Cognitive impairment memory complaints
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Clinical diagnose of Mild Cognitive Impairment (MCI) or Alzheimer's Disease (patient group) Normal age-related cognitive functioning (control group) Age 55 yrs and over
Exclusion criteria
Exclusion criteria: Bodyweight of >180 kg. History of severe cardiovascular and neurological disorders, traumatic brain injury, mental retardation or muscle disorders. Use of cholinesterase inhibitors or Memantine. Contraindicators of HUTT. Subjects who cannot stand up actively by themselves or are immobile.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study parameter is autonomic function (cardiovascular measures of autonomic function derived from continuous BP and ECG signals) during HUTT in MCI/AD vs control. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary parameters will be effects of changes in BP on CBF; differences in complexity measures in cardiovascular and cerebrovascular signals (BP, ECG, CBFV and NIRS) in rest and during HUTT between MCI/AD and controls. | — |
Countries
Netherlands