Brain Activity, Cerebral Blood Flow, Low-level Light Therapy, Mild Cognitive Impairment
Conditions
Brief summary
The primary objective of this study is to confirm and compare the effect of methods of Low-level light therapy (LED-T) in the mild cognitive impairment.
Detailed description
Total 168 patients were recruited and randomized to receive either real or sham-LED-T. Real experimental groups were divided into three groups; CA group, VA group, CA+VA dual group. Each group received LED-T (30 min) once a day for 30 days. Each groups LED-T positioned at following locations; * CA group on the superior border of the thyroid cartilage, and anterior to the sternocleidomastoid muscle based on Korea traditional therapy called Inyoung(ST9) * VA group on the upper abdomen, spinous process of the 2nd cervical vertebra upper margin based on Korea traditional therapy called CunChu * CA+VA dual group on the CA position (ST9), and VA position (BL10) The patients were initially evaluated at baseline, immediately, 4wks after intervention. Study type : Interventional Study Phase : Not provided Study Design : Allocation : Randomized Intervention Model : Parallel Assignment Masking : Single Blind (Investigator) Primary Purpose : Treatment, intervention Condition : Mild cognitive impairment, Health subjects Intervention : * Low-level light therapy device (Peak wavelength:610nm, Power intensity: 1.7mW/cm2, Energy density: 2.0J/cm2, Skin-adhesive light-emitting probes: spot size, 1cm diameter), * Parameters : Neuroimaging assessement: fMRI, SPECT, Neuropsychological behavioral assessment: SNSB; Seoul Neuropsychological screening battery, K-MoCA, Corsi-block test, K-MBI, K-ADL, GDS, EQ-5D, Neurophysiological assessment: MEP, Motor evoked potential, Gene test(BNDF, ApoE) Study Arms * Experimental : Sham control group and real stimulation group. * In each group, total sessions of the Low-level light therapy (LED-T) was done for intervention was followed after that. * Subjects received LED-T (30 min) once a day for 30 days. * The sham control group was kept without LED-T
Interventions
DEVICELow-level light therapy device
Peak wavelength:610nm, Power intensity: 1.7mW/cm2, Energy density: 2.0J/cm2, Skin-adhesive light-emitting probes: spot size, 1cm diameter
Sponsors
Samsung Medical Center
Yong-il Shin, MD
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
55 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
1. Subjects ages older than 55 years old 2. Subjects who has K-MoCA assessment score less than 23 3. Subjects who understand the purpose of the study and acquired the consent of the subjects or caregiver
Exclusion criteria
1. Subjects who have K-MMSE less than 19 2. Subjects who have pre-existing and present-existing neurological diseases as CNS lesion 3. Subjects who have psychiatric disease such as depression, schizophrenia, bipolar disease, or dementia 4. Subjects who is estimated as not appropriate for the study by the investigators
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Neuropsychological Behavioral Assessment 1 | Baseline, Change from Baseline SNSB at immediately after intervention , Change from Baseline SNSB at 4 weeks after intervention | SNSB |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Neuropsychological Behavioral Assessment 3 | Baseline, Change from Baseline K-MoCA at immediately after intervention , Change from Baseline K-MoCA at 4 weeks after intervention | K-MoCA |
| ADL assessment 1 | Baseline, Change from Baseline K-MBI at immediately after intervention , Change from Baseline K-MBI at 4 weeks after intervention | K-MBI |
| ADL assessment 2 | Baseline, Change from Baseline K-ADL at immediately after intervention , Change from Baseline K-ADL at 4 weeks after intervention | K-ADL |
| Depression assessment | Baseline, Change from Baseline GDS-SF at immediately after intervention , Change from Baseline GDS-SF at 4 weeks after intervention | GDS-SF |
| Neuropsychological Behavioral Assessment 2 | Baseline, Change from Baseline Corsi-block test at immediately after intervention , Change from Baseline Corsi-block test at 4 weeks after intervention | Corsi-block test |
| Gene test 1 | Baseline, Change from Baseline BNDF at immediately after intervention , Change from Baseline BNDF at 4 weeks after intervention | BNDF |
| Gene test 2 | Baseline, Change from Baseline ApoE at immediately after intervention , Change from Baseline ApoE at 4 weeks after intervention | ApoE |
| Neuroimaging Assessment 1 | Baseline, Change from Baseline fMRI at immediately after intervention , Change from Baseline fMRI at 4 weeks after intervention | fMRI |
| Neuroimaging Assessment 2 | Baseline, Change from Baseline SPECT at immediately after intervention , Change from Baseline SPECT at 4 weeks after intervention | SPECT |
| Quality of Life assessment | Baseline, Change from Baseline EQ-5D at immediately after intervention , Change from Baseline EQ-5D at 4 weeks after intervention | EQ-5D |
Countries
South Korea
Contacts
Primary ContactYong-il Shin, M.D, Ph.D
Outcome results
None listed