Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06597981

Development and Testing of a Dyadic Empowerment-based Sport Stacking Program to Improve Health Outcomes of People With Mild Dementia and Their Family Caregivers

Led by The University of Hong Kong · Updated on 2025-11-20

144

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating an 18-week dyadic empowerment-based sport stacking program designed to improve health outcomes for people with mild dementia and their family caregivers. This program aims to enhance cognitive function, reduce cognitive and neuropsychiatric symptoms, decrease depressive symptoms, and improve health-related quality of life for both patients and caregivers. The study also examines the impact on the relationship quality between the care dyads compared to usual care. The intervention includes two phases: an active phase lasting 12 weeks and a maintenance phase lasting 6 weeks. During the active phase, care dyads participate in three small-group online sessions and three check-up/support sessions, alongside self-practice at home for at least 30 minutes a day, five times a week. The maintenance phase involves three additional online sessions and continued self-practice following the same schedule. Participants in the control group receive basic education on dementia caregiving through three group-based online meetings aligned with the intervention group's schedule. Participants will be assessed at baseline, 12 weeks, and 18 weeks for health-related quality of life, global cognition, and relationship quality. Additional evaluations include memory function, processing speed, executive function, behavioral and psychological symptoms of dementia, expressed emotion, caregiver burden, and compliance with sport stacking practice. The study is randomized and single-blinded, with ongoing monitoring of participant adherence and progress throughout the study period.

CONDITIONS

Brief Title

Dyadic Sport Stacking Program for Mild Dementia and Their Family Caregivers

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • People living with dementia (PLwD) with a clinical diagnosis according to DSM-V
  • People living with dementia aged 60 years or older
  • Clinical Dementia Rating (CDR) score of 1
  • Home-dwelling individuals
  • Able to communicate and understand training and assessments
  • Adequate hearing and visual function for skill learning
  • Provided informed consent
  • Family caregivers aged 18 years or above
  • Caregivers living with or providing care to PLwD at least 4 hours per day
  • Caregivers able to understand and communicate in Chinese
  • Caregivers have access to and use a smartphone, iPad, or laptop
  • Caregivers consent to participate
Not Eligible

You will not qualify if you...

  • People living with dementia with severe mental and behavioral disorders
  • People living with dementia with any acute medical condition preventing participation (e.g., pneumonia, cardiac insufficiency)
  • People living with dementia concurrently participating in other studies
  • Family caregivers physically unable to participate in sport stacking due to physical problems
  • Family caregivers suffering from acute psychotic conditions
  • Family caregivers unable to support the PLwD during sport stacking sessions

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 - 18 weeks

Participants engage in either an 18-week program of dyadic empowerment-based sport stacking with online group sessions and home practice, or receive basic education on dementia caregiving through online group meetings.

6 online group sessions over 18 weeks (weeks 1, 3, 9, 13, 16, and 18)

Trial Site Locations

Total: 1 location

1

the First Affiliated Hospital of Chongqing Medical University

Chongqing, China

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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