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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| SMARTO ONE | Experimental |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SMARTO ONE | Drug | The SMARTO ONE® small molecule natural flavonoid compound product is provided by Beijing Jiafurui Biological Technology Co., Ltd. The intervention agent formula consists of extracts from Polygonum cuspidatum leaves, Fructus ligustri lucidi, Prunus mume, Semen ziziphi spinosae, celery, resistant maltodextrin, and steviol glycoside. Each package of the test product (3g) contains a total flavonoid content of 150mg. |
| Measure | Description | Time Frame |
|---|---|---|
| Montreal Cognitive Assessment (MoCA) | This outcome measure assesses cognitive ability and memory, with evaluation based on a scoring system.The total score ranges from 0 to 30 points, with scores lower than 26 indicating the presence of cognitive impairment. The lower the score, the more severe the disease. | 4 weeks |
| Pittsburgh Sleep Quality Index (PSQI) | The evaluation criteria for this outcome measure are as follows: 0-5 points indicate very good sleep quality; 6-10 points indicate average sleep quality; 11-15 points indicate poor sleep quality; 16-21 points indicate very poor sleep quality. | 4 weeks |
| Hamilton Anxiety Rating Scale (HAMA) | The evaluation criteria for this outcome measure are as follows: 0-6 points indicate no anxiety symptoms; 7-14 points indicate possible anxiety; 15-21 points indicate definite anxiety; 22-29 points indicate significant anxiety; and scores exceeding 29 points suggest severe anxiety. | 4 weeks |
| Hamilton Depression Scale(HAMD) | The evaluation criteria for this outcome measure are as follows:a score of less than 8 is normal, a score of 8-20 may indicate depression, a score of 21-35 may indicate depression, and a score of more than 35 may not indicate severe depression | 4 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Numerry of participating with adverse events | This is a safety outcome. | baseline, 4 weeks |
| Adverse event occurrence rate | This is a safety outcome. |
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Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Li Liu | Contact | 16619733315 | lily0496@126.com |
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| ID | Term |
|---|---|
| D019636 | Neurodegenerative Diseases |
| ID | Term |
|---|---|
| D009422 | Nervous System Diseases |
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|
| baseline, 4 weeks |
| Abnormality rate of routine blood tests | This is a safety outcome. Included in the outcome indicators are red blood cell count (WBC), haemoglobin concentration (Hb), white blood cell count (WBC), neutrophil count (Neut), lymphocyte count (Lymph), monocyte count (Mono), eosinophil count (Eos), basophil count (Baso) and platelet count (PLT). The abnormal blood count rate was obtained by dividing the number of people with abnormal blood counts by the total number of people with abnormal blood counts. | baseline, 4 weeks |
| Liver function-Alanine aminotransferase#ALT# | This is a safety outcome. | baseline, 4 weeks |
| Liver function-Aspartate aminotransferase (AST) | This is a safety outcome. | baseline, 4 weeks |
| Liver function-Total Protein(TP) | This is a safety outcome. | baseline, 4 weeks |
| Electrocardiogram | This is a safety outcome.This outcome measure primarily observes ST segment changes to evaluate the presence or improvement of myocardial ischemia. | baseline, 4 weeks |
| Body temperature | This is a safety outcome. | baseline, 4 weeks |
| Heart rate | This is a safety outcome. | baseline, 4 weeks |
| Number of breaths in 1 min | This is a safety outcome. | baseline, 4 weeks |
| Blood pressure-Diastolic blood pressure(mmHg) | This is a safety outcome. | baseline, 4 weeks |
| Blood pressure-Systolic blood pressure(mmHg) | This is a safety outcome. | baseline, 4 weeks |