Actively Recruiting

Phase 1
Age: 18Years +
All Genders
ID07239869

An AI Robot-assisted Tailored Activity Programme for Improving the Physical Inactivity of People With Dementia and Their Informal Caregivers

Led by The Hong Kong Polytechnic University · Updated on 2025-12-18

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating a robot-assisted tailored activity programme designed to improve physical inactivity in people with dementia and their informal caregivers. This pilot randomized controlled trial aims to test the feasibility and early effects of this programme on physical activity levels, self-confidence in physical activity, quality of life, neuropsychiatric symptoms, and psychological well-being. The study is conducted by The Hong Kong Polytechnic University and focuses on mild to moderate dementia cases and their caregiving partners. Participants are randomly assigned to one of two groups. The intervention group will receive a 12-week robot-assisted tailored activity programme, while the control group will continue with usual care provided by community centers. The tailored programme is designed specifically to address the needs of both the person with dementia and their caregiver, encouraging physical engagement and activity over the course of the study. Throughout the study, researchers will assess participants at the start and immediately after the 12-week period. They will measure changes in physical activity, self-efficacy related to physical activity, quality of life for both members of the caregiving dyad, neuropsychiatric symptoms in the person with dementia, and overall psychological well-being. The trial will also monitor the feasibility of implementing this robot-assisted programme. Participant involvement includes regular assessments and adherence to their assigned care pathway during the study period.

CONDITIONS

Brief Title

A Robot-assisted Tailored Activity Programme for People With Dementia and Their Caregivers

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • People with dementia who have mild to moderate dementia with a mini-mental state examination score higher than 10
  • People with dementia who can walk independently
  • People with dementia who are physically inactive as categorized by the International Physical Activity Questionnaire
  • People with dementia free from other medical or functional conditions limiting physical activity
  • Primary informal caregivers who live with the person with dementia
  • Caregivers who have provided care for more than six months
  • Caregivers who do not plan to send the care recipient to nursing homes in the next six months
  • Caregivers who are physically inactive
  • Caregivers who use a smartphone
Not Eligible

You will not qualify if you...

  • People with dementia who have a high risk of falling (Berg Balance Scale less than 45)
  • People with dementia not suitable for physical activity as recommended by their primary care physician
  • People with dementia currently involved in another interventional study involving physical exercise
  • People with dementia who had acute hospitalization more than three times in the past year
  • Caregivers with unstable physical or mental conditions
  • Caregivers who cannot communicate logically
  • Caregivers not suitable for physical activity as recommended by a primary care physician

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants in the intervention group receive a 12-week robot-assisted tailored activity programme, while those in the control group receive usual care provided by community centers.

Baseline and immediate post-intervention assessments

Trial Site Locations

Total: 1 location

1

The Hong Kong Polytechnic University

Hong Kong, Hong Kong

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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