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The objective of this study is to demonstrate the cognitive enhancement effect and safety of Tremella Fuciformis, using the cognitive and clinical indicators (e.g. memory, attention, and psychomotor speed) and the latest brain imaging methods for healthy adults suffering subjective cognitive impairment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| TF 600mg | Experimental | TF 600mg/day |
|
| TF 1200mg | Experimental | TF 1200mg/day |
|
| placebo | Placebo Comparator | placebo |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| TF 600mg | Dietary Supplement |
| ||
| TF 1200mg |
| Measure | Description | Time Frame |
|---|---|---|
| Changes from baseline in neurocognitive function (neurocognitive test batteries such as CANTAB) | Scores from neurocognitive test batteries such as CANTAB | baseline, 8th week |
| Changes from baseline in brain structure analyzed using the computational approach | Morphometric analysis of brain structures in magnetic resonance imaging | baseline, 8th week |
| Changes from baseline in brain function analyzed using the computational approach (Blood oxygenation level dependent (BOLD) signal intensity) | Blood oxygenation level dependent (BOLD) signal intensity and their connectivity assessed using functional magnetic resonance imaging scans | baseline, 8 week |
| Changes from baseline in brain biochemical metabolism analyzed using the computational approach (Brain metabolite concentrations assessed using magnetic resonance spectroscopy) | Brain metabolite concentrations assessed using magnetic resonance spectroscopy | baseline, 8th week |
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in Subjective Memory Complaints Questionnaire scores at 8th weeks | baseline, 8th week | |
| Number of participants with adverse events | 4th week | |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Ewha Womans University | Seoul | 120-750 | South Korea |
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| placebo | Dietary Supplement |
|
| Number of participants with adverse events |
| 8th week |