KCT0007317
Completed
未知
Verification of symptom improvement effect in elderly people with cognitive decline through inhalation of phytocide.
Hallym University Medical Center- Chuncheon0 sites68 target enrollmentTBD
ConditionsMental and behavioural disorders
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Mental and behavioural disorders
- Sponsor
- Hallym University Medical Center- Chuncheon
- Enrollment
- 68
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Adults over 55 years of age.
- •2\) Those who meet the diagnostic criteria for mild cognitive impairment or early Alzheimer's dementia.
- •(CDR 0\.5\-2 or GDS 2\-5, and memory complaint, normal activities of daily living, normal general cognitive function, abnormal memory for age and, not demented patients with mild cognitive impairment or Alzheimer's disease)
- •3\) A patient who can read and understand the subject's explanation and consent form, and is capable of language skills at a level that can respond to questionnaires.
- •4\) A patient who has voluntarily decided to participate in this clinical trial and who has consented in writing to the informed consent form and can participate in the entire clinical trial period.
Exclusion Criteria
- •(1\) Persons diagnosed with bipolar or psychotic major depressive disorder.
- •(2\) Persons with a history of uniaxial psychiatric disorders including intellectual disability, schizophrenia, alcoholism, and bipolar disorder.
- •(3\) Stroke, convulsive disease, Parkinson's disease, multiple sclerosis, cerebral palsy, Huntington's disease, encephalitis, meningitis, liver disease beyond cirrhosis, kidney disease to the extent of requiring dialysis, etc. that may interfere with completion of this cognitive training program; patient with medical condition.
- •(4\) Those with a history of convulsions.
- •(5\) Those who have found other neurological abnormalities that may cause memory impairment during medical examination.
- •(6\) When it is judged that there is a problem in attaching EEG and DC stimulation electrodes due to scalp deformity, inflammatory reaction, or other dermatological problems.
- •(7\) Those who have had cancer in the past 3 years.
- •(8\) Those who have undergone cerebrovascular surgery, such as brain surgery or carotid artery surgery.
- •(9\) Persons who have abused drugs in the past 5 years.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Not yet recruiting
Not Applicable
Comparison of two proton pump inhibitor therapy approaches for laryngopharyngeal reflux disease treatmentDiseases of th respiratory systemKCT0004871Hallym University Medical Center-Dongtan72
Not yet recruiting
Not Applicable
Study on the improvement of clinical symptoms and mechanism of acupuncture in amyotrophic lateral sclerosisITMCTR2024000135Capital Medical University
Completed
Not Applicable
Validation of improvement of several symptoms and alteration of facial flora by application of creamHealthy adultJPRN-UMIN000031417SOUKEN Co.,Ltd15
Recruiting
Not Applicable
Comparative study of symptom improvement effect of vonoprazan and esomeprazole in patients with reflux esophagitis.Reflex esophagitisJPRN-UMIN000028962Ikoma Gastorenteroproctorogy Clinic40
Completed
Not Applicable
A confirmation study for the improvement effect of skin quality by the test food consumptioot applicableJPRN-UMIN000037734CPCC Company Limited110