Actively Recruiting
An Implementation Science Approach to Evaluating Self-Administered Acupressure for Knee Osteoarthritis in Older Adults in the Community
Led by The Hong Kong Polytechnic University · Updated on 2026-01-09
368
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the use of a self-administered acupressure (SAA) program to manage knee osteoarthritis (OA) in older adults aged 60 and above in Hong Kong community centers. This pragmatic cluster randomized controlled trial aims to study how well the program is adopted, implemented, and maintained in real-world settings, and to assess its effectiveness in reducing knee pain, improving function, and enhancing quality of life. The study uses a mixed-methods approach, including qualitative interviews to explore the experiences of participants and service providers. Participants are divided into two groups: one receives the SAA program involving two 2-hour training sessions spaced one week apart, including acupressure techniques, knee health education, and practice with feedback. They are asked to perform acupressure at home twice daily for 24 weeks, with ongoing support through phone calls and messaging apps. The control group receives a general health education booklet and instructions to read it at home. After 24 weeks, the control group will also be offered the SAA program. During the study, participants undergo assessments at baseline and at weeks 4, 12, and 24, measuring knee pain severity using a numerical rating scale, knee function with the WOMAC index, quality of life with SF-6D, and physical function tests like Timed Up and Go and Fast Gait Speed. Researchers will monitor adherence, analgesic use, and implementation success through the RE-AIM framework. Data analysis includes quantitative comparisons and thematic analysis of interviews to understand facilitators and barriers. The total participation time spans 24 weeks with regular follow-ups.
CONDITIONS
Brief Title
An Implementation Science Approach to Evaluating Self-Administered Acupressure for Knee Osteoarthritis in Older-Aged Adults in the Community
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ethnic Chinese
- Aged 60 years or above
- Able to read Chinese and understand Mandarin or Cantonese
- Meet at least 3 clinical criteria for knee osteoarthritis (morning stiffness, crepitus, bone tenderness, bone enlargement, or no joint warmth)
- Have knee pain lasting at least 3 months
- Have a knee pain score of 3 or higher on a 1-10 scale
- Have access to a smartphone compatible with WhatsApp (self or family member)
- Willing to provide informed consent
You will not qualify if you...
- Medical conditions that prevent active participation (e.g., bleeding disorders, substance abuse)
- Knee pain caused by other conditions like cancer, fracture, rheumatoid arthritis, or rheumatism
- Cognitive impairment indicated by a score below 22 on the Hong Kong Montreal Cognitive Assessment
- Body mass index over 30
- Previous knee replacement surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 24 weeks
Participants in the acupressure group attend two training sessions to learn self-administered acupressure for knee osteoarthritis, followed by daily home practice twice a day with ongoing support.
2 training sessions (in-person) and daily home practice with phone and messaging support
Duration - 24 weeks
Participants are followed up and assessed at weeks 4, 12, and 24 for knee pain, function, quality of life, and compliance with the intervention.
3 follow-up visits (in-person) at Weeks 4, 12, and 24
Trial Site Locations
Total: 1 location
1
The Hong Kong Polytechnic University
Kowloon, Hong Kong
Actively Recruiting
Research Team
W
Wing-Fai YEUNG, PhD
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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