Mild Cognitive Impairment
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants must meet all of the following four criteria to be included in this study: (1) Age 50–85 years; (2) No significant speech vision or hearing impairments and capable of completing neuropsychological assessments and related evaluations; (3) Sufficient comprehension ability to make independent judgments and fully understand the purpose content and procedures of the study; (4) Voluntary participation in the study willingness to cooperate in completing olfactory identification tests and cognitive function assessments and signing of an informed consent form.
Exclusion criteria
Exclusion criteria: Participants meeting any of the following criteria will be excluded: (1) Diagnosed with dementia or currently taking cognitive-enhancing medications; (2) Cognitive impairment caused by other conditions such as acute cerebrovascular disease central nervous system infections intracranial space-occupying lesions Parkinsons disease traumatic brain injury thyroid and parathyroid disorders diabetes poisoning epilepsy syphilis psychiatric disorders or severe vitamin deficiencies; (3) History of nasal fractures or nasal surgery or presence of olfactory dysfunction-related conditions (e.g. chronic rhinitis allergic rhinitis nasal polyps) or upper respiratory tract infection within the past two weeks; (4) Long-term or heavy exposure to volatile substances such as pesticides herbicides metal dust acid fumes industrial solvents cleaning products or sawdust; (5) History of drug abuse or heavy alcoholism within the past two years or long-term use of medications that affect cognitive function (e.g. corticosteroids antipsychotics sedative-hypnotics); (6) Pseudo-cognitive impairment due to mood disorders (e.g. moderate to severe depression) with a Hamilton Depression Scale (HAMD) score =18; (7) Intellectual disability or neurodevelopmental delay; (8) Current participation in other clinical trials involving cognitive interventions.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Montreal Cognitive Assessment(MoCA); | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical Dementia Rating(CDR);Activities of Daily Living(ADL;Mini-Mental State Examination(MMSE);Hamilton Depression Scale(HAMD);the Chinese Smell Identification Test(CSIT); | — |
Countries
China
Contacts
General Hospital of the Western Theater Command of the Chinese People's Liberation Army