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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04737096
Other study ID # 201601789A0C603
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date January 1, 2020
Est. completion date January 2, 2023

Study information

Verified date January 2023
Source Chang Gung Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a 24-week randomized, double-blind, placebo-controlled trial. We will enroll patients with aMCI or mild AD. All patients will receive 2 weeks of tDCS (5 sessions per week, 10 sessions in total) during the first 2 weeks of the study, and will also be allocated randomly to either of 2 treatment groups for 24 weeks: (1) DAOIB group; (2) placebo group. We will assess the patients every 8 weeks during the treatment period (weeks 0, 8, 16, and 24). We hypothesize that augmentation with DAOIB will yield better effect than tDCS alone in improving the cognitive function, global functioning and quality of life in patients with aMCI or mild AD.


Recruitment information / eligibility

Status Completed
Enrollment 97
Est. completion date January 2, 2023
Est. primary completion date January 2, 2023
Accepts healthy volunteers No
Gender All
Age group 50 Years to 100 Years
Eligibility Inclusion Criteria: - Clinical diagnosis of Alzheimer's disease or mild cognitive impairment - MMSE between 10-26 - CDR 1 or 0.5 Exclusion Criteria: - Hachinski Ischemic Score > 4 - Substance abuse/dependence - Parkinson disease, epilepsy, dementia with psychotic features - Major depressive disorder - Major physical illnesses - Severe visual or hearing impairment

Study Design


Related Conditions & MeSH terms

  • Dementia
  • Transcranial Direct Current Stimulation

Intervention

Drug:
DAOIB
The DAOIB dose will be adjusted every 8 weeks according to clinical evaluation.
Placebo
placebo
Device:
tDCS
tDCS

Locations

Country Name City State
Taiwan Kaohsiung Chang Gung Memorial Hospital Kaohsiung

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in the Alzheimer's disease assessment scale - cognitive subscale at week 8, 16 and 24 Alzheimer's disease assessment scale-cognitive subscale scores range from 0 (best) to 70 (worst) week 0, 8, 16, 24
Secondary Change from baseline in Clinician's Interview-Based Impression of Change plus Caregiver Input score at week 8, 16 and 24 Change from baseline in Clinician's Interview-Based Impression of Change plus Caregiver Input score at week 8, 16 and 24 week 8, 16, 24
Secondary Change from baseline in Mini-Mental Status examination score at week 8, 16 and 24 Change from baseline in Mini-Mental Status examination score at week 8, 16 and 24 week 0, 8, 16, 24
Secondary Change from baseline in Alzheimer's disease Cooperative Study scale for ADL in MCI (ADCS-MCI-ADL) score at week 8, 16 and 24 The assessment appears to be a suitable instrument for evaluating activities of daily living in early-phase dementia. Its scores range from 0 (worst) to 78 (best) week 0, 8, 16, 24
Secondary Change from baseline in Quality of life score at week 8, 16 and 24 Quality of life will be assessed by Medical Outcomes Study Short-Form-36 (SF-36). The SF-36 consists of eight sections: (1) vitality, (2) physical functioning, (3) bodily pain, (4) general health perceptions, (5) physical role functioning, (6) emotional role functioning, (7) social role functioning, and (8) mental health. week 0, 8, 16, 24
Secondary Change from baseline in the composite score of a battery of additional cognitive tests at week 24 The battery of additional cognitive tests include speed of processing (Category Fluency), working memory (Wechsler Memory Scale, Spatial Span), verbal/nonverbal learning and memory tests (Wechsler Memory Scale, Word Listing) week 0, 24
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