treatment
Blood draw
Blood draw for identification of genetic variants associated with the development of memory problems
Arms:
Cognitively Healthy, Dementia/Alzheimer's Disease, Mild Cognitive Impairment
Neurocognitive testing
Brief memory test
Arms:
Cognitively Healthy, Dementia/Alzheimer's Disease, Mild Cognitive Impairment
Medical questionnaire
Collection of medical history
Arms:
Cognitively Healthy, Dementia/Alzheimer's Disease, Mild Cognitive Impairment
Size
1000
Primary endpoint
Genetic risk variants associated with early-onset dementia
2 years
Changes in blood biomarkers in early-onset dementia
2 years
Eligibility criteria
Inclusion criteria: * 18 years and older * Individuals diagnosed with dementia, their family members and unrelated healthy controls without dementia. Exclusion Criteria: -Individuals with competing diagnosis such as Huntington's disease, traumatic brain injury, drug or alcohol abuse, or schizophrenia, etc., unless family members of a dementia affected individual
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'PROSPECTIVE'}, 'bioSpec': {'retention': 'SAMPLES_WITH_DNA', 'description': 'Approximately 40ml of blood and/or saliva'}, 'enrollmentInfo': {'count': 1000, 'type': 'ESTIMATED'}}
Updated at
2024-04-09

1 organization