CBB Satisfaction Survey

Cheng Sheng Chen

Status: Completed

Conditions: Alzheimer Disease; Cognitive Impairment

Study type: Observational

Funder types: Other

Identifiers

NCT06496347

CBB-TWSS-21

Details and patient eligibility

About

The Cogstate Brief Battery (CBB) is a computerized measure for cognitive screening that consists of four cognitive tasks to assess psychomotor function, attention, learning, and working memory, and provides an easy-to-interpret report without the need for manual scoring. Clinical trials and research studies have proven the validity of CBB for cognitive assessment and distinguish MCI or dementia from normal aging.

Participants express a growing acceptance of the use of computerized tests for detecting cognitive impairment, viewing it as a potential tool to improve quality of patient care and the patient-clinician relationship when used in conjunction with the "human touch." The CBB utilizes non-verbal playing-card stimuli in order to minimize language, educational and cultural biases affecting performance. It has the advantages of being portable (adaptable to notebooks, tablets, and even smart phones), short (20-30 min), game-like in presentation and thus motivating, and cross-culturally adaptable. The CBB is well liked in waiting rooms of primary care settings. It is assumed that the CBB will also be highly accepted by Taiwanese.

Enrollment: 192 patients

Sex: All

Ages: 50 to 85 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

For MCI/dementia groups:

Inclusion criteria:

1. Patient diagnosed with MCI, AD dementia, VaD or DLB
2. Participant who is 50-85 years of age
3. Taiwanese who had finished primary education
4. Participant (or legally acceptable representative) who signed the written ICF

Exclusion criteria:

1. Participant with GDS score ≥ 10
2. Participant with CDR score > 1 (Assessment result within 6 months can be used conditionally.)
3. Participant with MMSE score ≤ 17 (MMSE score will be converted from CASI score. Assessment result within 6 months can be used conditionally.)
4. Participant diagnosed with Schizophrenia
5. Participant diagnosed with Parkinson's disease
6. Participant diagnosed with cancer (except basal cell skin carcinoma) in the past two years
7. Participant diagnosed with uncontrolled diabetes
8. Participant with regular alcohol use exceeding two standard drinks per day for women or four per day for men (one standard drink corresponds to 350 cc of beer)
9. Participant unable to take CBB test according to the investigator's discretion, such as blindness
10. Participant who, in the opinion of the investigator or medical monitor, should not participate in the study

For HC group:

Inclusion criteria:

1. Healthy volunteers without objective cognitive impairment
2. Participant who is 50-85 years of age
3. Taiwanese who had finished primary education
4. Participant who signed the written ICF

Exclusion criteria:

1. Participant with GDS score ≥ 10
2. Participant diagnosed with Schizophrenia
3. Participant diagnosed with Parkinson's disease
4. Participant diagnosed with cancer (except basal cell skin carcinoma) in the past two years
5. Participant diagnosed with uncontrolled diabetes
6. Participant with regular alcohol use exceeding two standard drinks per day for women or four per day for men (one standard drink corresponds to 350 cc of beer)
7. Participant unable to take CBB test according to the investigator's discretion, such as blindness
8. Participant who, in the opinion of the investigator or medical monitor, should not participate in the study

Trial design

192 participants in 2 patient groups

healthy control (HC) group,

Description:

no intervention(s)

MCI/dementia group

Description:

no intervention(s)