Integrating SPOZ Technology to Support and Enhance the Vitality Acupunch (VA) Exercise Program for Older Adults With Dementia
The Integration of SPOZ Technology to Support and Enhance the Vitality Acupunch Exercise Program for Improving the Disease Dysfunction and Functional Fitness Deterioration of Older Adults With Dementia
1 other identifier
interventional
142
1 country
1
Brief Summary
This project was aimed to examine the effects of a six-month VA exercise program incorporated the SPOZ technology in improving the disease dysfunction and functional fitness deterioration of older adults with dementia in adult daycare centers.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 17, 2025
CompletedFirst Posted
Study publicly available on registry
April 24, 2025
CompletedStudy Start
First participant enrolled
April 24, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 18, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 18, 2025
CompletedDecember 24, 2025
December 1, 2025
8 months
April 17, 2025
December 18, 2025
Conditions
Outcome Measures
Primary Outcomes (8)
Balance
measured by the Balance tests in SPPB
6 months
Lower muscle endurance
measured by the 5-time sit-to-stand in SPPB
6 months
Gait speed
measured by the 4-m walk in SPPB
6 months
Handgrip strength
measured by the Digital Handgrip Dynamometer (TKK-5101)
6 months
Cardiorespiratory endurance
measured by the 2-minute step test
6 months
Muscle endurance
measured by the SPOZ devices
6 months
Agility
measured by the SPOZ devices
6 months
Body flexibility
measured by the SPOZ devices
6 months
Secondary Outcomes (3)
Activities of daily living (ADL)
6 months
Instrumental activities of daily living (IADL)
6 months
Sleep quality
6 months
Study Arms (2)
VA-SPOZ exercise program
EXPERIMENTALThe VA-SPOZ exercise program was comprised of 3 parts: (1) the first part had 5 movements, including breathing regulation, alternating arm stretching, trunk movement, alternating left and right legs, and gradually started the blood circulation in a gentle way; (2) the second part had 14 movements, using five punching techniques, the left and right arms alternating in a natural parabola, and punching the acupoints to vibrate meridians. The purpose of the second part of the movement was to stimulate the 14 meridians and to promote the circulation of qi and blood throughout the body; (3) the third part had 5 movements, which were to adjust the breath, relax the muscles, stretch the body, and warm the face and lower back of the body by hand touch. Participants wore SPOZ devices on both hands to record and track the accuracy of the movements.The 40-minute program was administered three times a week for 6 months.
Control
ACTIVE COMPARATORParticipants in the control group maintained their routine activities.
Interventions
The VA-SPOZ exercise program had 3 phases and took 40 minutes to complete. The program was performed in a seated position, and the participants wore SPOZ devices on both hands to record and track the accuracy of the movements.
Eligibility Criteria
You may qualify if:
- diagnosed as dementia by a physician, or
- screened by the SPMSQ as dementia
- age 65 and older
You may not qualify if:
- have severe cardiopulmonary disease
- have physical mobility impairment
- have spinal cord injury
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Kaohsiung Medical University
Kaohsiung, Taiwan, 80708, Taiwan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kuei-Min Chen, PhD
Kaohsiung Medical University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
April 17, 2025
First Posted
April 24, 2025
Study Start
April 24, 2025
Primary Completion
December 18, 2025
Study Completion
December 18, 2025
Last Updated
December 24, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share