A study for examination of effectiveness and feasibility of a personalized dementia prevention program based on individual risk factors

A study for examination of effectiveness and feasibility of a personalized dementia prevention program based on individual risk factors in non-demented middle- to old-aged adults

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0009437

Enrollment

Registered

2024-05-17

Start date

2024-02-23

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

None listed

Interventions

Behavioral : The dementia prevention program comprises a total of 24 weeks, divided into an intensive program (12 weeks) and a maintenance program (12 weeks). The intervention group participates in a

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Diagnosed as cognitively normal or with mild cognitive impairment at Seoul National University Hospital's Dementia Clinic within the past 3 months. Individuals who wish to participate in the program and meet all of the following criteria: 1. Age: 45 years or older 2. Education: At least 0 years of formal education (able to read and write) 3. Possession of two or more of the following dementia risk factors: A. Has not engaged in moderate-intensity exercise for more than 150 minutes per week within the past year (Moderate-intensity exercise: Exercise at an intensity greater than brisk walking for at least 150 minutes per week) B. Has not read books/newspapers/magazines at least once a week within the past year C. Has not met with close acquaintances such as friends/relatives/neighbors at least once a week within the past year D. Has felt consistently sad or lacked enthusiasm within the past year 4. Owns a mobile phone and is capable of sending and receiving text messages as well as watching videos.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with dementia. 2. Unable to participate in the program due to severe physical/mental conditions (progressive cancer, severe internal medical conditions, immobility, Severe vision and hearing impairment, etc.). 3. Currently participating in another non-pharmacological intervention program.

Design outcomes

Primary

Measure	Time frame
Modified Australian National University Alzheimer’s Disease Index: ANU-ADRI	—

Secondary

Measure	Time frame
CERAD Total Score;Risk Factor composite z-score;PSQI-K;Korean version of the Geriatric Depression Scale and its short form; SGDS-K;Depression Anxiety Stress Scale-21; DASS-21;K-CD-RISC ;Revised UCLA Loneliness Scale;Medical outcomes study-social support survey (MOS-SSS)	—

Countries

Korea, Republic of

Contacts

Public ContactHwajo Lee

Seoul National University Hospital

yghm2204@naver.com+82-2-2072-3155

Outcome results