Actively Recruiting

Phase Not Applicable
Age: 60Years +
All Genders
ID07329023

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

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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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)

Training and Treatment

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

Follow-up and Outcome Assessment

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

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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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