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Exploring the Impact of Dementia Prevention Programs Using Robots as Intervention Tools on Community Elderly

Exploring the Impact of Dementia Prevention Programs Using Robots as Intervention Tools on Community Elderly

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06984458
Enrollment
80
Registered
2025-05-22
Start date
2025-04-18
Completion date
2025-11-21
Last updated
2026-04-17

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

Conditions

Aging and Cognitive Health, Cognitive Decline, Dementia, Mild Cognitive Impairment (MCI), Psychological Well-being

Keywords

Robot-delivery intervention, Dementia prevention, Dementia, Community elderly

Brief summary

The purpose of this study is to intervene in the cognitive functions of the community elderly through the "Robot Dementia Prevention Course" training. It is expected that through the eight-week course design activities, the cognitive functions, social activities, emotional management (such as alleviating depression), well-being, reduce loneliness and can be achieved, thereby preventing or delaying cognitive decline. This study is a quasi-experimental design. It adopts pre-test and post-test methods for the experimental group and the control group. Before the intervention of the "Robotic Dementia Prevention Course", the community elderly were given a pre-test. After receiving an 8-week course (two months), the first post-test will be conducted, and three months later, the second post-test (post-post-test) will be conducted to analyze the delay effect. The experimental group conducted a two-month "Robot Dementia Prevention Course" intervention. The research subjects were 40 people. Each group of 5 people was assigned a Kebbi robot. The course intervention was divided into 8 groups. The Kebbi robot mainly taught and communicated with the elderly interactively. There is a well-trained teaching assistant in the class to enhance the learning effect of the elderly. The two classes per week are about 2 hours long, with 50 minutes of course knowledge introduction, 10 minutes of rest, 50 minutes of interaction with Kebbi Artificial Intelligence-based board games, and 10 minutes of prize-based quizzes after class. They are held once a week, with a total of 8 weeks of courses (duration two months), classes were taken in the elderly's original care center or long-term care base; the control group did not receive any course intervention. Statistical methods were analyzed using SPSS version 23.0, and descriptive statistics, paired t tests, generalized estimating equations, etc. were used to test the changes before and after the intervention.

Interventions

BEHAVIORALRobot Dementia Prevention Course

It is expected that through the eight-week course design activities, the cognitive functions, social activities, emotional management (such as alleviating depression), well-being, reduce loneliness and can be achieved, thereby preventing or delaying cognitive decline. The experimental group conducted a two-month "Robot Dementia Prevention Course" intervention. The research subjects were 40 people. Each group of 5 people was assigned a Kebbi robot. The course intervention was divided into 8 groups. The Kebbi robot mainly taught and communicated with the elderly interactively. There is a well-trained teaching assistant in the class to enhance the learning effect of the elderly. The two classes per week are about 2 hours long, with 50 minutes of course knowledge introduction, 10 minutes of rest, 50 minutes of interaction with Kebbi Artificial Intelligence-based board games, and 10 minutes of prize-based quizzes after class.

Sponsors

National Taiwan Normal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age 65 years or older, Able to communicate in Mandarin or Taiwanese, Able to provide informed consent or have a legal guardian provide consent

Exclusion criteria

* Diagnosis of severe dementia or advanced neurodegenerative disease, Severe psychiatric disorders (e.g., schizophrenia, bipolar disorder), Unconsciousness or inability to stay awake or focused for the session duration, Inability to comply with study protocol or scheduled sessions

Design outcomes

Primary

MeasureTime frame
Change in Cognitive Function Assessed by SPMSQParticipants will complete the SPMSQ at baseline, post-intervention (week 8), and follow-up (week 20).
Change in Depression Symptoms Assessed by GDS-15The instrument will be administered at baseline, post-intervention (week 8), and follow-up (week 20).
Change in Social Engagement and Activities Assessed by SEAQThe instrument will be administered at baseline, post-intervention (week 8), and follow-up (week 20).
Change in Psychological Well-being Assessed by WHO-5The instrument will be administered at baseline, post-intervention (week 8), and follow-up (week 20).
Change in loneliness Assessed by UCLA Loneliness ScaleThe instrument will be administered at baseline, post-intervention (week 8), and follow-up (week 20).

Countries

Taiwan

Contacts

STUDY_CHAIRJong-Long Guo, PhD

National Taiwan Normal University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 18, 2026