Multidomain Intervention Via a None-face-to-face Platform in Mild Cognitive Impairment

A multicenter clinical study to evaluate the efficacy and feasibility of a 24-week multidomain intervention via a none-face-to-face platform in mild cognitive impairment

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007184

Enrollment

100

Registered

2022-04-13

Start date

2022-03-22

Completion date

Unknown

Last updated

2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Behavioral : For 24 weeks, participants will receive cognitive training, physical exercise, nutrition education and education about vascular risk factor management using the tablet personal computer

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Subjects who completed end-of-study evaluation and participated in the preceding randomized controlled trial (RCT) "Multidomain Interventions Via Face-to-face and Video Communication Platforms in Mild Cognitive Impairment". 2. Being able to use the tablet PC through education, or having a person who can help a participant use the tablet PC. 3. Having a reliable informant who could provide investigators with the requested information 4. Provide written informed consent

Exclusion criteria

Exclusion criteria: 1. Major psychiatric illness such as major depressive disorders 2. Dementia 3. Other neurodegenerative disease (e.g., Parkinson's disease) 4. Malignancy within 5 years 5. Cardiac stent or revascularization within 1 year 6. Serious or unstable symptomatic cardiovascular disease 7. Other serious or unstable medical disease such as acute or severe asthma, active gastric ulcer, severe liver disease, or severe renal disease 8. Severe loss of vision, hearing, or communicative disability 9. Any conditions preventing cooperation as judged by the study physician 10. Significant laboratory abnormality that may result in cognitive impairment 11. Illiteracy 12. Unable to participate in exercise program safely 13. Coincident participation in any other intervention trial

Design outcomes

Primary

Measure	Time frame
total scale index score of Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)	—

Secondary

Measure	Time frame
Mini-Mental State Examination;Clinical Dementia Rating scale-Sum of Boxes;Prospective and Retrospective Memory Questionnaire;Geriatric Depression Scale-15 items;Quality of life-Alzheimer's disease;Bayer Activities of Daily Living;Nutrition Quotient for elderly;Short Physical Performance Battery;Self Determination Index;Pittsburgh Sleep Quality Index	—

Countries

Korea, Republic of

Contacts

Public ContactSeong Hye Choi

Inha University Hospital

seong7773@naver.com+82-32-890-3659

Outcome results