Can a smartband and AI app ease knee pain and obesity?

NCT ID NCT07786038

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Aug 25, 2026 · Last updated Aug 26, 2026 · Updated 1 time

Summary

This pilot trial is testing a digital health program called CHALAANE, which means 'walk' in Hindi and Urdu, for South Asian adults with knee osteoarthritis and obesity. The program combines a smartband, an AI-powered mobile app for tracking diet and activity, and a 12-week supervised group walking and lifestyle education component. The study will include 50 participants aged 40 to 75, randomly assigned to either the full program or a control group with an inactive smartband. The main goal is to see if a larger study is feasible, while also gathering early data on pain, physical function, and body composition.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A digital health program combining a smartband, an AI-powered mobile app for diet and activity tracking, and a 12-week supervised group walking and lifestyle education component.
What this could lead to
If successful, this program could offer a practical, culturally tailored way to help South Asian adults with knee osteoarthritis and obesity improve pain, physical function, and weight management.
What could go wrong
This is a small pilot study focused on feasibility, not proof of effectiveness. The program may not be acceptable or feasible for all participants, and any benefits seen may not persist or generalize to a larger population.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 50 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

May 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

40 to 75 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Inclusion criteria: 1. South Asian 2. Men and women aged 40 to 75 years, with obesity (body mass index≥25 kg/m2, Hong Kong Centre for Health Protection obesity definition) 3. 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) 4. Pain less than 2 years Exclusion Criteria: 1. Unwillingness/inability to change eating/physical activity habits 2. Severe knee OA daily resting pain (NPRS\>8/10) or (Kellgren-Lawrence grade=4) that could not tolerate further conservative management 3. inflammatory arthritis like rheumatoid arthritis, etc. 4. Previous knee surgery 5. immediate requirement for joint replacement, e.g. bone loss 6. Planning to leave HK \>2 months during the study period 7. cognitive impairment, vision and hearing impairment precluding use of Smartband+App 8. losing/gaining \>5% weight in 6months or on dieting 9. high levels of psychological distress (Kessler 10 questionnaire-K10 score \>29)

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

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  3. A doctor treating you

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Contacts and locations

Locations

  • Queen Mary Hospital

    Hong Kong, Pofuklam, 999077, Hong Kong

  • The Duchess of Kent Children's Hospital at Sandy Bay

    Hong Kong, Sandy Bay, 999077, Hong Kong

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