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NCT07786038Not yet recruiting

E-Health Lifestyle Intervention for Arthritis: A Pilot RCT on Feasibility

Community Healthy Asian Lifestyle for Ameliorating Arthritis With Navigational E-health: A Pilot Randomized Controlled Trial on Feasibility and Acceptability

Source: ClinicalTrials.gov · Last updated 25 Aug 2026

Brief summary (registry, in English)

Knee osteoarthritis and obesity are common health problems in Hong Kong, especially among South Asian communities, where obesity rates are much higher than the general population. These two conditions often make each other worse-pain from arthritis leads to less physical activity, which can lead to more weight gain and more joint pain. This pilot study is testing a new digital health program called CHALAANE(Community health asian lifestyle for ameliorating arthritis with navigational e-health), which means "walk" in Hindi and Urdu. The program uses a smartband and a mobile app with artificial intelligence to help participants track their activity and diet. It also includes a 12-week supervised program with group walking sessions and lifestyle education. The study will include 50 South Asian adults aged 40 to 75 years who have knee osteoarthritis and obesity. Participants will be randomly assigned to one of two groups. The intervention group will receive the full CHALAANE program with an activated smartband and mobile app. The control group will receive an inactivated smartband for activity monitoring only. The study will last 10 months, with assessments at multiple time points. The main goal of this pilot study is to see if a larger future study would be feasible. The researchers will measure how many participants follow the program as instructed and how many complete the full 10-month study. They will also look at whether the program is acceptable to the South Asian community and gather early data on pain, physical function, and body composition. The study is a collaboration between the Department of Orthopaedics \& Traumatology at Queen Mary Hospital and The Duchess of Kent Children's Hospital. A total of 50 participants will be recruited. Results will help inform the design of a future full-scale trial to improve health outcomes in this underserved population.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
17 Aug 2026
Start date
1 Sept 2026
Primary completion date
31 Dec 2028
Lead sponsor
The University of Hong Kong
Diseases
Obesity
NCT number
NCT07786038

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 1 Sept 2026 to the primary completion date, 31 Dec 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous knee surgery

Other illness

  • cognitive impairment, vision and hearing impairment precluding use of Smartband+App

Other

  • Unwillingness/inability to change eating/physical activity habits
  • Severe knee OA daily resting pain (NPRS\>8/10) or (Kellgren-Lawrence grade=4) that could not tolerate further conservative management
  • inflammatory arthritis like rheumatoid arthritis, etc.
  • immediate requirement for joint replacement, e.g. bone loss
  • Planning to leave HK \>2 months during the study period
  • losing/gaining \>5% weight in 6months or on dieting
  • high levels of psychological distress (Kessler 10 questionnaire-K10 score \>29)

Who the study is looking for

  • Inclusion criteria:
    • South Asian
    • Men and women aged 40 to 75 years, with obesity (body mass index≥25 kg/m2, Hong Kong Centre for Health Protection obesity definition)
    • Knee osteoarthritis (European League Against Rheumatism (EULAR) clinical criteria): age≥40 with movement-related joint pain, morning knee stiffness\<30 min, and functional limitations, and crepitus/reduced range/bony enlargement)
    • Pain less than 2 years

Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Queen Mary Hospital
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status
The Duchess of Kent Children's Hospital at Sandy Bay
Coordinator of this site? Confirm its status
Hong KongHong Kong SAR ChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.